Next Article in Journal
Prp19 Arrests Cell Cycle via Cdc5L in Hepatocellular Carcinoma Cells
Previous Article in Journal
The Effect of Low-Dose Proteasome Inhibition on Pre-Existing Atherosclerosis in LDL Receptor-Deficient Mice
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
IJMS
Volume 18
Issue 4
10.3390/ijms18040789
ijms-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Advances in Skin Regeneration Using Tissue Engineering

by
Komal Vig
*,
Atul Chaudhari
,
Shweta Tripathi
,
Saurabh Dixit
,
Rajnish Sahu
,
Shreekumar Pillai
,
Vida A. Dennis
and
Shree R. Singh
Center for Nanobiotechnology Research, Alabama State University, 1627 Harris Way, Montgomery, AL 36104, USA
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2017, 18(4), 789; https://doi.org/10.3390/ijms18040789
Submission received: 9 February 2017 / Revised: 4 April 2017 / Accepted: 4 April 2017 / Published: 7 April 2017
(This article belongs to the Section Materials Science)
Browse Figures
Versions Notes

Abstract

:
Tissue engineered skin substitutes for wound healing have evolved tremendously over the last couple of years. New advances have been made toward developing skin substitutes made up of artificial and natural materials. Engineered skin substitutes are developed from acellular materials or can be synthesized from autologous, allograft, xenogenic, or synthetic sources. Each of these engineered skin substitutes has their advantages and disadvantages. However, to this date, a complete functional skin substitute is not available, and research is continuing to develop a competent full thickness skin substitute product that can vascularize rapidly. There is also a need to redesign the currently available substitutes to make them user friendly, commercially affordable, and viable with longer shelf life. The present review focuses on providing an overview of advances in the field of tissue engineered skin substitute development, the availability of various types, and their application.

1. Introduction

Skin is the barrier between the internal and external environment and is the largest organ of the human body. Due to the presence of stem cells, the wounded epidermis is able to stimulate self-regeneration. However, in case of deep injuries and burns, the process of healing is not adequate, thus leading to a chronic wound. Any loss of full-thickness skin more than 4 cm diameter needs grafting for its treatment [1]. Additionally, many chronic wounds fail to heal, which can lead to amputations and mortality. These can also escalate health care costs. Surgical procedures available for skin healing often have limited availability of healthy donor tissue. The use of foreign tissue does provide a substitute; however, it also poses a risk of infection and immune rejection.
Tissue engineered skin substitutes are upcoming alternatives to traditional wound healing strategies and tissue regeneration. Among the tissue engineered organs, skin was the first engineered organ that went from laboratory research to patient care [2]. Over recent decades, various bioengineered and synthetic substitutes have been developed, which are generally positioned within the injury and provide the barrier function along with protection against microorganisms, reduction of pain in wounds, and promotion of wound healing by tissue regeneration [3,4,5].
The field of tissue engineering is an evolving field, and newer procedures are being developed and adopted to generate skin substitutes for clinical applications, even though the high cost for developing these substitutes is a major concern. The current review highlights the progress in the field of tissue-engineering and investigates various commercially available skin substitutes along with their advantages and shortcomings.

2. Anatomy of Skin

The skin is the largest organ of the body. It compromises 15% of the total adult body weight and provides protection against external physical, chemical, and biologic agents. It also plays role in thermoregulation. Skin consists of three layers: epidermis, dermis, and hypodermis (subcutaneous layer) (Figure 1). The outermost portion of the epidermis, the Stratum corneum, is comparatively more waterproof than other layers and thus inhibits entry of pathogens and other foreign substances into the body. It is multi-layered, with cells extending from the basement membrane to the dermis. The basement membrane contains progenitor cells, which differentiate into keratinocytes. Keratinocytes differentiate and mature as they move towards the surface of skin. The keratinized layer of dead cells at the skin provides barrier properties to skin [6]. Skin color pigment, melanin produced by melanocytes, are present in basal layer of the epidermis. Melanin also helps to filter out ultraviolet radiation from sunlight. The epidermis also has Langerhans cells, which are part of the skin’s immune system.
The dermis is the thickest of the three layers of skin and is present just below the epidermis. It is a connective tissue made of extra cellular matrix (ECM), fibroblasts, vascular endothelial cells, along with hair follicles, sweat glands, sebaceous glands, blood vessels and nerve endings [6]. Fibroblasts are the main population of the dermis, which secretes collagen and elastin and thus provides mechanical strength and elasticity to the skin.
Below the dermis is the adipose tissue hypodermis layer. It provides insulation and cushioning between the skin and skeletal structures, such as bone and muscle. It also serves as an energy storage area [6].

3. Wounds

Each year in the United State alone, there are 70,000 burn injuries [7] and 600,000–1,500,000 venous leg ulcers injuries [8]. The treatment of wounds costs nearly $20 billion annually in the US [9].
Wound treatment mainly includes quick closure of wound to reinstate the barrier function of skin and prevent infection, along with pain suppression and functional recovery. Wound healing in skin is initiated by fibroblasts, which deposit a temporary tissue matrix. This is followed by inflammation and re-epithelization by keratinocytes. Further wound revascularization along with ECM deposition, angiogenesis, and remodeling takes place for wound healing and restoration [6,10].
Every trauma often results in acute skin wounds. After the repair process, these wounds often lead to a benign scar if not treated in time [11]. However, depending upon the extent of the wound area and/or depth, sometime, a chronic or non-healing wound can also result. Wounds that do not proceed through orderly and timely restitution of structural and functional integrity often results in chronic wounds. Generally, vascular insufficiency, local-pressure effects, and conditions like diabetes mellitus, along with compromised nutritional or immunological status, are the major causes of non-healing skin wounds. Healing capability of a wound is affected by aging, which leads to decreased strength and elasticity of skin, decreased blood flow to the extremities, and psychological stress [12,13].

4. Process of Skin Wound Healing

After a skin injury, the damaged tissue is restored through coordinated signaling that constitutes the cutaneous healing response. This cutaneous response proceeds in three phases: the inflammatory phase, proliferation phase, and maturation phase. The inflammatory phase of wound healing typically lasts for the initial four days [14] and begins with coagulation of blood resulting in a blood clot that provides a temporary shield against pathogens as well as fluid loss. It is followed by increased blood flow in the areas adjacent to the wound trailed by swelling and redness due to increased vascular permeability by local inflammatory agents (activated complement, histamine, etc.) leading to plasma extravasation and generation of a fibrin matrix [6]. Neutrophils, monocytes, and other immunocompetent cells invade this matrix to remove dead tissue and control infection.
After the inflammatory phase, between 5–20 days, proliferation of vascular endothelial cells and fibroblasts is promoted due to secretion of growth factors by inflammatory cells. Fibrin matrix is gradually replaced by collagen secreted by fibroblasts. Fibroblasts can differentiate into myofibroblasts expressing actin resulting in contraction and reduction of the wound area. Adjacent healthy tissue, as well as endothelial progenitors, initiate angiogenesis, which leads to invasion of vascular endothelial cells and capillaries, resulting in the formation of “granulation tissue” [6]. It is followed by migration of keratinocytes from the edges of the wound to the surface of the granulation tissue, below the blood clot [14].
During the last phase of maturation, re-epithelialization of the wound takes place along with dermis regaining its tensile strength. However, the scar continues to remodel over several months to years [6].

5. Conventional Treatments for Wound Healing

Different strategies have been employed for wound treatments, which are discussed below:

5.1. Skin Grafting with Autograft

Due to lack of keratinocytes to reform the epithelium, deeper dermal wounds heal slowly and inadequately. Skin grafting with an “autograft” is recommended for such wounds [15]. Skin autograft technique was used in India in premodern times [16]. A thin layer of skin that includes the full epidermis and a portion of the dermis, known as split-thickness graft, is shaved from the donor site, such as inner thighs and buttocks, using a dermatome, and is then placed on the wound site [17]. The healing of wound depends on thickness of the underlying dermis in the graft. Thick dermis leads to faster healing and better cosmetic and aesthetic aspect of the healed wound. Donor sites can be reharvested a few times after healing, as the sites thin down due to lack of regeneration of the dermis after each harvest. Since an autograft is derived from the patient’s own tissue, there is no risk of rejection [15].

5.2. Skin Allografts

A method to overcome the limitation of donor tissue for skin grafting with an autograft is to use allografts. Human skin allograft clinical use was first described in the manuscript of Branca of Sicily in 1503. Skin allografts have been used since World War II.
Cadavers are a good source of allografts. As cadavers are stored frozen in skin banks, they can be used as needed [18]. Allografts from cadavers are used extensively in burn wound management in many burn centers all over the world. Skin allografts can also be obtained from living donors.
A viable skin allograft can revascularize like autologous split skin grafts. Though allografts not only provide a barrier along with promoting angiogenesis, providing growth factors, and essential cytokines for wound healing [19], they also serve as a temporary cover due to immunogenic rejection by the host’s immune system [15,20] and viral transmission (e.g., hepatitis B and C or HIV). Application of human skin allograft guards underlying tissue while allowing granulation tissue formation and wound contraction. Subsequent skin autograft and secondary skin contraction and epithelialization provide satisfactory wound closure [21].

5.3. Xenografts

A surgical graft from one species to another dissimilar species is known as xenograft. Skin substitutes harvested from the animals that are used on human wounds constitute xenograft and can be used as temporary grafts for human wounds. Xenograft fuses exogenous collagen into the wound, thus assisting dermal regeneration. These xenografts get absorbed as the wound heals, thus making them perfect for surgical wounds [22]. Skin xenograft was reported in the Papyrus of Ebers in the 15th century BC [19]. The earliest reported xenograft was with frog skin in 1500 BC. These are usually employed as temporary coverage [23]. Most commonly used xenografts are from porcine skin, which is often used in burn care [19].

