David Escors, Christopher Bricogne, Frederick Arce, Grazyna Kochan, Katarzyna Karwacz
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引用次数: 0
摘要
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。
On the Mechanism of T cell receptor down-modulation and its physiological significance.
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.