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对病毒感染的中和抗体反应与非经典MHC II类基因H2-Ob相关。

Neutralizing Antibody Responses to Viral Infections Are Linked to the Non-classical MHC Class II Gene H2-Ob.

作者信息

Denzin Lisa K, Khan Aly A, Virdis Francesca, Wilks Jessica, Kane Melissa, Beilinson Helen A, Dikiy Stanislav, Case Laure K, Roopenian Derry, Witkowski Michele, Chervonsky Alexander V, Golovkina Tatyana V

机构信息

Child Health Institute of NJ, Department of Pediatrics, Rutgers Robert Wood Johnson Medical School, Rutgers, The State University of NJ, New Brunswick, NJ 08901, USA.

Toyota Technological Institute at Chicago, Chicago, IL 60637, USA.

出版信息

Immunity. 2017 Aug 15;47(2):310-322.e7. doi: 10.1016/j.immuni.2017.07.013.

Abstract

Select humans and animals control persistent viral infections via adaptive immune responses that include production of neutralizing antibodies. The precise genetic basis for the control remains enigmatic. Here, we report positional cloning of the gene responsible for production of retrovirus-neutralizing antibodies in mice of the I/LnJ strain. It encodes the beta subunit of the non-classical major histocompatibility complex class II (MHC-II)-like molecule H2-O, a negative regulator of antigen presentation. The recessive and functionally null I/LnJ H2-Ob allele supported the production of virus-neutralizing antibodies independently of the classical MHC haplotype. Subsequent bioinformatics and functional analyses of the human H2-Ob homolog, HLA-DOB, revealed both loss- and gain-of-function alleles, which could affect the ability of their carriers to control infections with human hepatitis B (HBV) and C (HCV) viruses. Thus, understanding of the previously unappreciated role of H2-O (HLA-DO) in immunity to infections may suggest new approaches in achieving neutralizing immunity to viruses.

摘要

人类和动物通过包括产生中和抗体在内的适应性免疫反应来控制持续性病毒感染。这种控制的确切遗传基础仍然不明。在此,我们报告了负责I/LnJ品系小鼠产生逆转录病毒中和抗体的基因的定位克隆。它编码非经典主要组织相容性复合体II类(MHC-II)样分子H2-O的β亚基,H2-O是抗原呈递的负调节因子。隐性且功能缺失的I/LnJ H2-Ob等位基因独立于经典MHC单倍型支持病毒中和抗体的产生。随后对人类H2-Ob同源物HLA-DOB的生物信息学和功能分析揭示了功能丧失和功能获得等位基因,它们可能影响其携带者控制人类乙型肝炎(HBV)和丙型肝炎(HCV)病毒感染的能力。因此,了解H2-O(HLA-DO)在抗感染免疫中以前未被认识的作用可能会为实现病毒中和免疫提供新方法。

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