5.4. Amnion

Since 1910, amnion has been used as a dressing for burns [19]. Amnion is primarily used for partial thickness burns, such as facial burns, and is one of the most effective biological skin substitutes [24]. Amnion is also used in sandwich grafting technique. Amnion is usually collected from the placentae of selected and screened donors and preserved for further use. It reduces loss of protein, electrolytes, and fluids, minimizes pain, decreases the risk infection, and accelerates wound healing. In a recent clinical trial, amnion dressing was used for the donor site on 32 patients, which resulted in fast epithelialization and wound healing [25], thus, improving pain, through use of less analgesics, low rate of immobilization, and resulted in the earlier discharge of patients. Amniotic membrane is rich in collagen and several growth factors that support the healing process to both advance wound closure and diminish scar formation. Its distinctive properties include the lack of immunologic markers, antibacterial properties, and the ability to reduce pain on application. Recently, techniques have been developed to dehydrate the amnion while preserving many of these wound-healing attributes, to produce a temperature-stable allograft [26].

6. Newer Approaches for Tissue Engineering

Different strategies, such as injecting growth factors and extracellular matrix, are being adopted towards tissue re-growth and wound healing. Some of the recent strategies are listed below.

6.1. Cell Cocultures

Cell-based approach to develop skin substitutes usually involves differentiated, embryonic, or induced pluripotent stem cells. Cells such as human dermal fibroblasts [27], foreskin derived keratinocytes [28], keratinocyte stem cells [29], hair follicle stem cells [30], angiogenic endothelial progenitor cells [31], bone marrow-derived mesenchymal stem cells [32], and adipose tissue derived mesenchymal stem cells [33] are mainly used for wound healing and tissue regeneration. Work is progressing toward co-culturing cells for tissue generation that involves keratinocytes and fibroblasts [34,35]. Keratinocyte sheets of stratified epithelia can be reconstructed from human epithelial cells [36,37]. Moreover, cultured dermal substitutes containing fibroblasts can be added to keratinocytes sheets. Fibroblast cells can stimulate keratinocyte growth and differentiation by either secreting soluble growth factors or via cell–cell contacts and cell matricial element contacts. In turn, keratinocytes can positively affect fibroblast proliferation [38]. Dermal fibroblasts are also important in skin remodeling and acute wound contraction [39]. Melanocytes and Langerhans’ cells can also be cultured along with keratinocytes and fibroblasts. Melanocytes can recreate the natural pigmentation process whereas Langerhans’ cells monitor skin immunological reactions. Recently, complex three-dimensional (3D) models are being developed using these co-cultured cells with the goal of making engineered tissues similar to their natural counterparts. An exclusive full-thickness 3D skin equivalent was developed to model early melanoma invasion by incorporating an inert scaffold with suitable pore sizes to support the 3D development and cell–cell interaction of primary human dermal fibroblasts [40].

6.2. Cultured Epithelial Autografts

Epithelial autografts are used in burn care [41,42] and were first reported in clinical use in 1981. These autografts can be constructed using keratinocytes. Keratinocytes were first cultured successfully in the laboratory about 30 years ago [43,44]. Keratinocyte cells can be generated from a small biopsy of healthy skin, expanded into sheets for few weeks, which is then co-cultured on mouse fibroblasts [45,46]. Epithelial autografts are, however, limited due to difficulty of handling, unpredictable uptake, and high cost, and thus need a delivery system or a support dressing.

6.3. Tissue Engineered Skin Substitutes

Due to deficiency of donor skin graft supplies, tissue-engineered skin substitutes present an efficient alternative in substituting donor skin grafts. Skin substitutes are emerging therapeutic tools with a wide range of applications. Skin substitutes act as a temporary protective cover of the wound bed, thus protecting damaged regions from fluid loss and contamination along with accelerating the wound-healing processes by promoting release of cytokines and growth factors at the wound site [47].
An absorbent dressing made of cotton wool sandwiched between layers of gauze was described by Joseph Gamgee in 1880 and used as “skin substitutes” for treating wounds [48]. Likewise, in 1895, Mangoldt described a technique of “epithelial cell seeding” for treating chronic wounds [45]. His technique involved harvesting epithelial cells from superficial epithelium of skin and seeding them onto the wounds [49]. Similarly, in 1897, Lunggren kept skin fragments alive by inoculating them in ascitic fluid at room temperature [45,50]. Likewise, keratinocytes were grown successfully on lethally irradiated murine fibroblasts [43,45]. Cultured autologous epithelium was used to cover burn defects for the first time by O’Conner [42,48]. Likewise, a dermal substitute was developed based on collagen gel with fibroblasts to which an epidermal layer was added, thus making a “skin equivalent”, “composite culture”, or “organotypical culture” [45,50].
Tissue engineered skin substitute preparation involves cells and/or extracellular matrix (ECM) [18] (Figure 2). An ideal synthesized skin substitute should be sterile, act like a barrier, have low inflammatory response, provide no local or systemic toxicity, and allow water vapor transmission similar to normal skin. These skin substitutes should also adhere to wound surface rapidly, have required physical and mechanical properties, and go through controlled degradation [51]. They should also be easy to handle, agile to conform to irregular wound surfaces, relatively inexpensive, and facilitate angiogenesis. They should also have a long shelf-life with low storage requirements and stress resistance in engineered skin substitutes [52]. When biomaterials are used for substitutes, they should be biodegradable, repairable, non-toxic, non-immunogenic, and non-inflammatory with low risk of disease transmission. Easy availability, long-shelf life, and user-friendliness makes an ideal engineered substitute. A suitable biomaterial is crucial in the development of functional engineered tissues. Different approaches have been adopted to develop engineered tissues, such as synthetic membranes for mono- or multi-layered cultures and 3D matrices for full-thickness models. Properties of the “ideal” skin substitute for in vivo use have recently been reviewed by MacNeil [51].
Tissue engineered skin provides both epidermal and dermal components required to achieve functional wound closure and have therefore been used to effectively close full-thickness burn wounds and treating burns that are greater than 50% of the total burn surface area (TBSA) [7,46,53,54]. The presence of a large number of cells, especially stem cells, in tissue engineered skin enables regeneration of native-like skin in burn patients.
Tissue engineered skin is mainly of three types: (a) cultured epidermal cells with no dermal components; (b) with only dermal components; or (c) a bilayer containing both dermal and epidermal components [55]. Although, each of these has their own advantages and applications, none of them can fully simulate native skin.

7. Types of Skin Substitutes

Currently, available skin-substitutes can be classified in different ways [4,49,51,55,56,57]. Based on duration of cover, they are classified as permanent, semi-permanent or temporary. Based on anatomical structure, they are classified as epidermal, dermal, or dermo-epidermal (composite). They can also be classified based on skin substitute composition as cellular or acellular. Similarly, based on the type of the biomaterial used, they can be biological (autologous, allogeneic, xenogeneic) or synthetic (biodegradable, non-biodegradable).
Synthetic skin substitutes are made up of acellular materials. They are designed primarily to function as barriers to fluid loss and microbial contamination. Commonly used synthetic acellular skin substitutes are Biobrane®, Integra®, Alloderm™, and TransCyte™. The natural skin substitutes, commonly called tissue engineered skin, are mainly cultured allogenic or autologous cell suspensions or sheets, which are used on their own or along with a dermal matrix. Examples of frequently used natural skin substitutes with allogeneic cells include Dermagraft™, Apligraf™, and OrCel™, while those with autologous cells include Epicel™ (Table 1). These substitutes are further described below.

7.1. Acellular Skin Substitutes

The use of acellular skin substitute started in late 1970s and is used mainly as a temporary skin substitute for superficial or mid-dermal partial thickness wounds and burns. They can also be used for donor sites and congenital diseases, such as epidermolysis bullosa [58,59] and in hydradenitis suppurativa [60]. They usually consist of a nylon mesh or collagen, acting as a “dermis” and a silicon membrane as an “epidermis”. There are three kinds of commercial available acellular skin substitutes: Biobrane®, Integra®, and Alloderm (Figure 3a). Details about their composition are in Table 1.

7.2. Cellular Allogenic Skin Substitutes

Cellular allogenic skin substitutes are mainly produced using living neonatal foreskin fibroblasts with a mesh or a matrix. They have been used successfully in vestibuloplasty, after mucogingival junction and supra-periosteal dissection [46,49]. They have also been used for treatment of venous and diabetic ulcers along with wound management in epidermolysis bullosa, skin cancer, and in burns [46,49]. Examples include Transcyte®, Dermagraft®, Apligraf®, and Graftskin® (Figure 3d,f,g).

7.3. Cellular Autologous Skin Substitutes

Acellular or cellular allogenic skin substitutes only provide temporary coverage to raw skin surfaces. These have to be either replaced by a split skin graft or re-grafted in the case of large wounds. In the case of smaller wounds, gradual epithelialization from the wound itself is required.
Cultured autologous keratinocytes provide more permanent skin coverage for various types of wounds. These cells are cultured based on the Rheinwald and Green [43,44] technique. There are two types of cellular autologous skin substitutes available: Cultured Epidermal Autograft (CEA) and Cultured Skin Substitutes (CSS).
CEA involves the culture of autologous keratinocytes, derived from skin biopsy of the patient [45,46]. However, after few weeks, it is challenging to handle these keratinocytes, thus requiring a delivery system or a supporting dressing [48,49]. Commercially available CEAs have different delivery or carrier systems. Keratinocytes alone may not heal full thickness wounds or burns. Another concern with CEA is the growth of blisters with friction, since their dermal epidermal junction is not completely developed. It can also lead to increased scarring, contracture and hyperkeratosis [46]. Furthermore, due to the digestive properties of collagenase enzymes within the wound bed, the uptake of CEA is reduced to about 30%–80%. To overcome the issue of CEA uptake, an alternate method was developed [18,48], which included acclimatization of the wound bed with cadaveric allogenic skin for four days before grafting followed by placing autologous cells after stripping the allo-epidermis [18,48].
CSS is an autologous graft with both epidermal and dermal components. It acts as a permanent coverage with well-formed dermal-epidermal junction and is easy to handle. CSS is expensive and has a longer preparation time. [18,46,49]. Different dermal biosynthetic scaffolds are being used to develop several types of CSS. Hyaluronic acid derived substitute is often used to prepare CSS. These types of CSS can stimulate fibroblasts growth and movement, controls osmoregulation and matrix hydration, scavenge free radicals and regulate inflammation [61,62].

