David Escors, Christopher Bricogne, Frederick Arce, Grazyna Kochan, Katarzyna Karwacz
{"title":"On the Mechanism of T cell receptor down-modulation and its physiological significance.","authors":"David Escors, Christopher Bricogne, Frederick Arce, Grazyna Kochan, Katarzyna Karwacz","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Effective, long-lasting immune responses largely depend upon T cell reponses. Antigen-specific T lymphocytes are activated and differentiate into effector T cells after antigen presentation by professional antigen presenting cells (APCs). However, T cell responses are tightly regulated to prevent T cell hyperactivation which may end up in autoimmune pathology. One of these regulatory mechanisms is ligand-induced TCR down-modulation, a process by which TCRs are removed from the T cell surface shortly after engagement with their cognate antigenic peptide associated to MHC molecules on the APC. TCR down-modulation is a complicated process. Here we briefly describe the three main models that attempt to clarify this mechanism in the context of T cell activation and function.</p>","PeriodicalId":89629,"journal":{"name":"The journal of bioscience and medicine","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2011-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3272427/pdf/ukmss-36879.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The journal of bioscience and medicine","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Effective, long-lasting immune responses largely depend upon T cell reponses. Antigen-specific T lymphocytes are activated and differentiate into effector T cells after antigen presentation by professional antigen presenting cells (APCs). However, T cell responses are tightly regulated to prevent T cell hyperactivation which may end up in autoimmune pathology. One of these regulatory mechanisms is ligand-induced TCR down-modulation, a process by which TCRs are removed from the T cell surface shortly after engagement with their cognate antigenic peptide associated to MHC molecules on the APC. TCR down-modulation is a complicated process. Here we briefly describe the three main models that attempt to clarify this mechanism in the context of T cell activation and function.
有效、持久的免疫反应在很大程度上取决于 T 细胞的反应。抗原特异性 T 淋巴细胞在专业抗原呈递细胞(APC)呈递抗原后被激活并分化为效应 T 细胞。然而,T 细胞反应受到严格调控,以防止 T 细胞过度活化,最终导致自身免疫性病变。其中一种调节机制是配体诱导的 TCR 下调,TCR 在与 APC 上与 MHC 分子相关的同源抗原肽接触后不久就会从 T 细胞表面移除。TCR 下调是一个复杂的过程。在此,我们将简要介绍试图从 T 细胞活化和功能的角度阐明这一机制的三个主要模型。