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作 者:王慧[1] 杨能[3] 周佩军[2] 邵琨[2] 赵菊平[2] 徐达[2] 王祥慧[2] 沈周俊[2] 路丽明[3] 刘世雄[1]
机构地区:[1]浙江省台州市中心医院泌尿外科,318000 [2]上海交通大学医学院附属瑞金医院泌尿外科 [3]上海市免疫学研究所
出 处:《中华器官移植杂志》2009年第10期604-607,共4页Chinese Journal of Organ Transplantation
基 金:国家自然科学基金(30571767)
摘 要:目的将供、受者骨髓细胞经混合培养后过继回输,以观察其对同种异体移植心脏存活时间和受者免疫功能的影响。方法取Balb/c小鼠和C57BL/6J小鼠的骨髓细胞,进行混合培养。配制含Balb/c小鼠和C57BL/6J小鼠脾淋巴细胞的混合淋巴细胞反应体系(MLR)以及含Balb/c小鼠和C3H小鼠脾淋巴细胞的MLR,分别加入混合培养的骨髓细胞,观察其对MLR中细胞增殖的影响。以C57BL/6J小鼠为供者,Balb/c小鼠为受者行腹腔异位心脏移植,实验分为4组:(1)移植对照组,受者仅进行心脏移植,不作其他处理;(2)实验对照组,心脏移植后给予西罗莫司灌胃;(3)实验组,移植手术结束前注射混合培养的骨髓细胞1×10^7个,术后给予西罗莫司;(4)第三方对照纽,受者接受C3H小鼠的移植心脏,手术结束前注射混合培养的骨髓细胞1×10^7个,术后给予西罗莫司。记录移植心脏存活时间;移植心脏停跳当日,取受者外周血,检测CD4^+CD25^+T淋巴细胞的比例及供者来源的H-2K“细胞的比例。结果加入混合培养的骨髓细胞后,Balb/c和C57BL/6J的MLR的淋巴细胞增殖率低于Balb/c和C3H的MLR。实验组移植心脏的存活时间长于其他3组(P〈0.05)。实验组CD4^+CD25^+T淋巴细胞的百分率高于其他3组(P〈0.05)。实验组外周血中H2K^6细胞的比例高于其他3组(P〈0.05)。结论受者输注混合培养的供、受者骨髓细胞可在一定程度上调节免疫应答,延长小鼠移植心脏的存活时间,该作用具有供者抗原特异性。Objective To investigate the effects of adoptive transfer of mix-cultured bone marrow ceils (BMC) from donor and recipient on allograft and immune system after the recipients preconditioned by a non-myeloablative regimen. Methods Mix-cultured BMC were added into mixed lymphocyte reaction. The effects of mix-cultured BMC on lymphocyte proliferation and their specificity were observed. Heart from C57BL/6 mouse was transplanted into Balb/c abdominal cavity, and the BMC from donor and recipient was mix-cultured and adoptively transferred. The recipients were divided as follows:Ⅰ, no treatment;Ⅱ, total body irradiation (TBI) + rapamune; Ⅲ, TBI + rapamune + mix-cultured BMC; Ⅳ, treated by the same protocol as group Ⅲ except that C3H mouse served as the donor. The survival of cardiac allograft in all groups was observed. The percentage of CD4+ CD25 + T and donor-derived H-2Kb ceils in peripheral blood of the recipient was measured by using FCM, when the allograft stopped heating. Results Mi^cultured BMC specifically down-regulated lymphocyte reaction in vitro. Adoptive transfer of mix-cultured BMC significantly prolonged the allograft survival in group Ⅲ, but not in group Ⅳ. And in recipient peripheral blood of group Ⅲ, the percentage of CD4+ CD25+ T cells and H-2K^6 cells was increased significantly. Specially, these effects were all acted as a donor antigen-specific manner. Conclusion Mix-cultured BMC can regulate immune response and prolong the cardiac allograft survival in a donor antigen-specific manner.
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