7.4. Commercially Available Skin Substitutes

There are many commercial skin substitutes, permanent or temporary, that are available in the market designed for use with specific clinical issues [19,22,51,55,63,64]. Commercially available engineered skin substitutes’ models vary in techniques and cell sources (Figure 3). Table 1 lists some of the commercially available skin substitutes.
Skin substitutes like Biobrane®, Integra®, and Alloderm are made of acellular material, such as a nylon mesh or collagen (Figure 3a). Biobrane® and Integra® are synthetic bilayer skin substitutes. Biobrane® is made of a nylon mesh mimicking as a “dermis” and a silicone membrane as an “epidermis” implanted in porcine collagen [46,49,55]. Integra® consists of a silicone membrane as an epidermal layer and dermal layer made of bovine collagen and shark chondroitin-6-sulphate glycosaminoglycan [18,46,49]. Although, Biobrane is used for covering partial thickness burns in a single stage procedure, it has the drawback of being intolerant to contaminated wound beds. Integra, on the other hand, has good long term aesthetic and functional outcome, but is a two stage process with high cost and poor adhesion [97,98,99,100]. Integra may also include a high vulnerability to infection, graft loss and fluid entrapment, requiring fenestration of the tissue. Another substitute that falls in this category is Advanced Wound Bioengineered Alternative Tissue (AWBAT) [22,101], which is made of porous silicone membrane bonded with a continuous 3D nylon structure that contains non cross–linked porcine type 1 collagen peptides.
Alloderm, Graftjacket, and GammaGraft are allografts derived from an acellular matrix obtained from a cadaveric dermis [22]. As a decellularized tissue-engineered skin substitute, alloderm consist of a cell-free matrix incorporated into the wound bed [65]. It has a basement membrane but lacks an epidermal layer. The acellular matrix provides a good natural medium for fibroblast and endothelial cells to regenerate from the neoderm [18,46,49]. It is immunologically inert and offers natural dermal porosities for renewal and vascularization on the wound bed, but has the drawback of being a two stage very expensive technique with a risk of transmitting disease [51,91,102,103].
Other commercial skin substitutes such as ApligrafTM, CeladermTM, DermagraftTM, TrancyteTM, and OrCelTM (Figure 3), are constructed from sheets of cells derived from neonatal (allogenic) foreskin [19,63,92,93]. TransCyte™ has similar configuration to Biobrane® and consists of a nylon mesh seeded with fibroblasts cultured from neonatal human foreskin. The foreskin secretes ECM components and growth factors for efficient tissue regeneration. It is often used as a temporary cover for excised burns and considered more beneficial for wound healing compared to strictly synthetic skin substitutes [81,104]. Transcyte has the advantage of immediate availability and easy storage but is only a temporary solution.
Dermagraft, on the other hand, is an allogeneic dermal substitute created by the combination of living neonatal foreskin fibroblasts cells and biodegradable mesh from polyglycolic acid biomaterials [105]. The fibroblasts are cryopreserved at −80 °C and when implanted to the wound, they regain their viability and proliferate and produce growth factors and ECM components [106]. The polyglycolic acid mesh is absorbed within 3–4 weeks [46,49]. Dermagraft is easy to handle with coverage to chronic wounds and diabetic ulcers with no rejection. However, it lacks strong ECM structure leading to infections and cellulitis [51,98,103].
Skin substitutes of composite allograft category include ApligrafTM and OrcelTM. ApligrafTM contain both living dermis and epidermis and is formulated by mixing living fibroblasts from neonatal foreskin with bovine collagen. This mixture is further exposed to heat to produce a loose matrix, which develops a dermal fibrous network. Cells are proliferated on the dense fibrous matrix [61]. In the treatment of venous leg ulcers and diabetic foot ulcers, Apligraf™ is often used [61]. Treating wounds with Apligraf for more than four weeks results in enhanced healing when compared with any other skin substitute currently available in the market. The downside of Apligraf is that it is rather expensive, with a short shelf-life (range: 5–10 days), and although the risk is significantly low, there is a likelihood of disease transmission owing to Apligraf being allogenic in nature [107,108]. Similar to ApligrafTM, OrCelTM is another skin substitute that is made up of fibroblasts seeded into a bovine collagen type I matrix (dermal side) and keratinocytes cultured at the air–liquid interface (epidermal side) [86,87,88]. It provides a favorable matrix for host cell migration and is used for grafting onto partial-thickness wounds; nonetheless, there is an amplified risk of rejection and disease due to the presence of the bovine collagen [52,107].
Other skin substitutes like Permacol, Matriderm, and Oasis belong to the xenograft category [79,85]. Permacol is made of porcine dermis, whereas Matriderm® is made of a matrix of bovine type I collagen with elastin (Figure 3e). It is utilized for dermal regeneration. With the progression of healing process, fibroblasts lay down the ECM and the Matriderm® resorbs [109]. Permacol has a good aesthetic and functional outcome but is prone to infection, hematomas, and seromas [73,74], whereas, Matriderm involves a single stage procedure with increased vascularization and elasticity of regenerating tissue but lacks enough scientific evidence to verify its efficacy of a one-step procedure [103,110,111]. Another substitute is Oasis, which is derived from porcine intestinal submucosa [79,85].
The commercially available CAE substitutes, such as Epicel™, are made of autologous keratinocytes sheets attached to a petrolatum gauze support, which is detached approximately one week after grafting [73]. Epicel™ is used on patients with full-thickness burns covering more than 30% total body surface area (TBSA). It is also used on patients with giant congenital nevus [73]. Epicel, however, has a longer generation time. It takes almost three weeks to culture the tissue for use. Since the tissue is an autograft, there is a very low risk of rejection [107,112].
Another variation of CAE substitutes is a suspension, such as Cell Spray (Figure 3b). Keratinocytes harvested in a suspension from a split-thickness donor biopsy is placed in the wound to create an epidermal cover. As the application is aerosolized, it allows complete coverage of contoured wounds [70,71,72,79]. The downside of this application is that there is a risk of infection or donor rejection [77,78,79].
Epidex is an additional CAE substitute, having small keratinocyte sheets cultured from patient’s follicles [67]. It can be expanded in vitro for large burn areas. Though it is a permanent substitute, it is also fragile and expensive [41,42]. Like Cell Spray CAE, subconfluent cells on a carrier make epithelial substitutes, such as Myskin (CellTran) [68].
Hyalograft 3D is another autologous dermal substitute. In this product, autologous cultured fibroblasts are seeded onto a 3D hyaluronic acid derived scaffold [79]. Hyalomatrix® is a bilayer hyaluronan base scaffold with autologous fibroblasts and an outer silicone membrane (Figure 3c). The silicone membrane acts as a temporary epidermal barrier and hyaluronan is delivered to the wound bed [84]. Laserskin is another autologous epidermal substitute [74]. Another similar substitute is TissueTech autograft system, which has been used in successful treatment of diabetic foot ulcers (Figure 3f) [80]. It combines two tissue-engineered biomaterials, a dermal replacement construct Hyalograft 3D and an epidermal substitute Laser skin [80]. In this system, autologous keratinocytes and fibroblasts are grown on micro perforated hyaluronic acid membranes. Up to 70.3% of wound closure with an area greater than 5 cm2 in 85% of cases was accomplished in many full-thickness ulcers using TissueTech autograft system [80]. The rate of recurrence was also low with this TissueTech Autograft System. Although this system may allow for absolute wound closure, it is not a “rue” bilayered skin substitute where both dermal and epidermal layers are present, as it entails grafting of two products and may be difficult to use in a clinical setting [80].
Other skin substitutes are based on fibroblasts seeded onto a synthetic polymer membrane [89], such as polylactic-glycolic acid (PLGA), polycaprolactone (PCL), a combination of PLGA/PCL, and mixtures made of hyaluronic acid (HA). Polypyrrole (PPy) can be used as a cultured dermal substitute [83]. PPy and HA, in particular, are reported to promote skin regeneration and cell growth. Polypyrrole (PPy) has good in vitro and in vivo biocompatibility and can be fabricated with a large surface area, with different porosities. However, PPy is very difficult to further process once synthesized, as its molecular structure makes it non-thermoplastic, mechanically rigid, brittle and insoluble after synthesis [113,114,115].
An allogenic living epidermal substitute such as Stratagraft is a full thickness skin substitute consisting of human dermal fibroblasts as a dermal component and neonatal keratinocytes as a fully-stratified epidermis [79,94,95,96]. It serves as a bridge before autografting in burn patients and other severe skin wounds. Stratagraft is well-tolerated and is not acutely immunogenic in patients with traumatic wounds [87].
Alternative skin substitute Permaderm™ contains both epidermal and dermal components composed of autologous fibroblasts and keratinocytes cultured on a collagen substrate. It has the advantage of being a one-step procedure with permanent replacement of dermal and epidermal layers. However, no clinical trials have been reported yet [46,116,117,118,119,120]. Another full thickness skin substitute that is used in chronic therapy-resistant leg/foot ulcers is Tiscover™. Similarly, DenovoDerm™ and DenovoSkin™ are also full-thickness dermal skin substitutes that are currently undergoing trials. Denovoskin has a near normal skin architecture but has long culture times with no clinical series yet reported [7,51]. However, each of these products has its own limitations, and there is no perfect or ideal skin substitute yet [78].

