⚠ Official Notice: www.ijisrt.com is the official website of the International Journal of Innovative Science and Research Technology (IJISRT) Journal for research paper submission and publication. Please beware of fake or duplicate websites using the IJISRT name.



Mesenchymal Stem Cells and their Derivatives in Normal and Diabetic Wound Healing: Mechanisms, Therapeutic Advances, and Clinical Translation; A Systematic Review


Authors : Abhishek Kumar; Dr. Jitesh Kumar; Arun Singha

Volume/Issue : Volume 11 - 2026, Issue 7 - July


Google Scholar : https://tinyurl.com/r48d2awe

Scribd : https://tinyurl.com/2j9z8vu8

DOI : https://doi.org/10.38124/ijisrt/26jul431

Note : A published paper may take 4-5 working days from the publication date to appear in PlumX Metrics, Semantic Scholar, and ResearchGate.


Abstract : Chronic wounds such as DFUs present an important problem in modern medicine because of chronic inflammation, poor angiogenesis, oxidative stress, and abnormal extracellular matrix remodelling, which interfere with wound healing. Stem cells, especially mesenchymal stem cells (MSCs), have attracted considerable attention due to their capability to regulate inflammation, stimulate angiogenesis, increase collagen production, support re-epithelialization, and manage immune response mainly through paracrine action. This systematic review was undertaken to assess the biological mechanisms, therapeutic potential, and translational value of MSCs and MSC-derived products (extracellular vesicles, exosomes, secretome, conditioned medium) in the process of normal and diabetic wound healing. The search strategy and inclusion criteria for the review were designed in accordance with PRISMA 2020 guidelines and were performed on PubMed/MEDLINE, Scopus, Web of Science, Embase, and ClinicalTrials.gov databases. Altogether, eleven eligible preclinical and clinical studies were included in a qualitative analysis. Because of the high level of heterogeneity in design, cell source, mode of administration, and outcomes, the meta-analysis could not be performed. All included studies revealed positive effects of MSC-based treatment on wound closure, angiogenesis, granulation tissue formation, collagen production, oxidative stress decrease, and pro-inflammatory macrophage polarisation modulation. MSC-derived cell-free therapy, especially exosomes and secretome, replicated the reparative effects of their parent cells and provided additional benefits like decreased immunogenicity, enhanced biosafety and ease of manufacturing. In addition, cell retention and sustained effect of therapeutic delivery were achieved through biomaterial-based systems such as hydrogels, nanofibers, injectable systems, and smart dressings. Even though the initial results from the clinical trials suggest promising safety and efficacy in chronic wound healing, there are several hurdles to be overcome, such as standardisation, manufacturing, regulatory approval, and clinical validation. Nevertheless, MSC and cell-free therapies seem to hold great potential in wound repair, especially in diabetic foot ulcers, and require further testing in RCTs before clinical use

Keywords : Mesenchymal Stem Cells, Wound Healing, Diabetic Foot Ulcer, Exosomes, Extracellular Vesicles, Regenerative Medicine, Cell-Free Therapy.

References :

