|Year : 2017 | Volume
| Issue : 1 | Page : 1-8
Regenerative medicine: Clinical applications and future perspectives
Federica Colombo1, Gianluca Sampogna1, Giovanni Cocozza1, Salman Yousuf Guraya2, Antonello Forgione1
1 Advanced International Mini-invasive Surgery – AIMS Academy, Milan, Italy
2 Department of Surgery and Consultant Colorectal Surgeon, College of Medicine, Taibah University, Almadinah Almunawwarah, KSA
|Date of Web Publication||8-Feb-2018|
Advanced International Mini-invasive Surgery – AIMS Academy, Milan
Source of Support: None, Conflict of Interest: None
After many years of basic research, regenerative medicine (RM) is now beginning to represent a valuable tool to cure several clinical conditions in both acute injuries and chronic diseases. The aim of this study is to update readers on current clinical applications of some selected organs and pathologies which may benefit from RM. An extensive literature research was performed using PubMed, Google and specialized journals. RM has achieved great successes, but there are still several challenges to tackle before it could be used on a daily basis in clinical practice. The crucial point of this revolution is represented by the appropriate and valid translation from bench to bedside.
Keywords: Regenerative medicine, Tissue engineering, Artificial organs, Cell therapy, Translational medicine.
|How to cite this article:|
Colombo F, Sampogna G, Cocozza G, Guraya SY, Forgione A. Regenerative medicine: Clinical applications and future perspectives. J Microsc Ultrastruct 2017;5:1-8
|How to cite this URL:|
Colombo F, Sampogna G, Cocozza G, Guraya SY, Forgione A. Regenerative medicine: Clinical applications and future perspectives. J Microsc Ultrastruct [serial online] 2017 [cited 2019 Jun 17];5:1-8. Available from: http://www.jmau.org/text.asp?2017/5/1/1/224939
| 1. Introduction|| |
Regenerative medicine (RM), from tissue engineering (TE) to cell therapy, offers valuable treatment options, which are rarely considered in daily clinical settings  Doctors, surgeons, clinicians and, in general, health-care policies are not prone to substitute conventional approaches with innovative therapies without extended and thorough experiments. A major concern that limits the spreading of RM is related to different challenges to solve definitively, e.g. live tissue handling and manufacturing .
In this article, the authors show how RM principles may be applied, presenting some examples of artificial tissues and organs, which could be considered as a valid purpose in daily clinical settings ,. At present, RM is not the gold standard treatment for all the most common diseases. On the one hand, clinicians are not well informed about the current applications; on the other hand, there are not many studies confirming safety, efficiency and effectiveness.
Therefore, we provide a brief reflection on the current pre-clinical and clinical applications with their advantages on traditional approaches and the issues that still need to be solved before a massive spread. Further research is mandatory to offer the definitive cure for both acute injuries and chronic diseases, but, first of all, clinicians should be informed of these possibilities and, later, form multidisci-plinary team to adopt and deliver these new treatments.
| 2. Materials and methods|| |
An exhaustive research of the latest clinical applications of RM was conducted using appropriate index terms (i.e. name of the organ AND tissue engineering or regenerative medicine AND clinical applications). These words were typed in scientific databases and search engine, like PubMed, Scopus, ScienceDirect and Google Scholar, to obtain articles from specialized journals (e.g. The Lancet, The Journal of Urology, Future Medicine Journals or the open access scientific journal PLoS ONE). We selected original articles written in English and published within the last two decades. Actually, most papers dated back to last five years; the older ones are related to key steps in the delivering of latest solutions.
Images were taken from PLoS ONE, as they could be freely used and inserted into the present review .
| 3. Specific organs and tissues|| |
Scientists are developing all kinds of tissues and organs (from bladder to heart, from nerve to ovary etc); unfortunately, just some of them have been already implanted successfully in humans, while others are still in pre-clinical phase, or have been developed recently . We selected and reported below some artificial tissues and organs, which have the potential to be implanted into humans on routine clinical settings.
