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作 者:何凡[1] 陈知水[1] 徐胜元[1] 蔡明[1] 吴敏[1] 李红洲[1]
机构地区:[1]华中科技大学同济医学院附属同济医院器官移植研究所,卫生部/教育部重点实验室,湖北武汉430030
出 处:《武汉大学学报(医学版)》2009年第3期290-293,F0002,共5页Medical Journal of Wuhan University
基 金:湖北省科技攻关重大项目(编号:2006AA301A06)
摘 要:目的:探讨不同T细胞在门静脉输注诱导耐受中的作用。方法:门静脉输注经丝裂霉素处理过的C57小鼠脾细胞给BALB/c,7 d后分离受鼠脾细胞,流式分选其中CD3+、CD4+、CD8+T细胞,过继输注给另一BALB/c,并同时行C57或C3H来源的心脏移植,观察并比较心脏移植物存活时间。结果:过继输注PVI鼠T细胞后,可以转移耐受;过继输注PVI鼠CD4+T细胞,可使供体来源的C57供心存活时间延长,而对第三系C3H供心存活时间无明显延长。过继输注PVI鼠CD8+T细胞无此效应。结论:在门静脉输注诱导耐受的模型中,CD4+T细胞可以转移耐受,且此耐受为抗原特异性,CD8+T细胞无此效应。To analyze the role of different subsets of T lymphocytes in transferring tolerance induced by portal venous injection. Methods: C57BL/6 (B6) mice were used as donors. Seven days after portal venous injection of mitomycin-treated B6 splenocytes into BALB/c mice, the splenocytes of the recipient were isolate, and CD4+ and CDS+T lymphocytes were sorted by FACSAria. The sorted CD4+ (CD8+ ) T lymphocytes were then transfused into another BALB/c mice followed by heterotopic implantation of a B6 heart allograft. C3H heart allografts and normal BALB/c mice were used as controls. The rejection response and survival of the allograft were observed. Results: When transfusion with CD4+T tymphocytes isolated from BALB/c mice treated with a portal injection of B6 splenocytes, the subsequent transplanted B6 allograft survived longer than C3H allograft. Similar results were not observed in normal BALB/c or BALB/c mice with transfusion of CD8+T lymphocytes from BALB/c mice treated with a portal injection of B6 splenocytes. Conclusion: This finding indicates that CD4+T lymphocytes, rather than CD8+T lymphocytes, play an important role in transferring tolerance induced by portal venous injection and this tolerance is antigen-specific.
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