  1. Martin P. Wound healing—aiming for perfect skin regeneration. Science. 1997;276(5309):75–81. doi:10.1126/science.276.5309.75.
  2. Gurtner GC, Werner S, Barrandon Y, Longaker MT. Wound repair and regeneration. Nature. 2008;453(7193):314–321. doi:10.1038/nature07039.
  3. Armstrong DG, Boulton AJM, Bus SA. Diabetic foot ulcers and their recurrence. N Engl J Med. 2017;376(24):2367–2375. doi:10.1056/NEJMra1615439.
  4. Brem H, Tomic-Canic M. Cellular and molecular basis of wound healing in diabetes. J Clin Invest. 2007;117(5):1219–1222. doi:10.1172/JCI32169.
  5. Falanga V. Wound healing and its impairment in the diabetic foot. Lancet. 2005;366(9498):1736–1743. doi:10.1016/S0140-6736(05)67792-3.
  6. Frykberg RG, Banks J. Challenges in the treatment of chronic wounds. Adv Wound Care. 2015;4(9):560–582. doi:10.1089/wound.2015.0635.
  7. Pittenger MF, Mackay AM, Beck SC, et al. Multilineage potential of adult human mesenchymal stem cells. Science. 1999;284(5411):143–147. doi:10.1126/science.284.5411.143.
  8. Dominici M, Le Blanc K, Mueller I, et al. Minimal criteria for defining multipotent mesenchymal stromal cells. Cytotherapy. 2006;8(4):315–317. doi:10.1080/14653240600855905.
  9. Caplan AI, Dennis JE. Mesenchymal stem cells as trophic mediators. J Cell Biochem. 2006;98(5):1076–1084. doi:10.1002/jcb.20886.
  10. Maxson S, Lopez EA, Yoo D, Danilkovitch-Miagkova A, Leroux MA. Concise review: role of mesenchymal stem cells in wound repair. Stem Cells Transl Med. 2012;1(2):142–149. doi:10.5966/SCTM.2011-0018.
  11. Hu MS, Borrelli MR, Lorenz HP, Longaker MT, Wan DC. Mesenchymal stromal cells and cutaneous wound healing: a comprehensive review. Stem Cells Int. 2018;2018:6901983. doi:10.1155/2018/6901983.
  12. Shi Y, Wang Y, Li Q, et al. Immunoregulatory mechanisms of mesenchymal stem and stromal cells. Nat Rev Nephrol. 2018;14(8):493–507. doi:10.1038/s41581-018-0029-5.
  13. Vizoso FJ, Eiro N, Cid S, Schneider J, Perez-Fernandez R. Mesenchymal stem cell secretome. Int J Mol Sci. 2017;18(9):1852. doi:10.3390/ijms18091852.
  14. Phinney DG, Pittenger MF. Concise review: MSC-derived exosomes. Stem Cells. 2017;35(4):851–858. doi:10.1002/stem.2575.
  15. Toh WS, Lai RC, Hui JHP, Lim SK. MSC exosome as a cell-free therapy. Stem Cell Res Ther. 2018;9:225. doi:10.1186/s13287-018-0988-7.
  16. Eming SA, Martin P, Tomic-Canic M. Wound repair and regeneration: mechanisms, signalling, and translation. Sci Transl Med. 2014;6(265):265sr6. doi:10.1126/scitranslmed.3009337.
  17. Page MJ, McKenzie JE, Bossuyt PM, et al. The PRISMA 2020 statement. BMJ. 2021;372:n71. doi:10.1136/bmj.n71.
  18. Sterne JAC, Savović J, Page MJ, et al. RoB 2 tool. BMJ. 2019;366:l4898. doi:10.1136/bmj.l4898.
  19. Hooijmans CR, Rovers MM, de Vries RBM, et al. SYRCLE's risk of bias tool. BMC Med Res Methodol. 2014;14:43. doi:10.1186/1471-2288-14-43.
  20. Caplan AI. Mesenchymal stem cells: time to change the name! Stem Cells Transl Med. 2017;6(6):1445–1451. doi:10.1002/sctm.17-0051.
  21. Song HB, Park SY, Ko JH, et al. MSCs promote M2 macrophage polarization. Exp Mol Med. 2017;49:e253. doi:10.1038/emm.2016.135.
  22. English K. Mechanisms of MSC immunomodulation. Immunol Cell Biol. 2013;91(1):19–26. doi:10.1038/icb.2012.56.
  23. Chen L, Tredget EE, Wu PYG, Wu Y. Paracrine factors recruit macrophages and endothelial cells. PLoS One. 2008;3:e1886. doi:10.1371/journal.pone.0001886.
  24. Kinnaird T, Stabile E, Burnett MS, Epstein SE. Paracrine mechanisms of neovascularization. Circ Res. 2004;94(5):678–685. doi:10.1161/01.RES.0000118491.36445.B7.
  25. Wu Y, Chen L, Scott PG, Tredget EE. Mesenchymal stem cells enhance wound healing. Stem Cells. 2007;25(10):2648–2659. doi:10.1634/stemcells.2007-0226.
  26. Caley MP, Martins VLC, O'Toole EA. Metalloproteinases and wound healing. Adv Wound Care. 2015;4:225–234. doi:10.1089/wound.2014.0581.
