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作 者:解百宜[1] 陈继冰[2] 夏俊杰[1] 王永志[1] 梁华[3] 齐忠权[1]
机构地区:[1]厦门大学器官移植研究所,厦门361005 [2]厦门大学医学院基础医学部 [3]厦门大学附属中山医院心脏外科
出 处:《中华细胞与干细胞移植(电子版)》2009年第2期23-27,共5页
摘 要:目的探索联合应用共刺激通路阻断剂诱导记忆性心脏移植耐受的方法。方法皮肤预致敏小鼠,过继转移同种反应性记忆性T细胞(Tm),构建小鼠同种异体心脏移植模型后再联合阻断效应及记忆性T细胞激活途径,观察移植物生存期的改变,并从移植物和模型鼠两个角度探讨其可能的作用机制。结果①未处理小鼠脾脏中Tm占6.52﹪,而预致敏小鼠脾脏中Tm占26.5﹪;②平均存活时间为对照组5.17d,联合应用CTLA4Ig和anti-CD40L(二联用药)组10.33d,再联合应用anti-LFA-1和anti-OX40L(四联用药)组均〉100d;③移植物排斥对照组均为4级,二联用药组3B级,四联用药组为0级;④只有对照组脾脏物中CD44高表达;⑤对照组与二联用药组脾细胞增殖程度明显高于四联用药组;⑥治疗组的移植物中IL-2、IFN-γ和Foxp3基因的表达量明显低于对照组,并且四联用药组IL-10基因表达量明显升高。结论对于记忆性心脏移植模型,只有联合阻断效应和记忆性T细胞才可获得移植物长期耐受,其机制可能是明显降低移植物和移植受者细胞免疫应答水平的同时,诱导移植物中表达大量IL-10分泌性Tr1细胞。Objective The present study was undertaken to induce the tolerance of cardiac allografts in mice by combined costimulatory blockade after receving alloreactive memory T cell adoptive transfer. Methods Before the surgery,alloreactive memory T cells (Tm) from alloantigen-primed mice were adoptively transferred to the mice recipients of heterotopic cardiac transplantion. After the transplant,we treated the mice with combined costimulatory blockade to inhibit the activation of both effect and memory T cells. Furthermore,we studied the effects by comparing the mean survival time (MST) of the cardiac grafts and the possible mechanisms were evaluated. Results ① The percentage of memory T cells was 6.52﹪ in naive mice vs 26.5﹪ in alloantigen-primed mice; ② The MST was 5.17 days in the untreated group (Group A),and 10.33days in the group receiving CTLA4Ig and anti-CD40L treatment (Group B). For mice in Group C given CTLA4Ig,anti-CD40L,anti-LFA-1 and anti-OX40L MST was over 100 days; ③ In the histological tests,the mean scales were 4,3B and 0 for the above 3 groups respectively; ④ Only in the untreated group,we could find CD44high T cells; ⑤ The OD values of mixed lymphocyte reaction(MLR) were over 0.6 for both Group A and B,and less than 0.4 for Group C; ⑥ The gene expression levels of IL-2,IFN-γ and Foxp3 were lowerest in Group C,followed by Group B and A. In contrast,the expression levels of IL-10 were highest in Group C. Conclusions Inhibiting both effect and memory T cells could induce the tolerance of cardiac grafts and prevent the allografts from T cell infiltration. The mechanisms might be that the treatment promotes the functions of IL-10 producing CD4+ type 1 regulatory T (Tr1) cells,while suppresses the cellular immunity of the recipients.
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