8. Limitations of Commercially Available Skin Substitutes

There are several limitations to the commercially available skin substitutes, like reduced vascularization, poor mechanical integrity, failure to integrate, scarring, and immune rejection [51]. Due to the inability to revascularize, cells in the substitute die and slough away from the host tissue. Few commercially available skin substitutes allow limited vascularization. Moreover, the development of engineered skin is a time consuming process involving 2–3 weeks of cell culture before it is ready for grafting. Technical advances in cell and tissue culture protocols are required to overcome cell growth issues of skin substitutes. Currently, available skin substitutes mainly consist of fibroblasts and keratinocytes and therefore lack the ability to make differentiated structures, like hair and sweat glands. Therefore, there is a need to include additional cells types, such as endothelial cells in engineered skin. There is also a need to reduce the cost of current skin substitutes. The cost to cover 1% body surface area with Epicel™ is more than $13,000 [78,121]. In order to meet the massive demand for skin substitutes from hospitals for clinical applications, it is necessary to improve large-scale production.

9. Future Perspectives

Tissue engineered skin substitutes hold a promise for future tissue regeneration and wound healing therapeutics. There is still a need for improvement in vascularization of these substitutes to increase their life span and provide better integration with host tissues. One way of increasing vascularization is by using bioreactors to provide mechanical stimulation necessary to develop mature blood vessels [122]. An important step in developing reliable substitutes will be to standardize the production process and reduce manufacturing costs. Moreover, the standardization of storage and preservation is also important to extend their life spans. Further investigation is also required to assess the possibility of increased risk of future malignancies in such cells. One way to eradicate these issues will be to mimic more properties of in vivo skin. Although there is an urgent need to improve tissue engineered skin substitutes due to practical and therapeutic limitations, the field has come a long way in patient healing and does hold promise in the near future for skin and wound healing. Better and efficient products can be developed by a detailed understanding of the mechanism of the therapeutic action of bioengineered skin. There are several skin substitutes currently available, but skin substitutes constructed from a combination of stem cells and biomaterials remain a promising solution for the future.

Acknowledgments

Support for this review is provided by grants from the National Science Foundation NSF-CREST (HRD-1241701), NSF-HBCU-UP (HRD-1135863) and the US Department of Education—The Minority Science and Engineering Improvement Program (MSEIP) (P120A150008). The authors thank Golden Muse (www.golden-muse.com) for all illustrations in this review.