  27. Sasaki M, Abe R, Fujita Y, Ando S, Inokuma D, Shimizu H. Mesenchymal stem cells promote epidermal regeneration. Wound Repair Regen. 2008;16:254–265. doi:10.1111/j.1524-475X.2008.00359.x.
  28. Li X, Xie X, Yu Z, et al. Nrf2 signaling and oxidative stress regulation in wound healing. Free Radic Biol Med. 2019;139:208–220. doi:10.1016/j.freeradbiomed.2019.05.032.
  29. Zhang B, Wang M, Gong A, et al. HucMSC-exosome-mediated Wnt/β-catenin signaling promotes wound healing. Stem Cell Res Ther. 2015;6:229. doi:10.1186/s13287-015-0237-0.
  30. Théry C, Zitvogel L, Amigorena S. Exosomes: composition, biogenesis and function. Nat Rev Immunol. 2002;2:569–579. doi:10.1038/nri855.
  31. Yáñez-Mó M, Siljander PRM, Andreu Z, et al. Biological properties of extracellular vesicles and their physiological functions. J Extracell Vesicles. 2015;4:27066. doi:10.3402/jev.v4.27066.
  32. Lai RC, Yeo RWY, Lim SK. Mesenchymal stem cell exosomes. Semin Cell Dev Biol. 2015;40:82–88. doi:10.1016/j.semcdb.2015.03.001.
  33. Ferguson SW, Nguyen J. Exosomes as therapeutics. ACS Nano. 2016;10:2189–2198. doi:10.1021/acsnano.5b07677.
  34. Ti D, Hao H, Tong C, et al. LPS-preconditioned MSC-derived exosomes attenuate inflammation. Stem Cell Res Ther. 2015;6:188. doi:10.1186/s13287-015-0177-8.
  35. Song Y, Dou H, Li X, et al. Exosomal miR-146a contributes to anti-inflammatory activity. Stem Cells. 2017;35:1208–1221. doi:10.1002/stem.2564.
  36. Zhang B, Wang M, Gong A, Zhang X, Wu X, Zhu Y, Shi H, Wu L, Zhu W, Qian H, Xu W. HucMSC-exosome-mediated Wnt4 signaling is required for cutaneous wound healing. Stem Cell Research & Therapy. 2015;6:229. doi:10.1186/s13287-015-0237-0.
  37. Shabbir A, Cox A, Rodriguez-Menocal L, et al. Mesenchymal stem cell exosomes induce proliferation and migration of fibroblasts and endothelial cells. Stem Cells Dev. 2015;24:1635–1647. doi:10.1089/scd.2014.0316.
  38. Ferreira JR, Teixeira GQ, Santos SG, et al. Mesenchymal stromal cell secretome: influencing therapeutic potential. Stem Cells Int. 2018;2018:7538754. doi:10.1155/2018/7538754.
  39. Pawitan JA. Prospect of stem cell conditioned medium in regenerative medicine. Biomed Res Int. 2014;2014:965849. doi:10.1155/2014/965849.
  40. Walter MNM, Wright KT, Fuller HR, et al. Mesenchymal stem cell-conditioned medium accelerates wound healing. Wound Repair Regen. 2010;18:18–27. doi:10.1111/j.1524-475X.2009.00546.x.
  41. Théry C, Witwer KW, Aikawa E, et al. Minimal information for studies of extracellular vesicles 2018 (MISEV2018). J Extracell Vesicles. 2018;7:1535750. doi:10.1080/20013078.2018.1535750.
  42. Loots MAM, Lamme EN, Zeegelaar J, et al. Differences in cellular infiltrate and extracellular matrix of chronic diabetic and venous ulcers versus acute wounds. J Invest Dermatol. 1998;111:850–857. doi:10.1046/j.1523-1747.1998.00415.x.
  43. Gallagher KA, Liu ZJ, Xiao M, et al. Diabetic impairments in NO-mediated endothelial progenitor cell mobilization and HIF-1α stabilization. Proc Natl Acad Sci USA. 2007;104:19167–19172. doi:10.1073/pnas.0705853104.
  44. Bitar MS. Diabetes-induced oxidative stress and delayed wound healing. J Diabetes Complications. 2012;26:210–215. doi:10.1016/j.jdiacomp.2012.03.001.
  45. Yuan Y, Zhang Y, Han S, et al. Mesenchymal stem cell-derived exosomes alleviate oxidative stress through SIRT1 pathways. Stem Cell Res Ther. 2020;11:182. doi:10.1186/s13287-020-01673-9.
  46. Murphy MB, Moncivais K, Caplan AI. Mesenchymal stem cells: environmentally responsive therapeutics. Exp Mol Med. 2013;45:e54. doi:10.1038/emm.2013.94.
  47. Zhao X, Wu H, Guo B, Dong R, Qiu Y, Ma PX. Antibacterial anti-oxidant electroactive injectable hydrogel promotes skin wound healing. Biomaterials. 2017;122:34-47. doi:10.1016/j.biomaterials.2017.01.011.
  48. Annabi N, Tamayol A, Uquillas JA, et al. 25th anniversary article: rational design and applications of hydrogels in regenerative medicine. Adv Mater. 2014;26:85-124. doi:10.1002/adma.201303233.
  49. Ahmed EM. Hydrogel: preparation, characterization, and applications. J Adv Res. 2015;6:105-121. doi:10.1016/j.jare.2013.07.006.
