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[大鼠肝脏同种异体移植中浸润细胞的表型和功能分析]

[Phenotypic and functional analyses of cells infiltrating rat hepatic allograft].

作者信息

Osaka Y

机构信息

Second Department of Surgery, Kyoto Prefectural University of Medicine, Japan.

出版信息

Nihon Geka Gakkai Zasshi. 1993 Feb;94(2):147-54.

PMID:8464411
Abstract

In order to elucidate the immunological characteristics of rat liver transplantation, graft infiltrating cells (GIC) were isolated from rat hepatic allografts, and phenotypic and functional analyses were performed. Long-surviving combination (Lewis engrafted BN liver, MST = 166.8 +/- 28.1 days, n = 10) and acutely-rejected combination (Lewis engrafted DA liver, MST = 9.6 +/- 0.3 days, n = 6) were compared. Relative proportions of all T cells and activated T cells assessed by flow cytometry were significantly higher in Lewis recipients of acutely-rejected combination than in those of long-surviving combination on day 6 after transplantation. Phenotypic analyses of GIC on days 6, 14, and 45 after transplantation in Lewis hosts of long-surviving combination were assessed. All T cells, OX-8 positive cells (Tc/s, NK), and OX-39 positive (IL-2 receptor) cells showed peak levels on day 6 and decreased on day 45. Cytotoxic activity of GIC toward donor lymphocytes on day 6 was stronger in host of acutely-rejected combination (18.9 +/- 4.0%, E/T = 50) than in that of long-surviving combination (5.3 +/- 2.8%). On the other hand, NK activity in Lewis host of long-surviving combination was high (17.5 +/- 3.0%, E/T = 100) on day 6 after transplantation. These results demonstrate that some immunosuppressive mechanism is present already on day 6 after transplantation, and that infiltration or activation of cytotoxic T cells is inhibited in long-surviving combination of rat hepatic allografts.

摘要

为阐明大鼠肝移植的免疫学特征,从大鼠肝脏同种异体移植物中分离出移植物浸润细胞(GIC),并进行表型和功能分析。比较了长期存活组合(Lewis大鼠植入BN大鼠肝脏,中位生存时间[MST]=166.8±28.1天,n=10)和急性排斥组合(Lewis大鼠植入DA大鼠肝脏,MST=9.6±0.3天,n=6)。移植后第6天,通过流式细胞术评估的急性排斥组合的Lewis受体中所有T细胞和活化T细胞的相对比例显著高于长期存活组合的Lewis受体。评估了长期存活组合的Lewis宿主在移植后第6天、14天和45天GIC的表型分析。所有T细胞、OX-8阳性细胞(Tc/s、NK)和OX-39阳性(IL-2受体)细胞在第6天显示出峰值水平,并在第45天下降。急性排斥组合的宿主在第6天GIC对供体淋巴细胞的细胞毒性活性(18.9±4.0%,效靶比[E/T]=50)强于长期存活组合的宿主(5.3±2.8%)。另一方面,长期存活组合的Lewis宿主在移植后第6天NK活性较高(17.5±3.0%,E/T=100)。这些结果表明,在移植后第6天已经存在一些免疫抑制机制,并且在大鼠肝脏同种异体移植的长期存活组合中细胞毒性T细胞的浸润或活化受到抑制。

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