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MHC II类四聚体与抗原特异性T细胞的探寻:定义、偏离、清除

MHC Class II tetramers and the pursuit of antigen-specific T cells: define, deviate, delete.

作者信息

Mallone Roberto, Nepom Gerald T

机构信息

Benaroya Research Institute at Virginia Mason, Seattle, WA 98101, USA.

出版信息

Clin Immunol. 2004 Mar;110(3):232-42. doi: 10.1016/j.clim.2003.11.004.

Abstract

Selective expansion and activation of a very small number of antigen-specific CD4(+) T cells is a remarkable and essential property of the adaptive immune response. Antigen-specific T cells were until recently identified only indirectly by functional assays, such as antigen-induced cytokine secretion and proliferation. The advent of MHC Class II tetramers has added a pivotal tool to our research armamentarium, allowing the definition of allo- and autoimmune responses in deeper detail. Rare antigen-specific CD4(+) cells can now be selectively identified, isolated and characterized. The same tetramer reagents also provide a new mean of stimulating T cells, more closely reproducing the MHC-peptide/TCR interaction. This property allows the use of tetramers to direct T cells toward the more desirable outcome, that is, activation (in malignancies and infectious diseases) or Th2/T regulatory cell deviation, anergy and deletion (in autoimmune diseases). These experimental approaches hold promise for diagnostic, prognostic and therapeutic applications.

摘要

极少数抗原特异性CD4(+) T细胞的选择性扩增和激活是适应性免疫反应的显著且基本特性。直到最近,抗原特异性T细胞还只能通过功能检测(如抗原诱导的细胞因子分泌和增殖)间接鉴定。MHC II类四聚体的出现为我们的研究手段增添了关键工具,使我们能够更深入地定义同种异体和自身免疫反应。现在可以选择性地鉴定、分离和表征罕见的抗原特异性CD4(+) 细胞。同样的四聚体试剂还提供了一种刺激T细胞的新方法,能更精确地重现MHC-肽/TCR相互作用。这一特性使得可以利用四聚体引导T细胞实现更理想的结果,即激活(在恶性肿瘤和传染病中)或Th2/T调节性细胞偏向、无反应性和缺失(在自身免疫性疾病中)。这些实验方法在诊断、预后和治疗应用方面具有前景。

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