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

Author:

Tanaka Rica123ORCID,Fujimura Satoshi13,Kado Makiko2,Fukuta Taro2,Arita Kayo13,Hirano-Ito Rie14,Mita Tomoya5,Watada Hirotaka5ORCID,Kato Yoshiteru6,Miyauchi Katsumi6,Mizuno Hiroshi23

Affiliation:

1. Division of Regenerative Therapy, Juntendo University Graduate School of Medicine, Tokyo, Japan

2. Department of Plastic and Reconstructive Surgery, Juntendo University School of Medicine, Tokyo, Japan

3. Intractable Disease Research Center, Juntendo University Graduate School of Medicine, Tokyo, Japan

4. Center for Genomic and Regenerative Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan

5. Department of Metabolism and Endocrinology, Juntendo University Graduate School of Medicine, Tokyo, Japan

6. Department of Internal Medicine, Division of Cardiology, Juntendo University School of Medicine, Tokyo, Japan

Abstract

Abstract 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 × 107 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.

Funder

Juntendo University

Japan Agency for Medical Research and Development

Ministry of Education, Culture, Sports, Science and Technology

Ministry of Health, Labour and Welfare

National Institutes of Biomedical Innovation, Health and Nutrition

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,General Medicine

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