Analysis of properties of HIV-1 subtype C envelope glycoprotein

HIV-1 C亚型包膜糖蛋白的特性分析

• 批准号: 8448272
• 负责人: Nina H. Lin
• 金额: $ 13.76万
• 依托单位: MASSACHUSETTS GENERAL HOSPITAL
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-05-01 至 2016-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8448272
• 关键词: AIDS prevention; Accounting; Address; Affect; Antibodies; Antibody Formation; Autologous; Biological; Biological Assay; Blood; Botswana; Breast Feeding; CXCR4 gene; Case-Control Studies; Cells; Child; Clinical; Clinical Data; Collaborations; DNA; Data; Disease Progression; Epidemiology; Epitopes; Evolution; Genes; Genetic; Genetic Determinism; Genetic Variation; Genotype; Glycoproteins; HIV; HIV-1; Heterophile Antibodies; Human Milk; Infant; Infection; Low Prevalence; Maps; Measures; Methods; Minor; Minority; Mothers; Mutation; Pathogenesis; Patients; Pattern; Phenotype; Plasma; Population; Predisposition; Pregnancy; Prevention strategy; Property; Prospective Studies; RNA; Research Personnel; Resolution; Risk; Route; Sample Size; Sampling; Sequence Analysis; Specimen; Surrogate Markers; T cell response; Techniques; Technology; Tropism; V3 Loop; Variant; Vertical Disease Transmission; Viral; Virus; Woman; Work; antiretroviral therapy; base; clinically significant; cohort; cross reactivity; design; disease transmission; genetic analysis; in utero; insight; neutralizing antibody; novel; pressure; prophylactic; public health relevance; pyrosequencing; therapy development; transmission process; treatment strategy; vaccine development

DESCRIPTION (provided by applicant): Many important biological determinants of HIV-1 disease progression and transmission map to the envelope glycoprotein, including antibody neutralization susceptibility, viral tropism for entry and epitopes for T cell response. Genetic and phenotypic characterizations of the envelope gene suggest a bottleneck effect in the spread of the virus to other body compartments and transmission, resulting in a predominantly homogenous viral population. However, the limitations in current methods to accurately assign HIV-1 coreceptor usage, distinguish genetic variations and detect minor variants in the HIV quasispecies within a patient and between transmission pairs have led to controversial findings. Furthermore, the small patient sample size studied has been too small to make broad generalization regarding mechanisms of HIV transmission and pathogensis. Lastly, these various properties of the envelope gene have been studied predominantly in subtype B infection and less clearly elucidated in HIV-1 subtype C, the most rapidly spreading and prevalent infection worldwide. We hypothesize that a heterogenous HIV-1 population with different envelope sequences and coreceptor usage are transmitted during infection but is not fully characterized and measured by our current available techniques. We propose to use novel and more sensitive methods to determine coreceptor usage and to perform in-depth sequencing and genetic analyses of the envelope gene from a large subtype C clinical cohort from Botswana. The envelope gene in subtype C infection will be studied in longitudinal samples, as well as between plasma-breast milk and mother-infant pairs. We plan to study in greater depth the properties of the HIV-1 subtype C envelope glycoprotein with the following specific aims: 1) identify clinical and genetic determinants of coreceptor switching, 2) assess for correlates of breastfeeding transmission of HIV-1 and 3) examine pattern of viral transmission among mother-to-child transmitting pairs occurring through different routes of MTCT using ultradeep sequencing. The results of this study will further the understanding of viral evolution in the context of transmission and disease progression, identify clinical correlates of transmission and disease progression, and ultimately give insights into potential strategies of prevention, treatment and vaccine development in those parts of the world most affected by HIV.

描述（由申请人提供）：HIV-1疾病进展和传播的许多重要生物学决定因素与包膜糖蛋白相关，包括抗体中和易感性、病毒进入性和T细胞反应的表位。包膜基因的遗传和表型特征表明，在病毒向其他身体隔室的传播和传播中存在瓶颈效应，导致病毒种群主要是同质的。然而，目前的方法在准确分配HIV-1共受体使用、区分遗传变异和检测患者体内HIV准种和传播对之间的微小变异方面存在局限性，导致了有争议的发现。此外，研究的患者样本量太小，无法对HIV传播和致病机制做出广泛的概括。最后，包膜基因的这些不同特性主要在B型感染中被研究，而在全球传播最迅速和流行的HIV-1 C型感染中不太清楚地阐明。我们假设具有不同包膜序列和辅助受体使用的异质HIV-1人群在感染期间传播，但目前可用的技术尚未完全表征和测量。我们建议使用新颖和更敏感的方法来确定辅助受体的使用，并对来自博茨瓦纳的大型C亚型临床队列的包膜基因进行深入的测序和遗传分析。C亚型感染的包膜基因将在纵向样本以及血浆-母乳和母婴对之间进行研究。我们计划更深入地研究HIV-1亚型C包膜糖蛋白的特性，具体目的如下：1)确定辅助受体转换的临床和遗传决定因素，2)评估母乳喂养HIV-1传播的相关性，以及3)使用超深度测序检测通过不同途径MTCT发生的母婴传播对之间的病毒传播模式。这项研究的结果将进一步了解传播和疾病进展背景下的病毒进化，确定传播和疾病进展的临床相关性，并最终为世界上受艾滋病毒影响最严重的地区的预防、治疗和疫苗开发的潜在策略提供见解。