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调节性T细胞在外周移植耐受的诱导与维持中作用

Regulatory T cells in the induction and maintenance of peripheral transplantation tolerance.

作者信息

Cobbold Stephen P, Graca Luis, Lin Chun-Yen, Adams Elizabeth, Waldmann Herman

机构信息

Sir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford, Oxfordshire, OX1 3RE, UK.

出版信息

Transpl Int. 2003 Feb;16(2):66-75. doi: 10.1007/s00147-003-0545-y. Epub 2003 Feb 4.

Abstract

It is now possible to induce donor-specific transplantation tolerance in adult rodents using non-depleting monoclonal antibodies against T cell co-receptor and co-stimulation molecules or by immunisation with tolerogenic antigen-presenting cells. It is a common finding of all these models of peripheral tolerance, as well as of various mouse models of autoimmune disease, that regulatory CD4(+) T cells are the principal mediators. There are currently no specific markers for regulatory T cells, but in some autoimmune models their activity has been associated with the expression of activation markers such as CD25 and CTLA4, or anti-inflammatory cytokines such as IL-10 and TGF-beta. CD4(+)CD25(+) T cells from both naïve and tolerised donors are able to transfer tolerance to grafts in lymphopenic recipients, and this may be directly applicable to bone-marrow transplantation. The challenge is now to understand the biological principles that allow such immune re-programming so that they can be safely applied to clinical organ grafting.

摘要

现在,使用针对T细胞共受体和共刺激分子的非耗竭性单克隆抗体,或通过用耐受性抗原呈递细胞进行免疫,在成年啮齿动物中诱导供体特异性移植耐受已成为可能。在所有这些外周耐受模型以及各种自身免疫性疾病小鼠模型中,一个共同的发现是调节性CD4(+) T细胞是主要的介导者。目前还没有调节性T细胞的特异性标志物,但在一些自身免疫模型中,它们的活性与激活标志物如CD25和CTLA4的表达,或抗炎细胞因子如IL-10和TGF-β的表达有关。来自未致敏和耐受供体的CD4(+)CD25(+) T细胞都能够将耐受性转移给淋巴细胞减少的受体中的移植物,这可能直接适用于骨髓移植。现在面临的挑战是了解允许这种免疫重编程的生物学原理,以便能够安全地应用于临床器官移植。

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