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主要组织相容性复合体 II 类分子在自身免疫中的呈递。

MHC Class II Presentation in Autoimmunity.

机构信息

Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry RAS, 117997 Moscow, Russia.

Department of Biological Chemistry, Evdokimov Moscow State University of Medicine and Dentistry, 127473 Moscow, Russia.

出版信息

Cells. 2023 Jan 14;12(2):314. doi: 10.3390/cells12020314.

DOI:10.3390/cells12020314
PMID:36672249
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9856717/
Abstract

Antigen presentation by major histocompatibility complex class II (MHC-II) molecules is crucial for eliciting an efficient immune response by CD4 T cells and maintaining self-antigen tolerance. Some MHC-II alleles are known to be positively or negatively associated with the risk of the development of different autoimmune diseases (ADs), including those characterized by the emergence of autoreactive T cells. Apparently, the MHC-II presentation of self-antigens contributes to the autoimmune T cell response, initiated through a breakdown of central tolerance to self-antigens in the thymus. The appearance of autoreactive T cell might be the result of (i) the unusual interaction between T cell receptors (TCRs) and self-antigens presented on MHC-II; (ii) the posttranslational modifications (PTMs) of self-antigens; (iii) direct loading of the self-antigen to classical MHC-II without additional nonclassical MHC assistance; (iv) the proinflammatory environment effect on MHC-II expression and antigen presentation; and (v) molecular mimicry between foreign and self-antigens. The peculiarities of the processes involved in the MHC-II-mediated presentation may have crucial importance in the elucidation of the mechanisms of triggering and developing ADs as well as for clarification on the protective effect of MHC-II alleles that are negatively associated with ADs.

摘要

主要组织相容性复合体 II 类 (MHC-II) 分子的抗原呈递对于 CD4 T 细胞引发有效的免疫反应和维持自身抗原耐受至关重要。一些 MHC-II 等位基因被认为与不同自身免疫性疾病 (AD) 的发病风险呈正相关或负相关,包括那些以自身反应性 T 细胞出现为特征的疾病。显然,MHC-II 对自身抗原的呈递有助于自身免疫性 T 细胞反应,该反应是通过在胸腺中对自身抗原的中枢耐受破坏而引发的。自身反应性 T 细胞的出现可能是由于 (i)T 细胞受体 (TCR) 与 MHC-II 上呈递的自身抗原之间的异常相互作用;(ii) 自身抗原的翻译后修饰 (PTMs);(iii) 自身抗原未经非经典 MHC 辅助直接加载到经典 MHC-II 上;(iv) 炎症环境对 MHC-II 表达和抗原呈递的影响;以及 (v) 外来和自身抗原之间的分子模拟。MHC-II 介导的呈递过程中涉及的这些过程的特殊性对于阐明触发和发展 AD 的机制以及澄清与 AD 呈负相关的 MHC-II 等位基因的保护作用具有至关重要的意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0003/9856717/a1624d094cec/cells-12-00314-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0003/9856717/97ab6e399e75/cells-12-00314-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0003/9856717/38f6ce468c6b/cells-12-00314-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0003/9856717/1646d2fc023f/cells-12-00314-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0003/9856717/47dece5b9547/cells-12-00314-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0003/9856717/1ae041891bdb/cells-12-00314-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0003/9856717/808ff6c7c8b4/cells-12-00314-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0003/9856717/a1624d094cec/cells-12-00314-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0003/9856717/97ab6e399e75/cells-12-00314-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0003/9856717/38f6ce468c6b/cells-12-00314-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0003/9856717/1646d2fc023f/cells-12-00314-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0003/9856717/47dece5b9547/cells-12-00314-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0003/9856717/1ae041891bdb/cells-12-00314-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0003/9856717/808ff6c7c8b4/cells-12-00314-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0003/9856717/a1624d094cec/cells-12-00314-g007.jpg

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