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T细胞激活信号是源自抗原呈递细胞还是效应辅助性T细胞?

Does the signal for the activation of T cells originate from the antigen-presenting cell or the effector T-helper?

作者信息

Cohn Melvin

机构信息

Conceptual Immunology Group, The Salk Institute for Biological Studies, 10010 North Torrey Pines Road, La Jolla, CA 92037, USA.

出版信息

Cell Immunol. 2006 May;241(1):1-6. doi: 10.1016/j.cellimm.2006.07.010. Epub 2006 Sep 11.

Abstract

The present view is that the antigen-presenting cell (APC) processes and presents simultaneously on its surface several different antigens that are displayed randomly (with respect to their being Self or Nonself) as peptide-MHC complexes. The naive T-cell interacting with its ligand on the APC is activated by "co-stimulation," the first step on the pathway to effectors. This view ignores the requirement for associative recognition of antigen (ARA) in mediating both the Self-Nonself discrimination and the regulation of effector class. The introduction of ARA as a requirement for these two decision functions highlights a critical role for the effector T-helper (eTh) and necessitates rethinking the contribution of the APC.

摘要

目前的观点认为,抗原呈递细胞(APC)处理并同时在其表面呈递几种不同的抗原,这些抗原作为肽-MHC复合物随机展示(相对于其为自身或非自身)。与APC上其配体相互作用的初始T细胞通过“共刺激”被激活,这是通向效应器途径的第一步。这种观点忽略了在介导自身-非自身区分和效应器类别调节中对抗原的关联识别(ARA)的要求。引入ARA作为这两种决策功能的要求,突出了效应性辅助性T细胞(eTh)的关键作用,并需要重新思考APC的作用。

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