Department of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
J Immunol. 2012 Oct 15;189(8):3800-4. doi: 10.4049/jimmunol.1103080. Epub 2012 Sep 14.
Phagocyte NADPH oxidase plays a key role in pathogen clearance via reactive oxygen species (ROS) production. Defects in oxidase function result in chronic granulomatous disease with hallmark recurrent microbial infections and inflammation. The oxidase's role in the adaptive immune response is not well understood. Class II presentation of cytoplasmic and exogenous Ag to CD4(+) T cells was impaired in human B cells with reduced oxidase p40(phox) subunit expression. Naturally arising mutations, which compromise p40(phox) function in a chronic granulomatous disease patient, also perturbed class II Ag presentation and intracellular ROS production. Reconstitution of patient B cells with a wild-type, but not a mutant, p40(phox) allele restored exogenous Ag presentation and intracellular ROS generation. Remarkably, class II presentation of epitopes from membrane Ag was robust in p40(phox)-deficient B cells. These studies reveal a role for NADPH oxidase and p40(phox) in skewing epitope selection and T cell recognition of self Ag.
吞噬细胞 NADPH 氧化酶通过产生活性氧(ROS)在病原体清除中发挥关键作用。氧化酶功能缺陷会导致慢性肉芽肿病,其特征是反复发生微生物感染和炎症。氧化酶在适应性免疫反应中的作用尚不清楚。在人类 B 细胞中,氧化酶 p40(phox)亚基表达减少会损害细胞内和外源性 Ag 向 CD4(+)T 细胞的 II 类呈递。在慢性肉芽肿病患者中,影响 p40(phox)功能的天然发生突变也会干扰 II 类 Ag 呈递和细胞内 ROS 产生。用野生型而非突变型 p40(phox)等位基因重建患者的 B 细胞可恢复外源性 Ag 呈递和细胞内 ROS 的产生。值得注意的是,p40(phox)缺陷 B 细胞中膜 Ag 表位的 II 类呈递非常稳健。这些研究揭示了 NADPH 氧化酶和 p40(phox)在影响表位选择和 T 细胞识别自身 Ag 中的作用。