Noble A
Department of Immunology, Guy's, King's & St Thomas' School of Medicine, London, UK.
Immunology. 2000 Nov;101(3):289-99. doi: 10.1046/j.1365-2567.2000.00133.x.
Rearrangement of gene segments occurs in T lymphocytes during thymic development as the T-cell receptor (TCR) is first expressed, allowing T cells to become central regulators of antigen specificity in the acquired immune system. However, further development of T cells occurs after population of peripheral lymphoid tissues, which can result in T-cell expansion and differentiation into effectors of various immune function, or progression to memory T cells, anergic cells or death by apoptosis. This review focuses on more recent developments concerning the choices that peripheral T cells make between first encountering antigen through TCR recognition and death. These decisions are associated with a process of genetic reprogramming that alters the behaviour of cells so that immune responses are appropriately regulated.
在胸腺发育过程中,基因片段重排发生于T淋巴细胞,此时T细胞受体(TCR)首次表达,使T细胞成为获得性免疫系统中抗原特异性的核心调节因子。然而,T细胞在外周淋巴组织定植后会进一步发育,这可能导致T细胞扩增并分化为具有各种免疫功能的效应细胞,或者发展为记忆T细胞、无反应性细胞或通过凋亡死亡。本综述聚焦于外周T细胞在通过TCR识别首次接触抗原与死亡之间所做选择的最新进展。这些决定与一个基因重编程过程相关,该过程会改变细胞行为,从而使免疫反应得到适当调节。