首页 | 本学科首页   官方微博 | 高级检索  
     


Anti-Donor Regulatory T-Cell Therapy in Adult-to-Adult Living Donor Liver Transplantation: A Case Report
Affiliation:1. Department of Surgery, Nagasaki University Graduate School of Biomedical Sciences/Nagasaki University Hospital, Nagasaki, Japan;2. Atopy (Allergy) Research Center, Juntendo University, Tokyo, Japan;3. Department of Gastroenterological Surgery I, Hokkaido University, Hokkaido. Japan;4. Transfusion and Cell Therapy Unit, Nagasaki University Hospital, Nagasaki, Japan;5. Research Institute, St. Mary''s Hospital, Fokuoka, Japan;1. Department of General Surgery, Faculty of Medicine, Erzincan Binali Yildirim University, Erzincan, Turkey;2. Department of Histology, Faculty of Medicine, Erzincan Binali Yildirim University, Erzincan, Turkey;3. Department of Pharmacology, Faculty of Medicine, Erzincan Binali Yildirim University, Erzincan, Turkey;4. Department of Biochemistry, Faculty of Pharmacy, Ibrahim Cecen University, Agri, Turkey;1. Division of Nephrology, Department of Medicine, Hamad Medical Corporation, Doha, Qatar;2. Weill Cornell Medical College, Doha, Qatar;3. Division of Transplantation Surgery, Department of Surgery, Hamad Medical Corporation, Doha, Qatar;1. Department of Nephrology, Institute of Kidney Diseases and Research Centre, Dr. H. L. Trivedi Institute of Transplantation Sciences, Ahmedabad, Gujarat, India;2. Department of Nephrology, Muljibhai Patel Urological Hospital, Nadiad, Gujarat, India;3. Department of Nephrology, Rabindranath Tagore International Institute of Cardiac Sciences, Kolkata, West Bengal;4. Department of Nephrology, Osmania General Hospital, Hyderabad, India;5. Department of Nephrology, Nizam''s Institute of Medical Sciences, Panjagutta, Hyderabad, India;6. Department of Nephrology, Institute of Post-Graduate Medical Education & Research, Kolkata, India;7. Department of Nephrology, Manipal Hospital, Bangalore, India;8. Department of Nephrology, Kovai Medical Centre and Hospital, Coimbatore, Tamil Nadu, India;9. Department of Nephrology, Jaslok Hospitals, Mumbai, India;10. Departmentt of Nephrology, Centre Yashoda Hospitals, Secunderabad, India;11. Department of Nephrology and Renal Transplantation, Indira Gandhi Institute of Medical Science, Patna, India;12. Lakeshore Hospital, Kochi, Kerala, India;13. B. J. Medical Hospital, Civil Hospital, Ahmedabad, Gujarat, India;14. Department of Gynecology, Institute of Kidney Diseases and Research Centre, Dr. H. L. Trivedi Institute of Transplantation Sciences, Ahmedabad, Gujarat, India;1. McGovern Medical School, University of Texas Health Science Center, Houston, Texas;2. Texas Children''s Hospital Department of Radiology, Interventional Radiology, Houston, Texas;3. Texas Children''s Hospital Department of Critical Care, and Liver Intensive Care Unit, Houston, Texas;4. Texas Children''s Hospital, Liver Transplantation Service, Houston, Texas;5. Baylor College of Medicine, Michael E. DeBakey Department of Surgery, Division of Abdominal Transplantation, Houston, Texas;1. Division of Abdominal Transplantation, Mayo Clinic, Phoenix, Arizona;2. Transplant Center, Mayo Clinic, Phoenix, Arizona;3. Laboratory Medicine and Pathology, Mayo Clinic, Phoenix, Arizona;4. Division of Infectious Diseases, Mayo Clinic, Phoenix, Arizona;1. Department of Organ Transplantation;2. Department of Pathology;3. Department of Cardiovascular Surgery, Changhai Hospital, Second Military Medical University, Shanghai, China
Abstract:
We report on the case of a 50-year-old female patient with symptomatic polycystic liver disease who underwent living donor liver transplantation (LDLT) using right liver graft from her ABO-identical husband. To achieve operational tolerance, regulatory T-cell (T-reg)–based cell therapy was applied, following the protocol introduced by Todo et al. Briefly, donor lymphocytes were collected by leukapheresis 20 days before LDLT without any adverse events, and the cells were irradiated with a dose of 30 Gy and kept frozen. Lymphopheresis of the recipient was conducted in a similar manner 1 day before LDLT, and donor cells and recipient cells were cultured with anti-CD80/86 antibodies to induce the donor-specific T-reg. At 14 days of culture, the CD4+CD25+Foxp3+ cells had increased from 1.51% to 5.21%, and mixed lymphocyte reaction assay using an intracellular fluorescent dye carboxyfluorescein diacetate succinimidyl ester-labeling technique revealed donor-specific hyporesponsiveness of CD4-positive lymphocytes. On postoperative day (POD) 13 (14 days of culture), these cells were infused to the recipient intravenously without any adverse events. Initial immunosuppression consisted of tacrolimus, steroid and mycophenolate mofetil (MMF), and cyclophosphamide (40 mg/kg) administered on POD 5. Both the steroid and MMF were continued until 4 weeks after LDLT, and the patient was discharged on POD 30 with normal liver function. On POD 52, the patient developed acute cellular rejection and received appropriate reinforcement of immunosuppressive therapy and is currently doing well with normal liver function 30 months after LDLT with reduced anti-donor allo-activity. In summary, T-reg therapy was safely performed in adult LDLT, and we are following the patient carefully to determine whether she can achieve operational tolerance in the future.
Keywords:
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号