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外周 T 细胞再进入胸腺并干扰中枢耐受诱导。

Peripheral T cells re-enter the thymus and interfere with central tolerance induction.

机构信息

Institute for Immunology, Ludwig-Maximilians-University, D-80336 Munich, Germany.

出版信息

J Immunol. 2011 May 15;186(10):5612-9. doi: 10.4049/jimmunol.1004010. Epub 2011 Apr 6.

Abstract

The thymus mainly contains developing thymocytes that undergo thymic selection. In addition, some mature activated peripheral T cells can re-enter the thymus. We demonstrated in this study that adoptively transferred syngeneic Ag-specific T cells can enter the thymus of lymphopenic mice, where they delete thymic dendritic cells and medullary thymic epithelial cells in an Ag-specific fashion, without altering general thymic functions. This induced sustained thymic release of autoreactive self-Ag-specific T cells suggested that adoptively transferred activated T cells can specifically alter the endogenous T cell repertoire by erasing negative selection of their own specificities. Especially in clinical settings in which adoptively transferred T cells cause graft-versus-host disease or graft-versus-leukemia, as well as in adoptive tumor therapies, these findings might be of importance, because the endogenous T cell repertoire might be skewed to contribute to both manifestations.

摘要

胸腺主要包含正在经历胸腺选择的发育中的胸腺细胞。此外,一些成熟的激活外周 T 细胞可以重新进入胸腺。我们在这项研究中证明,过继转移的同种抗原特异性 T 细胞可以进入淋巴缺失小鼠的胸腺,在那里它们以抗原特异性的方式删除胸腺树突状细胞和髓质胸腺上皮细胞,而不改变一般的胸腺功能。这种诱导的持续的胸腺释放自身反应性的自身抗原特异性 T 细胞表明,过继转移的激活 T 细胞可以通过消除自身特异性的负选择来特异性地改变内源性 T 细胞库。特别是在过继转移 T 细胞引起移植物抗宿主病或移植物抗白血病的临床环境中,以及在过继性肿瘤治疗中,这些发现可能很重要,因为内源性 T 细胞库可能会偏向于导致这两种表现。

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