Author Contributions

Komal Vig, Atul Chaudhari, Shweta Tripathi, Saurabh Dixit and Rajnish Sahu contributed towards manuscript writing and figures; Shreekumar Pillai, Vida A. Dennis and Shree R. Singh contributed towards manuscript editing and critical revision.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Herndon, D.N.; Barrow, R.E.; Rutan, R.L.; Rutan, T.C.; Desai, M.H.; Abston, S. A comparison of conservative versus early excision. Therapies in severely burned patients. Ann. Surg. 1989, 209, 547–552. [Google Scholar] [CrossRef] [PubMed]
  2. Rheinwald, J.G. Human epidermal keratinocyte cell culture and xenograft systems: Applications in the detection of potential chemical carcinogens and the study of epidermal transformation. Prog. Clin. Biol. Res. 1989, 298, 113–125. [Google Scholar] [PubMed]
  3. Alonso, L.; Fuchs, E. Stem cells of the skin epithelium. Proc. Natl. Acad. Sci. USA 2003, 100, 11830–11835. [Google Scholar] [CrossRef] [PubMed]
  4. Clark, R.A.; Ghosh, K.; Tonnesen, M.G. Tissue engineering for cutaneous wounds. J. Investig. Dermatol. 2007, 127, 1018–1029. [Google Scholar] [CrossRef] [PubMed]
  5. De Mel, A.; Seifalian, A.M.; Birchall, M.A. Orchestrating cell/material interactions for tissue engineering of surgical implants. Macromol. Biosci. 2012, 12, 1010–1021. [Google Scholar] [CrossRef] [PubMed]
  6. Harvey, C. Wound healing. Orthop. Nurs. 2005, 24, 143–157. [Google Scholar] [CrossRef] [PubMed]
  7. Boyce, S.T.; Warden, G.D. Principles and practices for treatment of cutaneous wounds with cultured skin substitutes. Am. J. Surg. 2002, 183, 445–456. [Google Scholar] [CrossRef]
  8. Phillips, T.J. Current approaches to venous ulcers and compression. Dermatol. Surg. 2001, 27, 611–621. [Google Scholar] [PubMed]
  9. Braddock, M.; Campbell, C.J.; Zuder, D. Current therapies for wound healing: Electrical stimulation, biological therapeutics, and the potential for gene therapy. Int. J. Dermatol. 1999, 38, 808–817. [Google Scholar] [CrossRef] [PubMed]
  10. Wu, Y.; Chen, L.; Scott, P.G.; Tredget, E.E. Mesenchymal stem cells enhance wound healing through differentiation and angiogenesis. Stem Cells 2007, 25, 2648–2659. [Google Scholar] [CrossRef] [PubMed]
  11. Atiyeh, B.S.; Ioannovich, J.; Al-Amm, C.A.; El-Musa, K.A. Management of acute and chronic open wounds: The importance of moist environment in optimal wound healing. Curr. Pharm. Biotechnol. 2002, 3, 179–195. [Google Scholar] [CrossRef] [PubMed]
  12. Cole-King, A.; Harding, K.G. Psychological factors and delayed healing in chronic wounds. Psychosom. Med. 2001, 63, 216–220. [Google Scholar] [CrossRef] [PubMed]
  13. Walburn, J.; Vedhara, K.; Hankins, M.; Rixon, L.; Weinman, J. Psychological stress and wound healing in humans: A systematic review and meta-analysis. J. Psychosom. Res. 2009, 67, 253–271. [Google Scholar] [CrossRef] [PubMed]
  14. Rhett, J.M.; Ghatnekar, G.S.; Palatinus, J.A.; O’Quinn, M.; Yost, M.J.; Gourdie, R.G. Novel therapies for scar reduction and regenerative healing of skin wounds. Trends Biotechnol. 2008, 26, 173–180. [Google Scholar] [CrossRef] [PubMed]
  15. Janeway, C.A., Jr.; Walport, M.; Travers, P.; Shlomchik, M.J. Immunobiology: The Immune System in Health and Disease, 5th ed.; Garland Science: New York, NY, USA, 2001. [Google Scholar]
  16. Davis, J.S. Address of the president: The story of plastic surgery. Ann. Surg. 1941, 113, 641–656. [Google Scholar] [CrossRef] [PubMed]
  17. Akan, M.; Yildirim, S.; Misirlioglu, A.; Ulusoy, G.; Akoz, T.; Avci, G. An alternative method to minimize pain in the split-thickness skin graft donor site. Plast. Reconstr. Surg. 2003, 111, 2243–2249. [Google Scholar] [CrossRef] [PubMed]
  18. Bello, Y.M.; Falabella, A.F.; Eaglstein, W.H. Tissue-engineered skin. Current status in wound healing. Am. J. Clin. Dermatol. 2001, 2, 305–313. [Google Scholar] [CrossRef] [PubMed]
  19. Halim, A.S.; Khoo, T.L.; Mohd Yussof, S.J. Biologic and synthetic skin substitutes: An overview. Indian J. Plast. Surg. 2010, 43, 23–28. [Google Scholar] [CrossRef] [PubMed]
  20. Cardinal, M.; Eisenbud, D.E.; Armstrong, D.G.; Zelen, C.; Driver, V.; Attinger, C.; Phillips, T.; Harding, K. Serial surgical debridement: A retrospective study on clinical outcomes in chronic lower extremity wounds. Wound Repair Regen. 2009, 17, 306–311. [Google Scholar] [CrossRef] [PubMed]
  21. Rockwell, W.B.; Daane, S.; Zakhireh, M.; Carroll, K.L. Human skin allograft used to treat open wounds after club foot release. Ann. Plast. Surg. 2003, 51, 593–597. [Google Scholar] [CrossRef] [PubMed]
  22. Nathoo, R.; Howe, N.; Cohen, G. Skin substitutes: An overview of the key players in wound management. J. Clin. Aesthet. Dermatol. 2014, 7, 44–48. [Google Scholar] [PubMed]
  23. Shores, J.T.; Gabriel, A.; Gupta, S. Skin substitutes and alternatives: A review. Adv. Skin Wound Care 2007, 20, 493–508. [Google Scholar] [CrossRef] [PubMed]
  24. Bujang-Safawi, E.; Halim, A.S.; Khoo, T.L.; Dorai, A.A. Dried irradiated human amniotic membrane as a biological dressing for facial burns—A 7-year case series. Burns 2010, 36, 876–882. [Google Scholar] [CrossRef] [PubMed]
  25. Eskandarlou, M.; Azimi, M.; Rabiee, S.; Seif Rabiee, M.A. The healing effect of amniotic membrane in burn patients. World J. Plast. Surg. 2016, 5, 39–44. [Google Scholar] [PubMed]
  26. Fetterolf, D.E.; Snyder, R.J. Scientific and clinical support for the use of dehydrated amniotic membrane in wound management. Wounds Compend. Clin. Res. Pract. 2012, 24, 299–307. [Google Scholar]
  27. Thangapazham, R.L.; Darling, T.N.; Meyerle, J. Alteration of skin properties with autologous dermal fibroblasts. Int. J. Mol. Sci. 2014, 15, 8407–8427. [Google Scholar] [CrossRef] [PubMed]
  28. Li, A.; Pouliot, N.; Redvers, R.; Kaur, P. Extensive tissue-regenerative capacity of neonatal human keratinocyte stem cells and their progeny. J. Clin. Investig. 2004, 113, 390–400. [Google Scholar] [CrossRef] [PubMed]
  29. Fortunel, N.O.; Vaigot, P.; Cadio, E.; Martin, M.T. Functional investigations of keratinocyte stem cells and progenitors at a single-cell level using multiparallel clonal microcultures. Methods Mol. Biol. 2010, 585, 13–23. [Google Scholar] [PubMed]
  30. Dong, R.; Liu, X.; Liu, Y.; Deng, Z.; Nie, X.; Wang, X.; Jin, Y. Enrichment of epidermal stem cells by rapid adherence and analysis of the reciprocal interaction of epidermal stem cells with neighboring cells using an organotypic system. Cell Biol. Int. 2007, 31, 733–740. [Google Scholar] [CrossRef] [PubMed]
  31. King, A.; Balaji, S.; Keswani, S.G.; Crombleholme, T.M. The role of stem cells in wound angiogenesis. Adv. Wound Care 2014, 3, 614–625. [Google Scholar] [CrossRef] [PubMed]
  32. Dabiri, G.; Heiner, D.; Falanga, V. The emerging use of bone marrow-derived mesenchymal stem cells in the treatment of human chronic wounds. Expert Opin. Emerg. Drugs 2013, 18, 405–419. [Google Scholar] [CrossRef] [PubMed]
  33. Jackson, W.M.; Nesti, L.J.; Tuan, R.S. Concise review: Clinical translation of wound healing therapies based on mesenchymal stem cells. Stem Cells Transl. Med. 2012, 1, 44–50. [Google Scholar] [CrossRef] [PubMed]
  34. Nayak, S.; Dey, S.; Kundu, S.C. Skin equivalent tissue-engineered construct: Co-cultured fibroblasts/keratinocytes on 3d matrices of sericin hope cocoons. PLoS ONE 2013, 8, e74779. [Google Scholar] [CrossRef] [PubMed]
  35. Zuliani, T.; Saiagh, S.; Knol, A.C.; Esbelin, J.; Dreno, B. Fetal fibroblasts and keratinocytes with immunosuppressive properties for allogeneic cell-based wound therapy. PLoS ONE 2013, 8, e70408. [Google Scholar] [CrossRef] [PubMed]
  36. Dragunova, J.; Kabat, P.; Koller, J. Skin explant cultures as a source of keratinocytes for cultivation. Cell Tissue Bank. 2013, 14, 317–324. [Google Scholar] [CrossRef] [PubMed]
  37. Guerra, L.; Dellambra, E.; Panacchia, L.; Paionni, E. Tissue engineering for damaged surface and lining epithelia: Stem cells, current clinical applications, and available engineered tissues. Tissue Eng. Part B Rev. 2009, 15, 91–112. [Google Scholar] [CrossRef] [PubMed]
  38. Boehnke, K.; Mirancea, N.; Pavesio, A.; Fusenig, N.E.; Boukamp, P.; Stark, H.J. Effects of fibroblasts and microenvironment on epidermal regeneration and tissue function in long-term skin equivalents. Eur. J. Cell Biol. 2007, 86, 731–746. [Google Scholar] [CrossRef] [PubMed]
  39. Sun, T.; Jackson, S.; Haycock, J.W.; MacNeil, S. Culture of skin cells in 3D rather than 2D improves their ability to survive exposure to cytotoxic agents. J. Biotechnol. 2006, 122, 372–381. [Google Scholar] [CrossRef] [PubMed]
  40. Hill, D.S.; Robinson, N.D.; Caley, M.P.; Chen, M.; O’Toole, E.A.; Armstrong, J.L.; Przyborski, S.; Lovat, P.E. A novel fully humanized 3D skin equivalent to model early melanoma invasion. Mol. Cancer Ther. 2015, 14, 2665–2673. [Google Scholar] [CrossRef] [PubMed]
  41. Gallico, G.G.; O’Connor, N.E.; Compton, C.C.; Kehinde, O.; Green, H. Permanent coverage of large burn wounds with autologous cultured human epithelium. New Engl. J. Med. 1984, 311, 448–451. [Google Scholar] [CrossRef] [PubMed]
  42. O’Connor, N.E.; Mulliken, J.; Banks-Schlegel, S.; Green, H. Grafting of burns with cultured epithelium prepared from autologous epidermal cells. Lancet 1981, 317, 75–78. [Google Scholar] [CrossRef]
