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五幕论 MHC 限制与 T 细胞识别

A Disquisition on MHC Restriction and T Cell Recognition in Five Acts.

机构信息

Department of Pathology, Case Western Reserve University, Cleveland, Ohio.

出版信息

Viral Immunol. 2020 Apr;33(3):153-159. doi: 10.1089/vim.2019.0182.

Abstract

The seminal discovery in the early 1970s, credited to Peter Doherty and Rolf Zinkernagel, of major histocompatibility complex (MHC) restriction exhibited by cytotoxic T cells represented a major conceptual advance in understanding antigen recognition by conventional T cells. This advance also led to other major new insights into the ontogeny and immunobiology of T cells and catalyzed a renaissance in viral immunology. In this commentary in honor of Peter Doherty, I offer five brief reflections on different aspects of the phenomenon of MHC restriction and the process by which it was discovered and explained. In the first of these sections, I offer a reinterpretation of MHC restriction that reframes the constraints on self-MHC recognition in terms of the probabilities of recognizing a given nominal antigen peptide in the context of an MHC molecule that is nonself on the basis of differing in amino acid sequence from the self-restriction element at one or more positions. Subsequent sections address: (i) the ways in which general ideas, developed subsequent to the discovery of MHC restriction, about the intricacies of antigen recognition by antibodies apply to T cell receptors binding to MHC/peptide complexes; (ii) how to reconcile the existence of MHC restriction with the impressive magnitude of T cell responses to nonself MHC antigens; (iii) the possible relevance to MHC restriction and immune system function of ideas from mathematical logic that relate to the consequences of self-reference; and (iv) the implications for the philosophy of science of MHC restriction and the processes of its discovery and acceptance within the immunology research community.

摘要

20 世纪 70 年代初,彼得·多尔蒂(Peter Doherty)和罗尔夫·津克纳格尔(Rolf Zinkernagel)的开创性发现表明,细胞毒性 T 细胞具有主要组织相容性复合体(MHC)限制,这是理解常规 T 细胞识别抗原的重大概念性进展。这一进展还导致了对 T 细胞发生和免疫生物学的其他重大新见解,并推动了病毒免疫学的复兴。在这篇纪念彼得·多尔蒂的评论中,我就 MHC 限制现象及其发现和解释过程的五个不同方面进行了简要的思考。在这些内容中的第一个部分,我对 MHC 限制进行了重新解释,从基于氨基酸序列差异的角度,重新构建了对自我 MHC 识别的限制,将其表述为在基于氨基酸序列差异的情况下,识别给定的非自身 MHC 分子背景下的特定名义抗原肽的概率。后续的部分将分别讨论以下内容:(i)在 MHC 限制发现之后发展起来的关于抗体识别抗原复杂性的一般思想,如何适用于与 MHC/肽复合物结合的 T 细胞受体;(ii)如何调和 MHC 限制的存在与 T 细胞对非自身 MHC 抗原的巨大反应之间的矛盾;(iii)来自数理逻辑的与自我参照的后果相关的思想可能与 MHC 限制和免疫系统功能有关;(iv)MHC 限制及其在免疫学研究界的发现和接受过程对科学哲学的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8cd/7185361/959f9a7fb7e1/vim.2019.0182_figure1.jpg

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