Sebzda E, Mariathasan S, Ohteki T, Jones R, Bachmann M F, Ohashi P S
Ontario Cancer Institute, Toronto, Canada.
Annu Rev Immunol. 1999;17:829-74. doi: 10.1146/annurev.immunol.17.1.829.
Advances in gene technology have allowed the manipulation of molecular interactions that shape the T cell repertoire. Although recognized as fundamental aspects of T lymphocyte development, only recently have the mechanisms governing positive and negative selection been examined at a molecular level. Positive selection refers to the active process of rescuing MHC-restricted thymocytes from programmed cell death. Negative selection refers to the deletion or inactivation of potentially autoreactive thymocytes. This review focuses on interactions during thymocyte maturation that define the T cell repertoire, with an emphasis placed on current literature within this field.
基因技术的进步使得对塑造T细胞库的分子相互作用进行操控成为可能。尽管正负选择被认为是T淋巴细胞发育的基本方面,但直到最近才在分子水平上对其调控机制进行研究。阳性选择是指将受MHC限制的胸腺细胞从程序性细胞死亡中拯救出来的主动过程。阴性选择是指潜在的自身反应性胸腺细胞的缺失或失活。本综述着重于胸腺细胞成熟过程中决定T细胞库的相互作用,并重点关注该领域的当前文献。