  43. Rheinwald, J.G.; Green, H. Serial cultivation of strains of human epidermal keratinocytes: The formation of keratinizing colonies from single cells. Cell 1975, 6, 331–343. [Google Scholar] [CrossRef]
  44. Rheinwald, J.G.; Green, H. Epidermal growth factor and the multiplication of cultured human epidermal keratinocytes. Nature 1977, 265, 421–424. [Google Scholar] [CrossRef] [PubMed]
  45. Leigh, I.M.; Watt, F.M. The culture of human epidermal keratinocytes. In Keratinocyte Handbook; Cambridge University Press: Cambridge, UK, 1994; pp. 43–51. [Google Scholar]
  46. Supp, D.M.; Boyce, S.T. Engineered skin substitutes: Practices and potentials. Clin. Dermatol. 2005, 23, 403–412. [Google Scholar] [CrossRef] [PubMed]
  47. Kroner, E.; Kaiser, J.S.; Fischer, S.C.; Arzt, E. Bioinspired polymeric surface patterns for medical applications. J. Appl. Biomater. Funct. Mater. 2012, 10, 287–292. [Google Scholar] [CrossRef] [PubMed]
  48. Ho, W.S. Skin substitutes: An overview. Ann. R. Coll. Surg. 2002, 6, 102–108. [Google Scholar] [CrossRef]
  49. Horch, R.E.; Kopp, J.; Kneser, U.; Beier, J.; Bach, A.D. Tissue engineering of cultured skin substitutes. J. Cell. Mol. Med. 2005, 9, 592–608. [Google Scholar] [CrossRef] [PubMed]
  50. Leigh, I.M.; Watt, F.M. Keratinocyte Methods; Cambridge University Press: Cambridge, UK, 1994. [Google Scholar]
  51. MacNeil, S. Progress and opportunities for tissue-engineered skin. Nature 2007, 445, 874–880. [Google Scholar] [CrossRef] [PubMed]
  52. Metcalfe, A.D.; Ferguson, M.W. Tissue engineering of replacement skin: The crossroads of biomaterials, wound healing, embryonic development, stem cells and regeneration. J. R. Soc. Interface 2007, 4, 413–437. [Google Scholar] [CrossRef] [PubMed]
  53. Boyce, S.T.; Kagan, R.J.; Meyer, N.A.; Yakuboff, K.P.; Warden, G.D. The 1999 clinical research award. Cultured skin substitutes combined with integra artificial skin to replace native skin autograft and allograft for the closure of excised full-thickness burns. J. Burn Care Rehabil. 1999, 20, 453–461. [Google Scholar] [CrossRef] [PubMed]
  54. Passaretti, D.; Billmire, D.; Kagan, R.; Corcoran, J.; Boyce, S. Autologous cultured skin substitutes conserve donor autograft in elective treatment of congenital giant melanocytic nevus. Plast. Reconstr. Surg. 2004, 114, 1523–1528. [Google Scholar] [CrossRef] [PubMed]
  55. Shevchenko, R.V.; James, S.L.; James, S.E. A review of tissue-engineered skin bioconstructs available for skin reconstruction. J. R. Soc. Interface 2010, 7, 229–258. [Google Scholar] [CrossRef] [PubMed]
  56. Atiyeh, B.S.; Costagliola, M. Cultured epithelial autograft (CEA) in burn treatment: Three decades later. Burns 2007, 33, 405–413. [Google Scholar] [CrossRef] [PubMed]
  57. Patel, M.; Fisher, J.P. Biomaterial scaffolds in pediatric tissue engineering. Pediatr. Res. 2008, 63, 497–501. [Google Scholar] [CrossRef] [PubMed]
  58. Shakespeare, P.; Shakespeare, V. Survey: Use of skin substitute materials in UK burn treatment centres. Burns 2002, 28, 295–297. [Google Scholar] [CrossRef]
  59. Shakespeare, P.G. The role of skin substitutes in the treatment of burn injuries. Clin. Dermatol. 2005, 23, 413–418. [Google Scholar] [CrossRef] [PubMed]
  60. Melkun, E.T.; Few, J.W. The use of biosynthetic skin substitute (Biobrane) for axillary reconstruction after surgical excision for hidradenitis suppurativa. Plast. Reconstr. Surg. 2005, 115, 1385–1388. [Google Scholar] [CrossRef] [PubMed]
  61. Curran, M.P.; Plosker, G.L. Bilayered bioengineered skin substitute (Apligraf): A review of its use in the treatment of venous leg ulcers and diabetic foot ulcers. BioDrugs 2002, 16, 439–455. [Google Scholar] [CrossRef] [PubMed]
  62. Price, R.D.; Myers, S.; Leigh, I.M.; Navsaria, H.A. The role of hyaluronic acid in wound healing: Assessment of clinical evidence. Am. J. Clin. Dermatol. 2005, 6, 393–402. [Google Scholar] [CrossRef] [PubMed]
  63. Hellman, K.B. Engineered tissues: The regulatory path from concept to market. Adv. Exp. Med. Biol. 2006, 585, 363–376. [Google Scholar] [PubMed]
  64. Alrubaiy, L.; Al-Rubaiy, K.K. Skin substitutes: A brief review of types and clinical applications. Oman Méd. J. 2009, 24, 4–6. [Google Scholar] [CrossRef] [PubMed]
  65. Gordley, K.; Cole, P.; Hicks, J.; Hollier, L. A comparative, long term assessment of soft tissue substitutes: Alloderm, enduragen, and dermamatrix. JPRAS 2009, 62, 849–850. [Google Scholar] [CrossRef] [PubMed]
  66. Hodde, J.P.; Ernst, D.M.; Hiles, M.C. An investigation of the long-term bioactivity of endogenous growth factor in oasis wound matrix. J. Wound Care 2005, 14, 23–25. [Google Scholar] [CrossRef] [PubMed]
  67. Tausche, A.K.; Skaria, M.; Bohlen, L.; Liebold, K.; Hafner, J.; Friedlein, H.; Meurer, M.; Goedkoop, R.J.; Wollina, U.; Salomon, D.; et al. An autologous epidermal equivalent tissue-engineered from follicular outer root sheath keratinocytes is as effective as split-thickness skin autograft in recalcitrant vascular leg ulcers. Wound Repair Regen. 2003, 11, 248–252. [Google Scholar] [CrossRef] [PubMed]
  68. Haddow, D.B.; Steele, D.A.; Short, R.D.; Dawson, R.A.; Macneil, S. Plasma-polymerized surfaces for culture of human keratinocytes and transfer of cells to an in vitro wound-bed model. J. Biomed. Mater. Res. Part A 2003, 64, 80–87. [Google Scholar] [CrossRef] [PubMed]
  69. Hüsing, B.; Bührlen, B.; Gaisser, S. Human tissue engineered products: Today’s markets and future prospects. Fraunhofer Inst. Syst. Innov. Res. 2003, 1, 54. [Google Scholar]
  70. Goedkoop, R.; Juliet, R.; You, P.H.; Daroczy, J.; de Roos, K.P.; Lijnen, R.; Rolland, E.; Hunziker, T. Wound stimulation by growth-arrested human keratinocytes and fibroblasts: Hp802-247, a new-generation allogeneic tissue engineering product. Dermatology 2010, 220, 114–120. [Google Scholar] [CrossRef] [PubMed]
  71. Kirsner, R.S.; Marston, W.A.; Snyder, R.J.; Lee, T.D.; Cargill, D.I.; Slade, H.B. Spray-applied cell therapy with human allogeneic fibroblasts and keratinocytes for the treatment of chronic venous leg ulcers: A phase 2, multicentre, double-blind, randomised, placebo-controlled trial. Lancet 2012, 380, 977–985. [Google Scholar] [CrossRef]
  72. Magnusson, M.; Papini, R.P.; Rea, S.M.; Reed, C.C.; Wood, F.M. Cultured autologous keratinocytes in suspension accelerate epithelial maturation in an in vivo wound model as measured by surface electrical capacitance. Plast. Reconstr. Surg. 2007, 119, 495–499. [Google Scholar] [CrossRef] [PubMed]
  73. Carsin, H.; Ainaud, P.; Le Bever, H.; Rives, J.; Lakhel, A.; Stephanazzi, J.; Lambert, F.; Perrot, J. Cultured epithelial autografts in extensive burn coverage of severely traumatized patients: A five year single-center experience with 30 patients. Burns 2000, 26, 379–387. [Google Scholar] [CrossRef]
  74. Caravaggi, C.; de Giglio, R.; Pritelli, C.; Sommaria, M.; Dalla Noce, S.; Faglia, E.; Mantero, M.; Clerici, G.; Fratino, P.; Dalla Paola, L.; et al. Hyaff 11-based autologous dermal and epidermal grafts in the treatment of noninfected diabetic plantar and dorsal foot ulcers: A prospective, multicenter, controlled, randomized clinical trial. Diabetes Care 2003, 26, 2853–2859. [Google Scholar] [CrossRef] [PubMed]
  75. Dietz, J.; Lundgren, P.; Veeramani, A.; O’Rourke, C.; Bernard, S.; Djohan, R.; Larson, J.; Isakov, R.; Yetman, R. Autologous inferior dermal sling (Autoderm) with concomitant skin-envelope reduction mastectomy: An excellent surgical choice for women with macromastia and clinically significant ptosis. Ann. Surg. Oncol. 2012, 19, 3282–3288. [Google Scholar] [CrossRef] [PubMed]
  76. Harding, K.G.; Krieg, T.; Eming, S.A.; Flour, M.L.; Jawien, A.; Cencora, A.; Kaszuba, A.; Noszcyk, W.; Willems, P.; de Deene, A.; et al. Efficacy and safety of the freeze-dried cultured human keratinocyte lysate, lyphoderm 0.9%, in the treatment of hard-to-heal venous leg ulcers. Wound Repair Regen. 2005, 13, 138–147. [Google Scholar] [CrossRef] [PubMed]
  77. Paquet, P.; Quatresooz, P.; Braham, C.; Pierard, G.E. Tapping into the influence of keratinocyte allografts and biocenosis on healing of chronic leg ulcers: Split-ulcer controlled pilot study. Dermatol. Surg. 2005, 31, 431–435. [Google Scholar] [CrossRef] [PubMed]
  78. Varkey, M.; Ding, J.; Tredget, E.E. Advances in skin substitutes-potential of tissue engineered skin for facilitating anti-fibrotic healing. J. Funct. Biomater. 2015, 6, 547–563. [Google Scholar] [CrossRef] [PubMed]
  79. Limova, M. Active wound coverings: Bioengineered skin and dermal substitutes. Surg. Clin. N. Am. 2010, 90, 1237–1255. [Google Scholar] [CrossRef] [PubMed]
  80. Uccioli, L. A clinical investigation on the characteristics and outcomes of treating chronic lower extremity wounds using the tissuetech autograft system. Int. J. Low. Extremity Wounds 2003, 2, 140–151. [Google Scholar] [CrossRef] [PubMed]
  81. Noordenbos, J.; Dore, C.; Hansbrough, J.F. Safety and efficacy of transcyte for the treatment of partial-thickness burns. J. Burn Care Rehabil. 1999, 20, 275–281. [Google Scholar] [CrossRef] [PubMed]
  82. Groeber, F.; Holeiter, M.; Hampel, M.; Hinderer, S.; Schenke-Layland, K. Skin tissue engineering—In vivo and in vitro applications. Adv. Drug Deliv. Rev. 2011, 63, 352–366. [Google Scholar] [CrossRef] [PubMed]