Urinary bladder is a hollow organ, made up of two functional layers: an inner epithelium and an outer smooth muscle layer. Therefore, its regeneration requires both these layers in order to be successful. The gold standard treatment for patients with pathologic bladders, which are not responsive to any drugs, is to substitute or augment the original bladder with bowel segments. However, the gastrointestinal (GI) tissue is not adequate to stay in contact with urine, as it is supposed to adsorb solutes, which are normally accumulated and excreted. Therefore, it leads to several complications: mucous production, urolithiasis, infection, perforation, metabolic disturbances and even cancer . These issues have generated sufficient debate and novel research strategies are demanded to avoid the unwanted effects mentioned above. However, the storage and voiding functions associated to a good compliance and capacity of this organ are challenging to reproduce with TE.
Among several studies assessing bladder reconstruction with exogenous biomaterials, the Atala's group achieved excellent results in seven patients, aged 4-19 years, suffering from myelomeningocele . These patients needed augmentation cystoplasty, as they had severe urinary incontinence because of their neuropathic bladders (high-pressure or poorly compliant). Their bladders were reconstructed using a collagen scaffold seeded with patient's own bladder cells either with or without omental coverage, or a combined poly-glycolic acid (PGA)-collagen scaffold covered with omentum. The three patients with the composite collagen-PGA scaffold plus omental wrap showed better results, with several improvements in terms of preoperative values: bladder filling pressures decreased 56%, while the volume and the compliance increased 1.58-fold and 2.79-fold, respectively. After a mean follow-up of 46 months, no metabolic consequences and renal stones were noted and the mucous production and renal function remained normal. At last, the engineered bladders biopsies showed an adequate structural architecture and phenotype.
Despite this excellent outcome, during the phase II of a clinical study on eleven pediatric patients treated with the PGA matrix seeded with autologous urothelial cells, there was no clinical or statistical improvement in bladder capacity and compliance after a mean follow-up of 36 months. Adverse events, such as bladder rupture (n=3) and bowel obstruction (n=3), occurred in most of the patients and needed to be treated through other surgeries . The failure of this clinical study could be explained considering the disease condition of the bladder which offered poor status cells to seed onto scaffolds. In this way, it was demonstrated that the use of artificial urinary bladder is still far from replacing the classic use of GI tissue for augmentation cystoplasty.
Another solution, which was first reported in rats after partial cystectomy, is the use of bladder acellular matrix (BAM), prepared by removing mechanically and chemically cellular components from bladder tissue . Despite many years of intense research, BAM alone had never been able to achieve full bladder regeneration, as muscle layers developed incompletely . Therefore, BAM is being associated with stem cells to improve tissue regeneration [Figure 1] .
|Figure 1: Images of BAM seeded with MSCs from human umbilicus taken by Scanning Electron Microscope (SEM). A At 5 days the cells migrate and proliferate inside BAM (magnification ×2400). B At 10 days MSCs from human umbilicus fill in the surface of BAM (magnification ×1200).|
Source: Yuan H, Zhuang Y, Xiong J, Zhi W, Liu L, Wei Q, Han P. Human umbilical mesenchymal stem cells-seeded bladder acellular matrix grafts for reconstruction of bladder defects in a canine model. PLoS One. 2013 Nov 20;8(11):e80959. doi: 10.1371/journal.pone.0080959. eCollection 2013.
Click here to view
Current available biomaterials for bladder TE are classified in biological and synthetic ones. In addition to acellular matrixes, other examples of biological scaffolds used for treating the bladder are primarily made of collagen and alginate; synthetic polymers include poly L-lactide (PLLA), PGA and silk derivatives instead . The advantages of BAM and biological materials are related to good bio-compatibility and biodegradability, while the processing of synthetic materials allows to obtain scaffolds with more reproducible and predictable physical behavior . Although bladder TE is a promising alternative to traditional approaches, no strong benefits emerged comparing several biomaterials introduced in experimental studies ,,. Along with the definition of an adequate biomaterial and scaffold, bladder TE has still many challenges to solve, such as the appropriate choice of animal models; each animal model presents, indeed, its own specificity . For example, the composition of rabbits urine conducted to the formation of bladder stones when the animal is subjected to exogenous bladder material implants . Moreover, larger animals have a similar anatomy to human body than rats or rabbits and this help in being as close as possible to human situation in clinical evaluation . Another issue of the studies reported in literature is the absence of a long follow-up characterized by the comparison with a control group treated with the gold standard treatment (GI tissues) . All these parameters need to be taken into account and they are fundamental to find the optimal procedures for bladder regeneration before considering the clinical application.
