Messaoudi Ilhem, Guevara Patiño Jose A, Dyall Ruben, LeMaoult Joël, Nikolich-Zugich Janko
Vaccine and Gene Therapy Institute and the Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, OR 97006, USA.
Science. 2002 Nov 29;298(5599):1797-800. doi: 10.1126/science.1076064.
Major histocompatibility complex (mhc)-encoded molecules govern immune responses by presenting antigenic peptides to T cells. The extensive polymorphism of genes encoding these molecules is believed to enhance immune defense by broadening the array of antigenic peptides available for T cell recognition, but direct evidence supporting the importance of this mechanism in combating pathogens is limited. Here we link mhc polymorphism-driven diversification of the cytotoxic T lymphocyte (CTL) repertoire to the generation of high-avidity, protective antiviral T cells and to superior antiviral defense. Thus, much of the beneficial effect of the mhc polymorphism in immune defense may be due to its critical influence on the properties of the selected CTL repertoire.
主要组织相容性复合体(MHC)编码的分子通过将抗原肽呈递给T细胞来调控免疫反应。编码这些分子的基因具有广泛的多态性,人们认为这通过扩大可供T细胞识别的抗原肽种类来增强免疫防御,但支持该机制在对抗病原体中重要性的直接证据有限。在此,我们将MHC多态性驱动的细胞毒性T淋巴细胞(CTL)库多样化与高亲和力、保护性抗病毒T细胞的产生以及卓越的抗病毒防御联系起来。因此,MHC多态性在免疫防御中的许多有益作用可能归因于其对所选CTL库特性的关键影响。