  50. Rustad KC, Wong VW, Sorkin M, et al. Enhancement of mesenchymal stem cell survival in diabetic wounds. Sci Transl Med. 2012;4:173ra47. doi:10.1126/scitranslmed.3005307.
  51. Wang C, Wang M, Xu T, et al. Engineering bioactive self-healing antibacterial exosome hydrogels for diabetic wound healing. Adv Funct Mater. 2019;29:1904808. doi:10.1002/adfm.201904808.
  52. Xue J, Xie J, Liu W, Xia Y. Electrospun nanofibers for wound healing. Adv Drug Deliv Rev. 2019;146:214-230. doi:10.1016/j.addr.2018.12.001.
  53. Choi JS, Kim BS, Kim JY, et al. Decellularized extracellular matrix scaffolds for tissue engineering. Biomaterials. 2013;34:3571-3584. doi:10.1016/j.biomaterials.2013.01.070.
  54. Kai D, Wang QL, Wang HJ, et al. Stem cell-loaded nanofibrous scaffolds for tissue regeneration. Biomaterials. 2014;35:6016-6027. doi:10.1016/j.biomaterials.2014.04.036.
  55. Unnithan AR, Gnanasekaran G, Sathishkumar Y, et al. Electrospun antibacterial wound dressings. Int J Biol Macromol. 2014;67:1-11. doi:10.1016/j.ijbiomac.2014.03.014.
  56. Yang J, Yamato M, Kohno C, et al. Cell sheet engineering for regenerative medicine. Biomaterials. 2005;26:6415-6422. doi:10.1016/j.biomaterials.2005.04.061.
  57. Cerqueira MT, Pirraco RP, Santos TC, et al. Human adipose stem cell sheets in wound healing. Stem Cell Res Ther. 2013;4:110. doi:10.1186/scrt328.
  58. Tandara AA, Mustoe TA. Oxygen in wound healing. World J Surg. 2004;28:294-300. doi:10.1007/s00268-003-7400-2.
  59. Guan G, Niu X, Wang Y, et al. Oxygen-releasing biomaterials combined with stem cells improve diabetic wound healing. Biomaterials. 2021;269:120673. doi:10.1016/j.biomaterials.2020.120673.
  60. Sen CK. Wound healing essentials. Adv Wound Care. 2019;8:39-53. doi:10.1089/wound.2017.0745.
  61. Dash NR, Dash SN, Routray P, Mohapatra S, Mohapatra PC. Targeting nonhealing ulcers with autologous bone marrow-derived mesenchymal stem cells. Stem Cells Int. 2009;2009:1-9. doi:10.4061/2009/165327.
  62. King AJF. The use of animal models in diabetes research. Br J Pharmacol. 2012;166:877-894. doi:10.1111/j.1476-5381.2012.01911.x.
  63. Fang RC, Kryger ZB, Buck DW, et al. Limitations of the db/db mouse model in diabetic wound healing studies. Plast Reconstr Surg. 2010;126:1170-1177. doi:10.1097/PRS.0b013e3181ea44b0.
  64. Sullivan TP, Eaglstein WH, Davis SC, Mertz P. The pig as a model for human wound healing. Wound Repair Regen. 2001;9:66-76. doi:10.1046/j.1524-475x.2001.00066.x.
  65. Zuk PA, Zhu M, Mizuno H, et al. Multilineage cells from human adipose tissue. Tissue Eng. 2001;7:211-228. doi:10.1089/107632701300062859.
  66. Kim WS, Park BS, Sung JH, et al. Wound healing effect of adipose-derived stem cells. Stem Cells. 2007;25:1814-1821. doi:10.1634/stemcells.2006-0540.
  67. Wang HS, Hung SC, Peng ST, et al. Mesenchymal stem cells in the Wharton's jelly of the human umbilical cord. Stem Cells. 2004;22:1330-1337. doi:10.1634/stemcells.2004-0013.
  68. Arno AI, Amini-Nik S, Blit PH, et al. Human Wharton's jelly MSCs promote skin wound healing. Stem Cell Res Ther. 2014;5:28. doi:10.1186/scrt417.
  69. Squillaro T, Peluso G, Galderisi U. Clinical trials with mesenchymal stem cells: an update. Cell Transplant. 2016;25(5):829–848. doi:10.3727/096368915X689622.
  70. Ntege EH, Sunami H, Shimizu Y. Advances in regenerative therapy using mesenchymal stem cells. Stem Cells Int. 2020;2020:8831718. doi:10.1155/2020/8831718.
  71. Daley GQ. Stem cells and regenerative medicine. N Engl J Med. 2012;366(25):2396–2397. doi:10.1056/NEJMcibr1203740.
  72. Procházka V, Gumulec J, Jalůvka F, Salounová D, Jonszta T, Czerný D, et al. Cell therapy, a new standard in management of chronic critical limb ischemia and diabetic foot ulcer. Cell Transplant. 2010;19(11):1413–1424. doi:10.3727/096368910X514315.