Besides the importance of preclinical study standardization, greater interest is being reserved to obtain adequate stem cells for urological tissue-engineered organs. In this respect, Bharadwaj et al.  derived stem cells from excreted urine and differentiated them into bladder urothelial and smooth muscle phenotypes, demonstrating a potential future perspective for urological care.
3.2. Blood Vessels
Blood vessels are a striking example of application of RM strategies for engineering tubular organs. Since tissue-engineered vessels could be useful for common and life-threatening vascular lesions, research has been advanced greatly ,.
A traditional TE approach is the construction of functional living vascular grafts outside the body by using 3 elements: cells, scaffolds and bioreactors. Among all the organs, artificial blood vessels are the ones that are significantly developed by means of bioreactors: devices or systems able to reproduce biochemical/biophysical stimuli as in a physiological conditions. Computer-controlled pulsatile bioreactors seem to be superior then the old ones as they could permit the adjustment over a range of pressure and pulse rates, thus making great improvements in vascular TE .
As an alternative to autologous grafts, also xenogeneic or synthetic materials had largely been used, but, besides lacking of growth potential (key feature with pediatric patients), they were related to an increased risk of stenosis, infection and thromboembolization ,24],.
Therefore, the right strategy proved to be the use of biodegradable scaffolds seeded with patient's own cells. In this way, the autograft does not provoke immune responses and it degrades itself, leaving new tissue instead of a foreign body. This technology had been tried not only in laboratory or in animal models, but even in clinical setting. Indeed, a tubular biodegradable scaffold, created with polycaprolactone-polylactic acid (PCL-PLA) copolymer, reinforced with woven PGA and seeded with endothelial cells, was implanted to substitute a stenosed pulmonary artery, repaired previously . The cells were obtained from patient's stem cells through a blood sample. The tissue-engineered vascular autograft (TEVA) was later placed in a bioreactor system to acclimatize it to the conditions of the body until implantation. Neither occlusion nor aneurism of TEVA was observed in the recipient 7 months after implantation. Subsequently to Shin'oka's successful approach, 25 extracardiac cavopulmonary connections with TEVA as a conduit were performed on pediatric patients with mean age of 5.5 years . Long-term follow-up at 4 years after implantation demonstrated no instances of graft-related mortality, no cases of aneurysm formation, graft rupture nor calcification. Only two death were reported from late cardiac failure. This first human clinical trial confirmed the efficiency of TEVA and the absence of adverse events, such as graft rupture or aneurismal change.
Even for tissue-engineered small diameter vessels (< 6 mm), their development had been complicated by either occlusion or thrombosis of the current strategies for long time . However, Kurobe et al. recently succeeded in the construction and implantation in mice of a tissue engineered vascular graft (TEVG) for small diameter arteries as shown in [Figure 2] .
|Figure 2: Comparison between TEVG implantation to sham group. A TEVG was made of biodegradable electrospun polylactic acid (PLA) nanofibers (length=3mm; inner luminal diameter 500-600 μm). B implantation of TEVG. The image shows inferior vena cava (IVC) and aorta (Ao). C Survival rate at 24 hours after surgery. < 10% of mice implanted with TEVG died within 24 hours after TEVG implantation because of bleeding or thrombosis. D Kaplan-Meier survival curve considering the 12 months of experiment. No significant statistical difference was highlighted between the two groups.|
Source: Kurobe H, Maxfield MW, Tara S, Rocco KA, Bagi PS, Yi T, et al. (2015) Development of Small Diameter Nanofiber Tissue Engineered Arterial Grafts. PLoS ONE 10(4): e0120328. doi: 10.1371/journal.pone.0120328.
Click here to view
Despite the promising clinical results with large diameter engineered vessels, there are still some significant problems to solve, from the choice of material, geometry and scaffold composition, which should be standardized, to the definition of an accurate process of sterilization, preservation and transport of engineered grafts.
Recently, the attention shifted towards scaffold-free blood vessels realized by the bioprinting technology. ,. The letter uses a computer-controlled printing device to deposit cell aggregates, cells and biomaterials or cells encapsulated in hydrogels into defined 3D geometries. In this case, blood vessels with different diameters and cell patterns were printed using spherical and cylindrical multicellular systems as bioink. Since the fabrication method resulted accurate, reliable and scalable, further studies are now required to take advantage of bioprinting benefits to obtain reproducible implantable blood vessels in the near future.
