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调节性 T 细胞在跨越主要组织相容性复合物屏障的 ESC 衍生组织移植接受中的作用。

A role for regulatory T cells in acceptance of ESC-derived tissues transplanted across an major histocompatibility complex barrier.

机构信息

Sir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford, United Kingdom.

出版信息

Stem Cells. 2010 Oct;28(10):1905-14. doi: 10.1002/stem.506.

Abstract

We have previously reported that ESC-derived tissues are subject to some level of immune privilege, which might facilitate induction of immune tolerance. Herein, we further demonstrate that fully allogeneic ESC-derived tissues are accepted with a regimen of coreceptor blockade even in recipients known to be relatively resistant to such a tolerizing protocol. Moreover, ESC-derived tissues could be spontaneously accepted across a class I major histocompatibility complex disparity. We further show that CD4(+)FoxP3(+) regulatory T cells (Treg) appear to be essential for this natural "privileged" state as their ablation with an anti-CD25 mAb results in rejection of ESC-derived tissue. This same treatment exposes activation of macrophages and effector CD8(+) T cells, suggesting that these cells are subject to regulatory T cell control. Thus, spontaneous acceptance of ESC-derived tissues mimics the acquired immune privilege induced by coreceptor blockade and is determined by Treg-mediated suppression.

摘要

我们之前曾报道过,ESC 衍生组织存在一定程度的免疫豁免,这可能有助于诱导免疫耐受。在此,我们进一步证明,即使在对这种耐受方案相对耐药的受者中,通过共受体阻断方案也可接受完全同种异体 ESC 衍生组织。此外,ESC 衍生组织可以在 I 类主要组织相容性复合物差异的情况下自发被接受。我们进一步表明,CD4(+)FoxP3(+)调节性 T 细胞(Treg)似乎是这种天然“特权”状态所必需的,因为用抗 CD25 mAb 消除它们会导致 ESC 衍生组织的排斥。这种相同的治疗方法暴露出巨噬细胞和效应 CD8(+)T 细胞的激活,表明这些细胞受到调节性 T 细胞的控制。因此,ESC 衍生组织的自发接受类似于共受体阻断诱导的获得性免疫豁免,并且由 Treg 介导的抑制决定。

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