  83. Ng, K.W.; Hutmacher, D.W. Reduced contraction of skin equivalent engineered using cell sheets cultured in 3D matrices. Biomaterials 2006, 27, 4591–4598. [Google Scholar] [CrossRef] [PubMed]
  84. Myers, S.R.; Partha, V.N.; Soranzo, C.; Price, R.D.; Navsaria, H.A. Hyalomatrix: A temporary epidermal barrier, hyaluronan delivery, and neodermis induction system for keratinocyte stem cell therapy. Tissue Eng. 2007, 13, 2733–2741. [Google Scholar] [CrossRef] [PubMed]
  85. Cullen, B. The role of oxidized regenerated cellulose/collagen in chronic wound repair. Part 2. Ostomy Wound Manag. 2002, 48, 8–13. [Google Scholar]
  86. Stark, H.J.; Boehnke, K.; Mirancea, N.; Willhauck, M.J.; Pavesio, A.; Fusenig, N.E.; Boukamp, P. Epidermal homeostasis in long-term scaffold-enforced skin equivalents. J. Investig. Dermatol. Symp. Proc. 2006, 11, 93–105. [Google Scholar] [CrossRef] [PubMed]
  87. Ackermann, K.; Borgia, S.L.; Korting, H.C.; Mewes, K.R.; Schafer-Korting, M. The phenion full-thickness skin model for percutaneous absorption testing. Skin Pharmacol. Physiol. 2010, 23, 105–112. [Google Scholar] [CrossRef] [PubMed]
  88. Still, J.; Glat, P.; Silverstein, P.; Griswold, J.; Mozingo, D. The use of a collagen sponge/living cell composite material to treat donor sites in burn patients. Burns 2003, 29, 837–841. [Google Scholar] [CrossRef]
  89. Lindberg, K.; Badylak, S.F. Porcine small intestinal submucosa (SIS): A bioscaffold supporting in vitro primary human epidermal cell differentiation and synthesis of basement membrane proteins. Burns 2001, 27, 254–266. [Google Scholar] [CrossRef]
  90. Rockwood, D.N.; Woodhouse, K.A.; Fromstein, J.D.; Chase, D.B.; Rabolt, J.F. Characterization of biodegradable polyurethane microfibers for tissue engineering. J. Biomater. Sci. Polym. 2007, 18, 743–758. [Google Scholar] [CrossRef] [PubMed]
  91. Van Dorp, A.G.; Verhoeven, M.C.; Koerten, H.K.; van Blitterswijk, C.A.; Ponec, M. Bilayered biodegradable poly (ethylene glycol)/poly (butylene terephthalate) copolymer (polyactive) as substrate for human fibroblasts and keratinocytes. J. Biomed. Mater. Res. 1999, 47, 292–300. [Google Scholar] [CrossRef]
  92. Dodson, B.P.; Levine, A.D. Challenges in the translation and commercialization of cell therapies. BMC Biotechnol. 2015, 15, 70. [Google Scholar] [CrossRef] [PubMed]
  93. Ferreira, M.C.; Paggiaro, A.O.; Isaac, C.; Teixeira Neto, N.; dos Santos, G.B. Skin substitutes: Current concepts and a new classification system. Rev. Bras. Cir. Plást. 2011, 26, 696–702. [Google Scholar] [CrossRef]
  94. Centanni, J.M.; Straseski, J.A.; Wicks, A.; Hank, J.A.; Rasmussen, C.A.; Lokuta, M.A.; Schurr, M.J.; Foster, K.N.; Faucher, L.D.; Caruso, D.M.; et al. Stratagraft skin substitute is well-tolerated and is not acutely immunogenic in patients with traumatic wounds: Results from a prospective, randomized, controlled dose escalation trial. Ann. Surg. 2011, 253, 672–683. [Google Scholar] [CrossRef] [PubMed]
  95. Schurr, M.J.; Foster, K.N.; Centanni, J.M.; Comer, A.R.; Wicks, A.; Gibson, A.L.; Thomas-Virnig, C.L.; Schlosser, S.J.; Faucher, L.D.; Lokuta, M.A.; et al. Phase I/II clinical evaluation of stratagraft: A consistent, pathogen-free human skin substitute. J. Trauma 2009, 66, 866–873. [Google Scholar] [CrossRef] [PubMed]
  96. Supp, D.M.; Karpinski, A.C.; Boyce, S.T. Expression of human β-defensins HBD-1, HBD-2, and HBD-3 in cultured keratinocytes and skin substitutes. Burns 2004, 30, 643–648. [Google Scholar] [CrossRef] [PubMed]
  97. Cheah, A.K.W.; Chong, S.J.; Tan, B.K. Early experience with biobrane™ in singapore in the management of partial thickness burns. Proc. Singap. Healthc. 2014, 23, 196–200. [Google Scholar] [CrossRef]
  98. Chua, A.W.; Khoo, Y.C.; Tan, B.K.; Tan, K.C.; Foo, C.L.; Chong, S.J. Skin tissue engineering advances in severe burns: Review and therapeutic applications. Burns Trauma 2016, 4, 3. [Google Scholar] [CrossRef] [PubMed]
  99. Greenwood, J.E.; Clausen, J.; Kavanagh, S. Experience with biobrane: Uses and caveats for success. Eplasty 2009, 9, e25. [Google Scholar] [PubMed]
  100. Tan, H.; Wasiak, J.; Paul, E.; Cleland, H. Effective use of biobrane as a temporary wound dressing prior to definitive split-skin graft in the treatment of severe burn: A retrospective analysis. Burns 2015, 41, 969–976. [Google Scholar] [CrossRef] [PubMed]
  101. Woodroof, E.A. The search for an ideal temporary skin substitute: Awbat. Eplasty 2009, 9, e10. [Google Scholar] [PubMed]
  102. Conconi, M.T.; de Coppi, P.; di Liddo, R.; Vigolo, S.; Zanon, G.F.; Parnigotto, P.P.; Nussdorfer, G.G. Tracheal matrices, obtained by a detergent-enzymatic method, support in vitro the adhesion of chondrocytes and tracheal epithelial cells. Transplant Int. 2005, 18, 727–734. [Google Scholar] [CrossRef] [PubMed]
  103. Shahrokhi, S.; Arno, A.; Jeschke, M.G. The use of dermal substitutes in burn surgery: Acute phase. Wound Repair Regen. 2014, 22, 14–22. [Google Scholar] [CrossRef] [PubMed]
  104. Dickinson, L.E.; Gerecht, S. Engineered biopolymeric scaffolds for chronic wound healing. Front. Physiol. 2016, 7, 341. [Google Scholar] [CrossRef] [PubMed]
  105. Lev-Tov, H.; Li, C.S.; Dahle, S.; Isseroff, R.R. Cellular versus acellular matrix devices in treatment of diabetic foot ulcers: Study protocol for a comparative efficacy randomized controlled trial. Trials 2013, 14, 8. [Google Scholar] [CrossRef] [PubMed]
  106. Raguse, J.D.; Gath, H.J. The buccal fad pad lined with a metabolic active dermal replacement (dermagraft) for treatment of defects of the buccal plane. Br. J. Plast. Surg. 2004, 57, 764–768. [Google Scholar] [CrossRef] [PubMed]
  107. Armstrong, D.G.; Lepow, B.D.; Downey, M.; Yurgelon, J.; Klassen, L. Bioengineered tissues in wound healing a progress report. Expert Rev. Dermatol. 2011, 6, 255–262. [Google Scholar]
  108. Kim, P.J.; Heilala, M.; Steinberg, J.S.; Weinraub, G.M. Bioengineered alternative tissues and hyperbaric oxygen in lower extremity wound healing. Clin. Podiatr. Med. Surg. 2007, 24, 529–546. [Google Scholar] [CrossRef] [PubMed]
  109. Ryssel, H.; Gazyakan, E.; Germann, G.; Ohlbauer, M. The use of matriderm in early excision and simultaneous autologous skin grafting in burns—A pilot study. Burns 2008, 34, 93–97. [Google Scholar] [CrossRef] [PubMed]
  110. Kolokythas, P.; Aust, M.C.; Vogt, P.M.; Paulsen, F. Dermal subsitute with the collagen-elastin matrix matriderm in burn injuries: A comprehensive review. Handchir. Mikrochir. Plast. Chir. 2008, 40, 367–371. [Google Scholar] [CrossRef] [PubMed]
  111. Van Zuijlen, P.P.; van Trier, A.J.; Vloemans, J.F.; Groenevelt, F.; Kreis, R.W.; Middelkoop, E. Graft survival and effectiveness of dermal substitution in burns and reconstructive surgery in a one-stage grafting model. Plast. Reconstr. Surg. 2000, 106, 615–623. [Google Scholar] [CrossRef] [PubMed]
  112. Greenberg, J.E.; Falabella, A.F.; Bello, Y.M.; Schachner, L.A. Tissue-engineered skin in the healing of wound stumps from limb amputations secondary to purpura fulminans. Pediatr. Dermatol. 2003, 20, 169–172. [Google Scholar] [CrossRef] [PubMed]
  113. Akkouch, A.; Shi, G.; Zhang, Z.; Rouabhia, M. Bioactivating electrically conducting polypyrrole with fibronectin and bovine serum albumin. J. Biomed. Mater. Res. Part A 2010, 92, 221–231. [Google Scholar] [CrossRef] [PubMed]
  114. Cui, X.; Hetke, J.F.; Wiler, J.A.; Anderson, D.J.; Martin, D.C. Electrochemical deposition and characterization of conducting polymer polypyrrole/PSS on multichannel neural probes. Sens. Actuators A Phys. 2001, 93, 8–18. [Google Scholar] [CrossRef]
  115. Li, Y.; Neoh, K.G.; Kang, E.T. Plasma protein adsorption and thrombus formation on surface functionalized polypyrrole with and without electrical stimulation. J. Colloid Interface Sci. 2004, 275, 488–495. [Google Scholar] [CrossRef] [PubMed]
  116. Austin, R.E.; Merchant, N.; Shahrokhi, S.; Jeschke, M.G. A comparison of biobrane and cadaveric allograft for temporizing the acute burn wound: Cost and procedural time. Burns 2015, 41, 749–753. [Google Scholar] [CrossRef] [PubMed]
  117. Cooper, M.L.; Andree, C.; Hansbrough, J.F.; Zapata-Sirvent, R.L.; Spielvogel, R.L. Direct comparison of a cultured composite skin substitute containing human keratinocytes and fibroblasts to an epidermal sheet graft containing human keratinocytes on athymic mice. J. Investig. Dermatol. 1993, 101, 811–819. [Google Scholar] [CrossRef] [PubMed]
  118. Farroha, A.; Frew, Q.; El-Muttardi, N.; Philp, B.; Dziewulski, P. The use of biobrane® to dress split-thickness skin graft in paediatric burns. Ann. Burns Fire Disasters 2013, 26, 94–97. [Google Scholar] [PubMed]
  119. Pandya, A.N.; Woodward, B.; Parkhouse, N. The use of cultured autologous keratinocytes with integra in the resurfacing of acute burns. Plast. Reconstr. Sur. 1998, 102, 825–828. [Google Scholar] [CrossRef]
  120. Pham, C.; Greenwood, J.; Cleland, H.; Woodruff, P.; Maddern, G. Bioengineered skin substitutes for the management of burns: A systematic review. Burns 2007, 33, 946–957. [Google Scholar] [CrossRef] [PubMed]
  121. Rue, L.W., 3rd; Cioffi, W.G.; McManus, W.F.; Pruitt, B.A. Wound closure and outcome in extensively burned patients treated with cultured autologous keratinocytes. J. Trauma 1993, 34, 662–667. [Google Scholar] [CrossRef] [PubMed]
