首页> 外文期刊>Infection, Genetics and Evolution: Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases >Effect of the maturation of neutralizing antibodies on human immunodeficiency virus (HIV) envelope evolution in HIV-infected subjects
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Effect of the maturation of neutralizing antibodies on human immunodeficiency virus (HIV) envelope evolution in HIV-infected subjects

机译:中和抗体的成熟对感染HIV的受试者的人体免疫缺陷病毒(HIV)包膜进化的影响

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Delineating the course of NAb (neutralizing antibody) development in natural infection may provide clues for NAb-targeted HIV-1 vaccine design. Two subjects, A (non-neutralizer) and E (neutralizer), were chosen from 75 HIV-1 positive subjects of a MSM (men who have sex with men) cohort to investigate the key events of virus evolution in the development course of neutralizing antibodies. Pseudovirus quasispecies (at least 10 strains) were generated for each time points of the infection course. The diversity and divergence of the env quasispecies per time point for subject E were significantly higher than those for subject A (p 0.05). Compared with subject A, the gp160 derived from subject E acquired longer V1V2 region and more N-glycans during the development of neutralizing antibodies. The developing course of neutralizing antibody lagged behind the virus evolution, of which the pseudoviruses could only been neutralized by the latter time-point sera. The neutralization-driven evolution of the virus for subject E was mostly mapped to the C1-C3 region of gp160. Through site-directed mutagenesis, some key sites and region were identified to be associated with the virus escape, including: Q85P, H183P, K340E, L365S, L369I, I372V and insertions of 355 N in C3 and NITDEVKIG in V1 region. (C) 2015 Elsevier B.V. All rights reserved.
机译:描绘自然感染中NAb(中和抗体)的发展过程可能为靶向NAb的HIV-1疫苗设计提供线索。从MSM(男男性接触者)队列的75个HIV-1阳性受试者中选择了两个受试者(非中和剂)和E(中和剂),以研究病毒在中和发展过程中进化的关键事件抗体。在感染过程的每个时间点都产生了伪病毒准种(至少10个毒株)。受试者E在每个时间点的准准种的多样性和差异显着高于受试者A(p <0.05)。与受试者A相比,源自受试者E的gp160在中和抗体的形成过程中获得了更长的V1V2区和更多的N-聚糖。中和抗体的发展过程落后于病毒的进化,其中伪病毒只能被后者的时间点血清中和。针对受试者E的病毒的中和驱动进化主要定位于gp160的C1-C3区域。通过定点诱变,确定了一些与病毒逃逸相关的关键位点和区域,包括:Q85P,H183P,K340E,L365S,L369I,I372V以及在C3中插入了355 N,在V1地区中插入了NITDEVKIG。 (C)2015 Elsevier B.V.保留所有权利。

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