The skin is probably the best well-known engineered organ and the daily clinical application of artificial skin is not far at all. The clinical gold standard in full-thickness injuries treatment is an autologous split-thickness graft, which consists in the surgical removal and subsequent stretching of epidermis and superficial dermis from an undamaged skin site of the patient; the autograft is thus applied on the full-thickness wound or burn. However, in case of extensive injuries, donor sites for autografts harvesting are not available. Allografts could be an additional option, but they still suffer the need of immunosuppressive therapies. To overcome these inconvenient, many research groups worldwide focused their attention on creating bioengineered skin substituted ,,. Some of the commercially available dermo-biopolymer composites for clinical applications are listed in [Table 1] ,,,,,,.
|Table 1: Some of the commercially available skin substitutes that have been successfully used in clinical practice.|
Click here to view
In addition to the current commercial skin substitutes, different approaches has been developed to meet the demand of skin replacement. Among the most innovative solutions, bioprinting is emerging as a potential tool for skin TE applications. A printer designed to print skin cells onto burn wounds had recently been built and tested at the Wake Forest Institute for Regenerative Medicine (WFIRM) . Before printing, a scanner is used to determine wound size and depth to calibrate the use of the ink, which, actually, includes different kinds of skin cells, collected from a skin patch one-tenth the size of the burn. The same research team has recently worked on the possibility to use the amniotic fluid-derived stem cells (AFSCs) to wound treatment in a mouse model of skin regeneration . After two-week observation, the AFSCs deposited in a collagen/fibrin gels accelerated closure and re-epithelialization of full-thickness wounds in mice faster than gel-only controls and were as effective as bone marrow-derived mesenchymal stem cells (MSCs) treatments. Additionally, histological examinations showed that AFS cells induced stronger angiogenesis and blood vessel maturation compared with the other two groups. In conclusion, together with commercial skin substitutes, bioprinting approach will become an optimal treatment for burns and skin wounds without requiring a secondary surgical site (as in case of gold standard treatment) and without provoking the patient's immune response by using AFSCs.
The success of a tissue-engineered trachea is determined only by its ability to conduct air lifelong, becoming a sustainable biological conduit. Many attempts had been tried to create an artificial trachea, but none showed superior.
On March 2010, at Great Ormond Street Hospital, in London, a stem-cell based tissue-engineered trachea was implanted in a 12-year-old child, born with congenital long segment tracheal stenosis and pulmonary sling . After a brief stimulation by granulocyte colony stimulating factor (G-CSF), bone marrow mesenchymal stem cells (BMSCs) were obtained preoperatively and seeded onto a scaffold with patches of autologous epithelium. Human recombinant erythropoietin (EPO) was applied topically to stimulate angiogenesis, along with Transforming growth factor beta (TGF-β) to support chondrogenesis. The graft revascularized within 1 week after implantation. Epithelium restoration became evident after 1 year, while the graft did not have biomechanical strength focally until 18 months, without requiring any medical interventions. Moreover, 18 months after surgery, he performed a chest CT scan and ventilation-perfusion scan, which resulted normal. At 2 years follow-up, he had a functional airway and returned to school, after growing 11 cm in height.
This study represents an evolution in the development of tissue-engineered tracheas, representing the foundation for future clinical applications.
The eye presents some advantages that makes it as an optimal candidate for RM applications; in fact, it is easy to access in order to perform pre-treatment assessments and collect cells, it can be simply observed and evaluated during follow-up and it is an immune-privileged organ. However, the eye is composed by many different tissues, whose artificial reconstructions are at a different stage of research .
|Figure 3: Tissue engineered skin construct inserted into the mouse wound after the implantation (left) and on the 11th day (right), when the wound fully healed.|
Source: Michael S, Sorg H, Peck CT, Koch L, Deiwick A, Chichkov B, Vogt PM, Reimers K. Tissue engineered skin substitutes created by laser-assisted bioprinting form skin-like structures in the dorsal skin fold chamber in mice. PLoS One. 2013;8(3):e57741. doi: 10.1371/journal.pone.0057741. Epub 2013 Mar 4.
Click here to view
Among all tissues, cornea is at the highest research domain. Corneal scarring from trauma and inflammation disrupts vision for millions worldwide, but corneal transplantation, the primary therapy for corneal blindness, is unavailable to many affected individuals.
