HIV-1感染的V3血清分型:与基因分型的相关性和局限性

J C Plantier, F Damond, M Lasky, J L Sankalé, C Apetrei, M Peeters, L Buzelay, S M'Boup, P Kanki, E Delaporte, F Simon, F Barin
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引用次数: 24

摘要

HIV-1 V3血清分型是一种基于抗体与V3肽结合的免疫缺陷病毒分类方法,可以获得关于循环亚型的信息,这对于基于人群的流行病学研究可能很重要。最近,一些实验室已经开发出V3 enzyme-immunoassays (EIA)使用V3肽的亚型大肠在目前的研究中,包括额外的肽的效用对H亚型F EIA是评估小组203良好的患者的血清样本多样化的地理起源(22个国家)和已知的hiv - 1基因型(79 A, 61 B, 21 C, 7 D, 7 E, 21 F, 6 G, 1 H)。结果表明预测价值高(ppv)血清型B (> = 0.86),D(1)和E(0.88),并证实了基于血清A型或C型预测基因A型或C型的难度。结果还表明,在V3 EIAs中包含F肽可能是有用的(ppv = 0.61),但引入肽G和H未能显示出对这些亚型的显著敏感性或特异性。103个样本V3区血清分型与氨基酸序列之间的相关性使得鉴定出对亚型特异性血清反应性至关重要的关键氨基酸。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
V3 serotyping of HIV-1 infection: correlation with genotyping and limitations.

HIV-1 V3 serotyping is a classification of immunodeficiency viruses based on antibody binding to V3 peptides that allows obtaining information on circulating subtypes that could be important for population-based epidemiologic studies. Recently, several laboratories have developed V3 enzyme-immunoassays (EIAs) using V3 peptides of subtypes A to E. In the present study, the utility of including additional peptides of subtypes F to H to the EIA was evaluated on a panel of 203 well-characterized serum samples from patients with diverse geographic origins (22 countries) and known HIV-1 genotype (79 A, 61 B, 21 C, 7 D, 7 E, 21 F, 6 G, 1 H). The results indicate a high predictive value (ppv) for serotypes B (> or =0.86), D (1) and E (0.88), and confirm the difficulty of predicting genotype A or C based on serotype A or C. Results also indicate that inclusion of the F peptide in the V3 EIAs may be useful (ppv = 0.61), but introduction of peptides G and H failed to demonstrate significant sensitivity or specificity for these subtypes. Correlation between serotyping and amino-acid sequences of the V3 region from 103 samples allowed the identification of key amino-acids that appear essential for subtype-specific seroreactivity.

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