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CD4+ CD25+ 调节性T细胞抑制自身抗体反应的成熟,但不抑制其起始。

CD4+ CD25+ regulatory T cells inhibit the maturation but not the initiation of an autoantibody response.

作者信息

Fields Michele L, Hondowicz Brian D, Metzgar Michele H, Nish Simone A, Wharton Gina N, Picca Cristina C, Caton Andrew J, Erikson Jan

机构信息

The Wistar Institute, Philadelphia, PA 19104, USA.

出版信息

J Immunol. 2005 Oct 1;175(7):4255-64. doi: 10.4049/jimmunol.175.7.4255.

Abstract

To investigate the mechanism by which T regulatory (Treg) cells may control the early onset of autoimmunity, we have used an adoptive transfer model to track Treg, Th, and anti-chromatin B cell interactions in vivo. We show that anti-chromatin B cells secrete Abs by day 8 in vivo upon provision of undeviated, Th1- or Th2-type CD4+ T cell help, but this secretion is blocked by the coinjection of CD4+ CD25+ Treg cells. Although Treg cells do not interfere with the initial follicular entry or activation of Th or B cells at day 3, ICOS levels on Th cells are decreased. Furthermore, Treg cells must be administered during the initial phases of the Ab response to exert full suppression of autoantibody production. These studies indicate that CD25+ Treg cells act to inhibit the maturation, rather than the initiation, of autoantibody responses.

摘要

为了研究调节性T(Treg)细胞控制自身免疫早期发作的机制,我们使用了过继转移模型在体内追踪Treg、Th和抗染色质B细胞的相互作用。我们发现,在提供未偏离的、Th1或Th2型CD4+ T细胞辅助的情况下,抗染色质B细胞在体内第8天分泌抗体,但这种分泌被共注射CD4+ CD25+ Treg细胞所阻断。虽然Treg细胞在第3天不干扰Th或B细胞最初进入滤泡或激活,但Th细胞上的ICOS水平会降低。此外,Treg细胞必须在抗体应答的初始阶段给药,才能充分抑制自身抗体的产生。这些研究表明,CD25+ Treg细胞的作用是抑制自身抗体应答的成熟,而非起始。

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