As an alternative to cadaveric corneas transplantation, transparent thin gelatin gel (TGG) scaffolds, functionalized with heparin, were fabricated to support transfer of cultured human corneal endothelial cells (HCECs). Through a small incision in the cornea, the scaffold was implanted in rabbits’eye and gradually integrated with the surrounding tissue .
Cellular therapy seems to offer a valid alternative as well. Stem cells from different sources had been isolated, expended in vitro, differentiated and proved to function as corneal cells in vivo. In [Figure 4], the results associated to the treatment of corneas burned by alkali and later seeded with MSCs in rats are shown . Moreover, Du et al. collected human stem cells and transplanted them into mice with genetically cloudy corneas, which, eventually, became transparent .
|Figure 4: MSCs improve corneal wound healing. A–D Fluorescein-stained corneas of the control group show reduced recovery in reference to group treated with MSCs. E Percentage analysis of fluorescein-stained corneas highlights a significant statistical difference between the two groups: MSC group stained in a very lower manner than the control group, confirming the acceleration of corneal wound healing.|
Source: Yao L, Li ZR, Su WR, Li YP, Lin ML, Zhang WX, Liu Y, Wan Q, Liang D. Role of mesenchymal stem cells on cornea wound healing induced by acute alkali burn. PLoS One. 2012;7(2):e30842. doi: 10.1371/journal.pone.0030842. Epub 2012 Feb 17.
Click here to view
In addition to these pre-clinical treatments, Holoclar®, a stem cell-based medical product for the repair of the outer layer of cornea damaged by chemical or physical injuries, has recently been approved by European Commission. The therapy is based on the biopsy of a tiny portion (min 1-2 mm2) of the undamaged limbus and its growth in laboratory using specific techniques. The limbus is located between the sclera, the white part of the eye, and the cornea, the front part of the eye, and it is rich in stem cells able to heal the damaged cornea. Through this system, a novel sheet of cornea can be developed and transplanted back onto the eye. The combination of Holoclar® and corneal transplants can restore a normal cornea for previously incurable, deep corneal burns.
Together with cornea, also retina is involved in different eyes disease such as retinitis pigmentosa, diabetic retinopathy and age-related macular degeneration (AMD). The latter is considered as the leading cause of vision loss among older people. AMD is multifactorial disease which interests retinal pigment epithelium degeneration and it ends with the damage of the retina central portion that, eventually, conducts to the patient's vision loss. The traditional therapy consists of drugs able to stop neovascularization, but not able to repair the precedent damage. For this reason, recent progress have been made in the field of cell therapies for RPE treatment, including the use of induced pluripotent stem cells (iPSCs) and embryonic stem cells (ESCs) .
In particular, at the end of 2014 in Japan, at the RIKEN Center for Developmental Biology, a 70-year-old woman, suffering from AMD, was treated by using iPSCs, taken by hers and transplanted as a 1.3-3 mm RPE mono-layer without the use of synthetic scaffolds or matrices . No complications appeared with the transplant surgery and a one-year monitoring period was set to evaluate the initial results of the research. The technology described above represents a real breakthrough and is able to give faith to all patients suffering from AMD.
Recently, an American stem cell-based company reported successful completion of two phase I/II clinical trials for human ES-derived RPE cell suspension transplanted in 18 patients suffering from Stargardt's disease or with AMD. No major adverse events and immune responses were noted in any patient over a mean 22 months follow-up .
In conclusion, stem cell-based therapy could represent an effective solution for the cure of retinal degenerative disease.
| 4. Conclusions|| |
Every 30 seconds a patient dies from diseases which could be treated with tissue replacement . A tissue engineering and regenerative medicine (TERM) approach could probably offer the definitive solution for children with congenital malformations, young soldiers disfigured in war and old people suffering from chronic invalidating diseases, which are burdening more and more heavily on world's national economies . As described before in detail, current researches are supporting valuable directions to improve clinical applications of TE ,,,,,,.
Researchers are asked to direct their efforts towards the translation of the many different laboratory findings into modern and viable therapies: a close collaboration between clinicians and other scientists (bioengineers, materials engineers, biologists) is mandatory to translate basic scientific discoveries in TERM therapies to help their spread. However, efficacy and efficiency of these new solutions must be carefully evaluated before clinical trials. Specifically, pre-clinical studies ought to be constructed according to the following principles:
- Enrollment of large samples;
- Use of tissue/organ constructs which present similar dimensions as human ones;
- Appropriate choice of animals models which should not report over-or under-estimations;
- Selection of pertinent bioreactors (specially for vessels) to improve the construction of the artificial organ by means of adequate stimuli;
- Use of diseased tissues and/or dysfunctional animal organs in view of clinical applications;
- Long follow-up;
- Comparisons with the gold standard treatment.
In order to stimulate reader's research interests, the authors would like to highlight major challenges which need to be solved in future:
- Vascularization and innervation of artificial constructs;
- Engineering organs with different cell types;
- Construction of validated bioreactors to avoid animal testing;
- Conducting appropriate pre-clinical and clinical trials following the principles indicated above in order to make TERM approach the gold standard treatment for every diseases.
When all these issues are completely overcome, TERM approach will become superior to existing clinical therapies.
| 5. Conflict of interest|| |
| References|| |
Sampogna G, Guraya SY, Forgione A. Regenerative medicine: Historical roots and potential strategies in modern medicine. JMAU September 2015;Volume 3(Issue 3):101-7.
Gardner J, Webster A. The social management of biomedical novelty: Facilitating translation in regenerative medicine. Social Science & Medicine 2016;156:90-7.
Alberti C. Tissue engineering technologies: just a quick note about transplantation of bioengineered donor trachea and augmentation cystoplasty by de novo engineered bladder tissue. Chir 2009;30:514-9.
Langer R, Vacanti J. Advances in tissue engineering. J Pediatr Surg 2016;51:8-12.
www.clinicaltrials.gov consulted for “Regenerative Medicine” trials on February 2016.
Nieuwenhuijzen JA, De Vries RR, Bex A, Van der Poel HG, Meinhardt W, Antonini N. Urinary diversion after cystectomy: the association of clinical factors, complications and functional results of four different diversion. Eur Urol 2008;53:834-42.
Atala A, Bauer SB, Soker S, Yoo JJ, Retik AB. Tissue-engineered autologou bladders for patients needing cystoplasty Lancet 2006;367(9518):1241-6.
Joseph DB, Borer JG, De Filippo RE, Hodges SJ, McLorie GA. Autologous cell seeded biodegradable scaffold for augmentation cystoplasty: phase II study in children and adolescents with spina bifida. J Urol 2014;191(5):1389-95.
Sutherland RS, Baskin LS, Hayward SW, Cunha GR. Regeneration of bladder urothelium, smooth muscle, blood vessels and nerves into an acellulartissue matrix. J Urol 1996;156(2):571-7.
Jayo MJ, Jain D, Ludlow JW, Payne R, Wagner B, McLoire G, et al. Long-term durability, tissue regeneration and neo-organ growth during skeletal maturation with a neo-bladder augmentation construct. Regen Med 2008;3(5):671-82.
Yuan H, Zhuang Y, Xiong J, Zhi W, Liu L, Wei Q, et al. Human umbilical mesenchymal stem cells-seeded bladder acellular matrix grafts for reconstruction of bladder defects in a canine model. PLoS ONE 2013;8(11):e80959.
Lam Van Ba O, Aharony S, Loutochin O, Corcos J. Bladder tissue engineering: A literature review. Advanced Drug Delivery Reviews 2015;82-83:31-7.
Chapple CR, Osman N, Mangera A, Hillary C, Roman S, Bullock A, et al. Application of tissue engineering to pelvic organ prolapse and stress urinary incontinence. LUTS 2015;7:63-70.
Sloff M, De Vries R, Geutjes P, IntHout J, Ritskes-Hoitinga M, Ooster-wijk E. Tissue engineering in animal models for urinary diversion: a systematic review. PLoS ONE 2014;9(6):e98734.
Nuininga JE, van Moerkerk H, Hanssen A, Hulsbergen CA, Oosterwijk-Wakka J, Oosterwijk E, et al. A rabbit model to tissue engineer the bladder. Biomaterials 2004;25:1657-61.