  73. Lu D, Chen B, Liang Z, Deng W, Jiang Y, Li S, et al. Comparison of bone marrow mesenchymal stem cells with bone marrow mononuclear cells for treatment of diabetic critical limb ischemia. Diabetes Res Clin Pract. 2011;92(1):26–36. doi:10.1016/j.diabres.2010.12.010.
  74. Moon KC, Suh HS, Kim KB, Han SK, Young KW, Lee JW, et al. Potential of allogeneic adipose-derived stem cell-hydrogel complex for treating diabetic foot ulcers. Stem Cells Transl Med. 2019;8(12):1252–1262. doi:10.1002/sctm.18-0292.
  75. Lee HC, An SG, Lee HW, Park JS, Cha KS, Hong TJ, et al. Safety and effect of adipose tissue-derived stem cell implantation in patients with critical limb ischemia. Stem Cells Transl Med. 2018;7(3):229–238. doi:10.1002/sctm.17-0186.
  76. Xie B, Chen J, Liu B, Zhan J. Stem cell therapy for diabetic foot ulcers: a meta-analysis. Stem Cell Res Ther. 2017;8:39. doi:10.1186/s13287-017-0491-7.
  77. Qiu X, Liu J, Zheng C, Su Y, Bao L, Zhu B, et al. Mesenchymal stem cell therapy for diabetic foot ulcers: a systematic review and meta-analysis. BMJ Open Diabetes Res Care. 2020;8:e001778. doi:10.1136/bmjdrc-2020-001778.
  78. Gao Y, Liu Z, Chen Y, et al. Efficacy and safety of mesenchymal stem cell therapy in diabetic foot ulcer treatment: a systematic review and meta-analysis. Front Endocrinol (Lausanne). 2022;13:961819. doi:10.3389/fendo.2022.961819.
  79. Lalu MM, McIntyre L, Pugliese C, Fergusson D, Winston BW, Marshall JC, et al. Safety of cell therapy with mesenchymal stromal cells. PLoS One. 2012;7(10):e47559. doi:10.1371/journal.pone.0047559.
  80. Galipeau J, Sensébé L. Mesenchymal stromal cells: clinical challenges and therapeutic opportunities. Cytotherapy. 2018;20(5):524–539. doi:10.1016/j.jcyt.2018.01.001.
  81. Le Blanc K, Davies LC. Mesenchymal stromal cells and the innate immune response. Immunol Lett. 2015;168(2):140–146. doi:10.1016/j.imlet.2015.05.004.
  82. Thompson M, Mei SHJ, Wolfe D, Champagne J, Fergusson D, Stewart DJ, et al. Cell therapy with mesenchymal stromal cells: safety and efficacy. Stem Cells Transl Med. 2020;9(12):1568–1588. doi:10.1002/sctm.19-0326.
  83. Barkholt L, Flory E, Jekerle V, Lucas-Samuel S, Ahnert P, Bisset L, et al. Risk of tumorigenicity in mesenchymal stromal cell-based therapies. Cytotherapy. 2013;15(7):753–767. doi:10.1016/j.jcyt.2013.03.005.
  84. Sensebé L, Bourin P. Mesenchymal stem cells for therapeutic purposes. Transplantation. 2009;87(9 Suppl):S49–S53. doi:10.1097/TP.0b013e3181a285db.
  85. Higgins JPT, Thomas J, Chandler J, Cumpston M, Li T, Page MJ, Welch VA. Cochrane Handbook for Systematic Reviews of Interventions. 2nd ed. Wiley; 2019.
  86. Page MJ, Higgins JPT, Sterne JAC. Assessing risk of bias due to missing results in a synthesis. Cochrane Database Syst Rev. 2019;10:MR000042. doi:10.1002/14651858.MR000042.pub2.
  87. Cuende N, Rasko JEJ, Koh MBC, Dominici M, Ikonomou L. Cell, tissue and gene products with marketing authorization in Europe and the United States. Cytotherapy. 2018;20(11):1401–1413. doi:10.1016/j.jcyt.2018.09.010.
  88. Marks PW, Witten CM, Califf RM. Clarifying stem-cell therapy's benefits and risks. N Engl J Med. 2017;376(11):1007–1009. doi:10.1056/NEJMp1613723.
  89. Estrada JC, Albo C, Benguría A, Dopazo A, López-Romero P, Carrera-Quintanar L, et al. Culture conditions affect the biological properties of human mesenchymal stem cells. Stem Cells Dev. 2012;21(7):1071–1084. doi:10.1089/scd.2011.0398.
  90. Giebel B, Hermann DM. Identification of the right extracellular vesicle-based product for therapeutic use. Stem Cells Int. 2019;2019:1–14. doi:10.1155/2019/1053130.
  91. Heathman TRJ, Nienow AW, McCall MJ, Coopman K, Kara B, Hewitt CJ. The translation of cell-based therapies: clinical landscape and manufacturing challenges. Stem Cells Transl Med. 2015;4(5):389–398. doi:10.5966/sctm.2014-0266.
  92. Stolzing A, Jones E, McGonagle D, Scutt A. Age-related changes in human bone marrow-derived mesenchymal stem cells: consequences for cell therapies. Mech Ageing Dev. 2008;129(3):163–173. doi:10.1016/j.mad.2007.12.002.