  122. Lovett, M.; Lee, K.; Edwards, A.; Kaplan, D.L. Vascularization strategies for tissue engineering. Tissue Eng. Part B Rev. 2009, 15, 353–370. [Google Scholar] [CrossRef] [PubMed]
Ijms 18 00789 g001 550
Figure 1. Normal skin structure.
Figure 1. Normal skin structure.
Ijms 18 00789 g001
Ijms 18 00789 g002 550
Figure 2. Tissue engineered skin substitute preparation. Bold lines indicate cell type for tissue engineered substitute and dotted lines indicate cell source.
Figure 2. Tissue engineered skin substitute preparation. Bold lines indicate cell type for tissue engineered substitute and dotted lines indicate cell source.
Ijms 18 00789 g002
Ijms 18 00789 g003 550
Figure 3. Tissue engineered skin substitutes. (a) Acellular: i. Karoderm ii. Biobrane iii. Integra (b) Epidermal Autologous: i. Cell Spray ii. Epicel iii. Laserskin (c) Dermal Autologous: i. Hyalograft 3D (d) Dermal Allogenic: i. TransCyte ii. Dermagraft (e) Dermal Xenogenic: i. Permacol (f) Epidermal/Dermal (Composite) Autologous i. Tissue tech Autograft system (g) Epidermal/Dermal (Composite) Allograft i. Apligraf.
Figure 3. Tissue engineered skin substitutes. (a) Acellular: i. Karoderm ii. Biobrane iii. Integra (b) Epidermal Autologous: i. Cell Spray ii. Epicel iii. Laserskin (c) Dermal Autologous: i. Hyalograft 3D (d) Dermal Allogenic: i. TransCyte ii. Dermagraft (e) Dermal Xenogenic: i. Permacol (f) Epidermal/Dermal (Composite) Autologous i. Tissue tech Autograft system (g) Epidermal/Dermal (Composite) Allograft i. Apligraf.
Ijms 18 00789 g003
Table
Table 1. Commercially available skin substitutes.
Table 1. Commercially available skin substitutes.
Substitute TypeProductCompanyComponentsReferences
AcellularAlloderm®LifeCell Inc., Branchburg, NJ, USAHuman acellular lyophilized dermis[18,22,46,49,65]
SureDermHANS BIOMED Corporation, Daejeon, KoreaHuman acellular lyophilized dermis-
OASIS Wound MatrixCook Biotech Inc., West Lafayette, IN, USAPorcine acellular lyophilized small intestine submucosa[66]
Biobrane®Mylan Bertek Pharmaceuticals, USAUltrathin silicone as epidermal analog film and 3D nylon filament as dermal analog with type I collagen peptides[46,49,55]
Integra® DRT (dermal regeneration template)Integra® LifeSciences Corp., USADermal analog—bovine collagen and chondroitin-6-sulfate GAG; epidermal analog—silicone polymer polysiloxane[18,46,49,55]
Epidermal
AutologousEpiDexModex Therapeutiques, Lausanne, SwitzerlandCultured keratinocytes from outer root sheath of scalp hair follicles (confluent cell sheet)[67]
EPIBASELaboratoires Genevrier, Antibes, FranceCultured keratinocytes (confluent cell sheet)-
MySkinCellTran Ltd., UKCultured keratinocytes (subconfluent cell sheet) silicone support layer with a specially formulated surface coating[68]
Bioseed-SBioTissue Technologies GmbH, GermanyCultured keratinocytes (subconfluent cell suspension) fibrin sealant[69]
CellSprayClinical Cell Culture (C3), AustraliaNon-/cultured keratinocytes (subconfluent cell suspension)[70,71,72]
Epicel®Genzyme Biosurgery, USASheets of autologous keratinocytes attached to petrolatum gauze support[73]
Laserskin® or VivodermFidia Advanced Biopolymers Srl, ItalyAutologous keratinocytes and fibroblasts, grown on microperforated hyaluronic acid membranes[74]
Autoderm (Autologous Inferior Dermal Sling)XCELLentis NV, BelgiumCultured keratinocytes[75]
TransDermXCELLentis NV, BelgiumCultured keratinocytes[75]
LyphodermXCELLentis NV, BelgiumLyophilized neonatal keratinocytes [76]
CryocealXCELLentis NV, BelgiumCryopreserved keratinocytes[77]
Dermal
AutologousdenovoDerm™EUROSKINGRAFT, SwitzerlandAutologous dermal substitute[78]
Pelnac Standard/FortifiedGunze Ltd., JapanPorcine tendon derived atelocollagen type I, sponge layer with silicone film -
Hyalomatrix PAFidia Advanced Biopolymers, ItalyHYAFF (an ester of hyaluronic acid) layered on silicone membrane-
Hyalograft 3DFidia Advanced Biopolymers, ItalyCultured fibroblasts hyaluronic acid membrane (HAM)[79,80]
AllogenicDermagraft®Advanced BioHealing, Inc., USABioabsorbable polygalactin mesh matrix seeded with human neonatal fibroblasts and cryopreserved[78]
TransCyte®Advanced BioHealing, Inc., USACollagen-coated nylon mesh seeded with allogenic neonatal human foreskin fibroblasts [81]
TerudermisOlympus Terumo Biomaterial Corp., JapanSilicone, bovine lyophilized crosslinked collagen sponge made of heat-denatured collagen[82]
Cyzact (ICX-PRO)Intercytex, St John’s Innovation Center, UKCultured allogeneic human dermal fibroblasts embedded in a human fibrin gel matrix -
ICX-SKN skin graft replacementIntercytex, St John’s Innovation Center, UKCultured dermal fibroblasts natural human collagen matrix-
Polycaprolactone collagen nanofibrous membraneNational University of Singapore, SingaporeCultured dermal fibroblasts polycaprolactone-blended collagen electrospun nanofibrous membrane[83]
Tegaderm-nanofibre constructNational University of Singapore, SingaporeCultured dermal fibroblasts poly(e -caprolactone)/gelatin nanofibrous scaffold electrospun on polyurethane dressing-
Collagen–glycosaminoglycan–chitosan dermal matrix seeded with fibroblastsINSERM, FranceCultured dermal fibroblasts bovine collagen I/chondroitin-4/6-sulfate/chitosan lyophilized dermal matrix[46,49,55]
Human hair keratincollagen spongeSouthern Medical University, ChinaCryomilled porcine acellular diisocyanite cross-linked dermis-
Hyaluronan-FNfds hydrogel matrixSUNY at Stony Brook, USAHyaluronan coupled with fibronectin functional domains[84]
Composite nano-titanium oxide–chitosan artificial skin (NTCAS)Cardinal Tien College of Healthcare and Management, TaiwanComposite nano-titanium oxide–chitosan with gelatin and hyaluronic acid-
XenogeneicPermacol Surgical ImplantTissue Science Laboratories plc, UKPorcine acellular diisocyanite crosslinked dermis[79,85]
MatridermDr Suwelack Skin and HealthCare AG, GermanyBovine non-cross-linked lyophilized dermis, coated with a-elastin hydrolysate[79,85]
EZ DermTMBrennen Medical Inc., USAPorcine aldehyde cross-linked reconstituted dermal collagen[18]
Bovine collagen cross-linked with microbial transglutaminaseNational University of Ireland, IrelandFreeze-dried bovine collagen scaffold cross-linked with microbial transglutaminase[86,87,88]
CollatampSYNTACOLL AG, SwitzerlandMultilayer bovine collagen matrix-
SyntheticHybrid nanofibrous PLGA/chitosan membraneTianjin University, ChinaPLGA/chitosan hybrid electrospun nanofibrous membrane[83,89]
Biodegradable polyurethane microfibersUniversity of Delaware, USABiodegradable polyurethane microfibres[90]
Epidermal/Dermal (Composite)
AutologousPermaderm™ (Cincinnati Shriners Skin Substitute)Regeninic Inc.USAAutologous fibroblasts and keratinocytes in culture with bovine collagen and GAG substrates[78]
Tiscover™ (A-Skin)Advanced Tissue Medicinal Product, NetherlandsAutologous full thickness cultured skin[78]
denovoSkin™EUROSKINGRAFT, Univ. of Zurich, SwitzerlandAutologous full thickness substitute consisting of dermal and epidermal layers[78]
PolyActiveHC Implants BV, NetherlandsCultured keratinocytes and fibroblasts polyethylene oxide terephthalate (PEO)/polybutylene terephthalate (PBT)[91]
TissueTech Autograft System (Laserskin and Hyalograft 3D)Fidia Advanced Biopolymers, ItalyCultured keratinocytes and fibroblasts microperforated hyaluronic acid membrane (HAM)[74,79]
AllogenicApligraf®Organogenesis Inc., USABovine collagen matrix seeded with neonatal foreskin fibroblasts and keratinocytes[19,63,92,93]
OrCel®Ortec International Inc., USAType I collagen matrix seeded with neonatal foreskin fibroblasts and keratinocytes[86,87,88]
Karoskin (Karocells)Karocell Tissue Engineering AB, SwedenNative human cadaver skin with dermal and epidermal cells[55]
CeladermTMCeladon Science LLC, USASheets of cells derived from neonatal (allogenic) foreskin[19,63,92,93]
StrataGraft™Stratatech Corporation, USAFull thickness skin substitute with dermal and fully differentiated epidermal layers[79,94,95,96]
AcuDressDFB Pharmaceuticals, Inc., USACultured keratinocytes fibrin substrate-
AlloxDFB Pharmaceuticals, Inc., USASprayed suspension of allogeneic keratinocytes and fibroblasts in fibrin substrate-
XenogeneicOasis®Healthpoint Biotherapeutics, USAIntact matrix from porcine small-intestine submucosa and intended for wound closure stimulation in acute, chronic and burns wounds[79,85]

Share and Cite

MDPI and ACS Style

Vig, K.; Chaudhari, A.; Tripathi, S.; Dixit, S.; Sahu, R.; Pillai, S.; Dennis, V.A.; Singh, S.R. Advances in Skin Regeneration Using Tissue Engineering. Int. J. Mol. Sci. 2017, 18, 789. https://doi.org/10.3390/ijms18040789

AMA Style

Vig K, Chaudhari A, Tripathi S, Dixit S, Sahu R, Pillai S, Dennis VA, Singh SR. Advances in Skin Regeneration Using Tissue Engineering. International Journal of Molecular Sciences. 2017; 18(4):789. https://doi.org/10.3390/ijms18040789

Chicago/Turabian Style

Vig, Komal, Atul Chaudhari, Shweta Tripathi, Saurabh Dixit, Rajnish Sahu, Shreekumar Pillai, Vida A. Dennis, and Shree R. Singh. 2017. "Advances in Skin Regeneration Using Tissue Engineering" International Journal of Molecular Sciences 18, no. 4: 789. https://doi.org/10.3390/ijms18040789

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop