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通过T细胞疫苗接种延长大鼠心脏同种异体移植的存活时间。

Prolongation of survival of rat cardiac allografts by T cell vaccination.

作者信息

Shapira O M, Mor E, Reshef T, Pfeffermann R A, Cohen I R

机构信息

Department of Cell Biology, Weizmann Institute of Science, Rehovot, Israel.

出版信息

J Clin Invest. 1993 Feb;91(2):388-90. doi: 10.1172/JCI116211.

DOI:10.1172/JCI116211
PMID:8432846
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC287935/
Abstract

Administration of attenuated, activated autoimmune T lymphocytes to syngeneic mice and rats has been shown to prevent or induce remission of experimental autoimmune diseases specific for the autoimmune T cells. The process has been termed "T cell vaccination." In a recent study, T cell vaccination was done using T cells sensitized to rat alloantigens. The procedure produced a significant reduction of the mixed lymphocyte reaction (MLR) against allogeneic cells. The reduction in MLR was not specific: Vaccination with T cells specific for stimulator cells of one allotype led to a reduced MLR stimulated by cells of another allotype. The present study was undertaken to examine whether T cell vaccination can induce tolerance to transplantation antigens in vivo. We used the model of heterotopic cardiac transplantation in rats. We now report that vaccinating rats with syngeneic, activated, alloantigen-primed T lymphocytes significantly prolonged survival of rat cardiac allografts. The effect of T cell vaccination was most evident when the T cells had been obtained from rats specifically sensitized against the donor rats: Brown-Norway (BN) allografts in control Wistar rats survived 8.5 +/- 0.4 d while BN allografts survived 29.2 +/- 7.1 d in Wistar rats that had been vaccinated with Wistar anti-BN cells. Vaccination of Wistar rats with Wistar anti-hooded T cells prolonged survival of BN heart allografts to a lesser but significant degree (13.0 +/- 1.1 d). Thus, T cell vaccination of recipients can prolong survival of allografts.

摘要

已证明,将减毒、活化的自身免疫性T淋巴细胞接种于同基因小鼠和大鼠,可预防或诱导针对自身免疫性T细胞的实验性自身免疫疾病缓解。该过程被称为“T细胞疫苗接种”。在最近一项研究中,使用对大鼠同种异体抗原致敏的T细胞进行T细胞疫苗接种。该程序使针对同种异体细胞的混合淋巴细胞反应(MLR)显著降低。MLR的降低并非特异性的:用针对一种同种异型刺激细胞的特异性T细胞进行疫苗接种,会导致另一种同种异型细胞刺激的MLR降低。本研究旨在探讨T细胞疫苗接种是否能在体内诱导对移植抗原的耐受性。我们使用大鼠异位心脏移植模型。我们现在报告,用同基因、活化、经同种异体抗原致敏的T淋巴细胞对大鼠进行疫苗接种,可显著延长大鼠心脏异体移植的存活时间。当T细胞取自对供体大鼠特异性致敏的大鼠时,T细胞疫苗接种的效果最为明显:对照Wistar大鼠中的Brown-Norway(BN)异体移植存活8.5±0.4天,而在接种了Wistar抗BN细胞的Wistar大鼠中,BN异体移植存活29.2±7.1天。用Wistar抗带帽T细胞对Wistar大鼠进行疫苗接种,可使BN心脏异体移植的存活时间延长至较小但显著的程度(13.0±1.1天)。因此,对受体进行T细胞疫苗接种可延长异体移植的存活时间。

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引用本文的文献

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J Immunol. 2007 Sep 1;179(5):2731-40. doi: 10.4049/jimmunol.179.5.2731.

本文引用的文献

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Vaccination against autoimmune encephalomyelitis with T-lymphocyte line cells reactive against myelin basic protein.用针对髓鞘碱性蛋白的T淋巴细胞系细胞对自身免疫性脑脊髓炎进行疫苗接种。
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T lymphocyte line specific for thyroglobulin produces or vaccinates against autoimmune thyroiditis in mice.针对甲状腺球蛋白的T淋巴细胞系可在小鼠中引发自身免疫性甲状腺炎或用于预防自身免疫性甲状腺炎。
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