Roth CC, Mondalek FG, Kibar Y, Ashley RA, Bell CH, Califano JA, et al. Bladder regeneration in a canine model using hyaluronic acid-poly(lactic-co-glycolicacid) nanoparticle modified porcine small intestinal submucosa. BJU 2011;108:148-55.
Sloff M, Simaioforidis V, De Vries R, Oosterwijk E, Feitz W. Tissue Engineering of the Bladder - Reality or Myth? A Systematic Review. J Urol 2014;192(4):1035-42.
Bharadwaj S1, Liu G, Shi Y, Wu R, Yang B, He T, et al. Multipotential differentiation of human urine-derived stem cells:potential for therapeutic applications in urology. Stem Cells 2013;31(9):1840-56.
Li S, Sengupta D, Chien S. Vascular tissue engineering: from in vitro
to in situ
. WIREs Syst Biol Med 2014;6:61-76.
Zou T, Fan J, Fartash A, Liu H, Fan Y. Cell-based strategies for vascular regeneration. J Biomed Mater Res A 2016;00A(00):1-18.
Song L, Zhou Q, Duan P, Guo P, Li D, Xu Y, et al. Successful development of small diameter tissue-engineering vascular vessels by our novel integrally designed pulsatile perfusion-based bioreactor. PLoS ONE 2014;7(8):e42569.
Deutsch M, Meinhart J, Fischlein T, Preiss P, Zilla P. Clinical autoloous in vitro endothelialization of infrainguinal ePTFE grafts in 100 patients: a 9-Year experience. Surgery 1999;126:847-55.
Gabbieri D, Dohmen PM, Koch C, Lembcke A, Rutsch W, Konertz W. Aortocoronaty endothelial cell-seeded polytetrafluoroethylene graft: 9-Year patency. Ann Thorac Surg 2007;83:1166-8.
Matsumura G, Miyagawa-Tomita S, Shin’oka T, Ikada Y, Kurosawa H. First evidence that bone marrow cells contribute to the construction of tissue-engineered vascular autografts in vivo. Circulation 2003;108:1729-34.
Shin’oka T, Imai Y, Ikada Y. Transplantation of a tissue-engineered pulmonary artery. N. Engl. J. Med 2001;344:532-3.
Kurobe H, Maxfield MW, Breuer CK, Shin’oka T. Concise review: tissue-engineered vascular grafts for cardiac surgery: past, present, and future. Stem Cells Transl. Med 2012;1:566-71.
Peck M, Gebhart D, Dusserre N, McAllister TN, L’Heureux N. The evolution of vascular tissue engineering and current state of the art. Cells, tissues, organs 2012;195(1–2):144-58.
Norotte C, Marga F, Niklason L, Forgacs G. Scaffold-Free Vascular Tissue Engineering Using Bioprinting. Biomaterials 2009;30(30):5910-7.
Shafiee A, Atala A. Printing Technologies for Medical Applications. Trends in Molecular Medicine 2016;22(3):254-65.
Shevchenko RV, James SL, James SE. A review of tissue-engineered skin bio constructs available for skin reconstruction. J.R. Soc. Interface 2010;7:229-58.
Halim AS, Khoo TL, Shah JM. Biologic and synthetic skin substitutes: An overview. Indian J Plast Surg 2010;43(Suppl S1):23-30.
Lepow BD, Downey M, Yurgelon J, Klassen L, Armstrong DG. Bioengineered tissues in wound healing. Expert Rev Dermatol 2011;6(3):255-62.
Hart CE, Loewen-Rodriguez A, Lessem J. Dermagraft: Use in the Treatment of Chronic Wounds. Advances in Wound Care 2012;1(3):138-41.
Falanga V, Sabolinski ML. A bilayered living skin construct (Apligraf®) accelerates complete closure of hard-to-heal venous ulcers. Wound Repair Regen 1999;7:201-7.
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;29:837-41.
Caravaggi C, De Giglio R, Pritelli C, Sommaria M, Della Noce S, Faglia E, et al. HYAFF 11–Based autologous dermal and epidermal grafts in the treatment of non-infected diabetic plantar and dorsal foot ulcers. Diabetes Care 2003;26(10):2853-9.
Uccioli L. A clinical investigation on the characteristics and outcomes of treating chronic lower extremity wounds using the tissue tech autograft system. Int. J. Low Extrem. Wounds 2003;2:140-51.
