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前沿:滤泡归巢的诱导先于效应性 Th 细胞的发育。

Cutting edge: induction of follicular homing precedes effector Th cell development.

作者信息

Schaerli P, Loetscher P, Moser B

机构信息

Theodor-Kocher Institute, University of Bern, Bern, Switzerland.

出版信息

J Immunol. 2001 Dec 1;167(11):6082-6. doi: 10.4049/jimmunol.167.11.6082.

Abstract

Transition from naive to Ag-experienced effector/memory CD4+ T cells is initiated during contact with APC in secondary lymphoid tissue. Here, we demonstrate that the CXCR5 is a marker for recently activated memory CD4+ T cells. CXCR5 is rapidly induced during contact with Ag-presenting dendritic cells, well before T cell expansion and effector cell development, and is irreversibly lost on terminally differentiated effector cells. Furthermore, immunization of human volunteers with a recall Ag results in rapid accumulation of Ag-responsive, CXCR5-expressing CD4+ T cells in peripheral blood. Early acquisition of a new migration program enables T zone CD4+ T cells to develop into follicular B helper T cells or, alternatively, into circulating memory CD4+ T cells. Together, CXCR5 unequivocally defines pre-effector memory CD4+ T cells generated during ongoing immune responses.

摘要

从初始CD4⁺ T细胞向抗原经验丰富的效应/记忆CD4⁺ T细胞的转变在次级淋巴组织中与抗原呈递细胞接触期间启动。在此,我们证明CXCR5是最近活化的记忆CD4⁺ T细胞的标志物。在与抗原呈递树突状细胞接触期间,早在T细胞扩增和效应细胞发育之前,CXCR5就被迅速诱导,并且在终末分化的效应细胞上不可逆地丢失。此外,用回忆性抗原来免疫人类志愿者会导致外周血中抗原反应性、表达CXCR5的CD4⁺ T细胞迅速积累。早期获得新的迁移程序使T区CD4⁺ T细胞能够发育成滤泡辅助性B细胞,或者发育成循环记忆CD4⁺ T细胞。总之,CXCR5明确地定义了在正在进行的免疫反应过程中产生的前效应记忆CD4⁺ T细胞。

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