4.6 Article

Phase I/IIa Feasibility Trial of Autologous Quality- and quantity-Cultured Peripheral Blood Mononuclear Cell Therapy for Non-Healing Extremity Ulcers

期刊

STEM CELLS TRANSLATIONAL MEDICINE
卷 11, 期 2, 页码 146-158

出版社

OXFORD UNIV PRESS
DOI: 10.1093/stcltm/szab018

关键词

autologous stem cell transplantation; peripheral blood stem cell; vascular development; clinical trial

资金

  1. Juntendo University Intractable Disease Research Center
  2. Japan Agency for Medical Research and Development (AMED) [LS113]
  3. Strategic Research Foundation Grant-aided Project for Private Universities from the Ministry of Education, Culture, Sports, Science and Technology, Japan (MEXT) [S1411007]
  4. Japanese Ministry of Health, Labor, and Welfare [26713051, 22791737, 19H0381]
  5. National Institutes of Biomedical Innovation, Health, and Nutrition Regenerative Medicine Development Support Program
  6. Grants-in-Aid for Scientific Research [26713051, 22791737] Funding Source: KAKEN

向作者/读者索取更多资源

MNC-QQ therapy shows promising efficacy in chronic non-healing ischemic extremity wounds, improving vascular and skin perfusion and reducing pain intensity. It is also safe for patients.
Non-healing wounds are among the main causes of morbidity and mortality. We recently described a novel, serum-free ex vivo expansion system, the quantity and quality culture system (QQc), which uses peripheral blood mononuclear cells (PBMNCs) for effective and noninvasive regeneration of tissue and vasculature in murine and porcine models. In this prospective clinical study, we investigated the safety and efficacy of QQ-cultured peripheral blood mononuclear cell (MNC-QQ) therapy for chronic non-healing ischemic extremity wounds. Peripheral blood was collected from 9 patients with 10 chronic (>1 month) non-healing wounds (8 males, 1 female; 64-74 years) corresponding to ischemic extremity ulcers. PBMNCs were isolated and cultured using QQc. Within a 20-cm area surrounding the ulcer, 2 x 10(7) cells were injected under local anesthesia. Wound healing was monitored photometrically every 2 weeks. The primary endpoint was safety, whereas the secondary endpoint was efficacy at 12-week post-injection. All patients remained ambulant, and no deaths, other serious adverse events, or major amputations were observed for 12 weeks after cell transplantation. Six of the 10 cases showed complete wound closure with an average wound closure rate of 73.2% +/- 40.1% at 12 weeks. MNC-QQ therapy increased vascular perfusion, skin perfusion pressure, and decreased pain intensity in all patients. These results indicate the feasibility and safety of MNC-QQ therapy in patients with chronic non-healing ischemic extremity wounds. As the therapy involves transplanting highly vasculogenic cells obtained from a small blood sample, it may be an effective and highly vasculogenic strategy for limb salvage.

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