Michael S, Sorg H, Peck CT, Koch L, Deiwick A, Chichkov B, et al. Tissue engineered skin substitutes created by laser-assisted bioprinting form skin-like structures in the dorsal skin fold chamber in mice. PLoS ONE 2013;8(3):e57741.
Min JH, Yun IS, Lew DH, Roh TS, Lee WJ. The use of Matriderm and autologous skin graft in the treatment of full thickness skin defects. Arch Plast Surg 2014;41(4):330-6.
Murphy SV, Atala A. 3D bioprinting of tissues and organs. Nat. Biotechnol 2014;32(8):773-85.
Skardal A, Mack D, Kapetanovic E, Anthony Atala A, Jackson JD, Yoo J, et al. Bioprinted Amniotic Fluid-Derived Stem Cells Accelerate Healing of Large Skin Wounds. Stem Cells Transl. Med 2012 Nov;1(11):792-802.
Elliott MJ, De Coppi P, Speggiorin S, Roebuck D, Butler CR, Samuel E, et al. Stem-cell-based, tissue engineered tracheal replacement in a child: a 2-year follow-up study. Lancet 2012;380(9846): 994-1000.
Elisseeff J, Madrid MG, Lu Q, Chae JJ, Guo Q. Future Perspectives for Regenerative Medicine in Ophthalmology. Middle East Afr. J. Oph-thalmol 2013;20(1):38-45.
Niu G, Choi JS, Wang Z, Skardal A, Giegengack M, Soker S. Heparin-modified gelatin scaffolds for human corneal endothelial cell transplantation. Biomaterials 2014;35(13):4005-14.
Yao L, Li ZR, Su WR, Li YP, Lin ML, Zhang WX, et al. Role of Mesenchymal Stem Cells on Cornea Wound Healing Induced by Acute Alkali Burn. PLoS ONE 2012;7(2):e30842.
Du Y, Carlson EC, Funderburgh ML, Birk DE, Pearlman E, Guo N, et al. Stem Cell Therapy Restores Transparency to Defective Murine Corneas. Stem Cells 2009;27(7):1635-42.
Schwartz SD, Regillo CD, Lam BL, Eliott D, Rosenfeld PJ, Gregori NZ, et al. Human embryonic stem cell-derived retinal pigment epithelium in patients with age-related macular degeneration and Stargardt's macular dystrophy: follow-up of two open-label phase 1/2 studies. Lancet 2015;385:509-16.
Anthony, Atala. Growing new organs. TEDMED Event Jan 2010.
The 2012 OASDI Trustees Report. Table IV.B2.
[Figure 1], [Figure 2], [Figure 3], [Figure 4]
|This article has been cited by|
||MR and PET-CT monitoring of tissue-engineered vascular grafts in the ovine carotid artery
| ||Frederic Wolf,Vera Paefgen,Oliver Winz,Marianne Mertens,Sabine Koch,Nicolas Gross-Weege,Agnieszka Morgenroth,Anne Rix,Heike Schnoering,Khaled Chalabi,Stefan Jockenhoevel,Twan Lammers,Felix Mottaghy,Fabian Kiessling,Petra Mela |
| ||Biomaterials. 2019; : 119228 |
|[Pubmed] | [DOI]|
||Bibliographic review on the state of the art of strontium and zinc based regenerative therapies. Recent developments and clinical applications
| ||Mirta Jimťnez,Cristina Abradelo,Julio San RomŠn,Luis Rojo |
| ||Journal of Materials Chemistry B. 2019; |
|[Pubmed] | [DOI]|
||Devising tissue ingrowth metrics: a contribution to the computational characterization of engineered soft tissue healing
| ||Antoine Alves,Nina Attik,Yves Bayon,Elodie Royet,Carine Wirth,Xavier Bourges,Alexis Piat,GaŽlle Dolmazon,GaŽlle Clermont,Jean-Pierre Boutrand,Brigitte Grosgogeat,Kerstin Gritsch |
| ||Biomedical Materials. 2018; 13(3): 035010 |
|[Pubmed] | [DOI]|
||Advances in perinatal stem cells research: a precious cell source for clinical applications
| ||Bahareh Abbaspanah,Maryam Momeni,Marzieh Ebrahimi,Seyed Hadi Mousavi |
| ||Regenerative Medicine. 2018; |
|[Pubmed] | [DOI]|