Chronic wounds such as DFUs present an important problem in modern medicine because of chronic inflammation, poor angiogenesis, oxidative stress, and abnormal extracellular matrix remodelling, which interfere with wound healing. Stem cells, especially mesenchymal stem cells (MSCs), have attracted considerable attention due to their capability to regulate inflammation, stimulate angiogenesis, increase collagen production, support re-epithelialization, and manage immune response mainly through paracrine action. This systematic review was undertaken to assess the biological mechanisms, therapeutic potential, and translational value of MSCs and MSC-derived products (extracellular vesicles, exosomes, secretome, conditioned medium) in the process of normal and diabetic wound healing. The search strategy and inclusion criteria for the review were designed in accordance with PRISMA 2020 guidelines and were performed on PubMed/MEDLINE, Scopus, Web of Science, Embase, and ClinicalTrials.gov databases. Altogether, eleven eligible preclinical and clinical studies were included in a qualitative analysis. Because of the high level of heterogeneity in design, cell source, mode of administration, and outcomes, the meta-analysis could not be performed. All included studies revealed positive effects of MSC-based treatment on wound closure, angiogenesis, granulation tissue formation, collagen production, oxidative stress decrease, and pro-inflammatory macrophage polarisation modulation. MSC-derived cell-free therapy, especially exosomes and secretome, replicated the reparative effects of their parent cells and provided additional benefits like decreased immunogenicity, enhanced biosafety and ease of manufacturing. In addition, cell retention and sustained effect of therapeutic delivery were achieved through biomaterial-based systems such as hydrogels, nanofibers, injectable systems, and smart dressings. Even though the initial results from the clinical trials suggest promising safety and efficacy in chronic wound healing, there are several hurdles to be overcome, such as standardisation, manufacturing, regulatory approval, and clinical validation. Nevertheless, MSC and cell-free therapies seem to hold great potential in wound repair, especially in diabetic foot ulcers, and require further testing in RCTs before clinical use

Keywords : Mesenchymal Stem Cells, Wound Healing, Diabetic Foot Ulcer, Exosomes, Extracellular Vesicles, Regenerative Medicine, Cell-Free Therapy.

Paper Submission Last Date
31 - July - 2026

SUBMIT YOUR PAPER CALL FOR PAPERS
Video Explanation for Published paper

Never miss an update from Papermashup

Get notified about the latest tutorials and downloads.

Subscribe by Email

Get alerts directly into your inbox after each post and stay updated.
Subscribe
OR

Subscribe by RSS

Add our RSS to your feedreader to get regular updates from us.
Subscribe