Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
National Laboratory for HIV Genetics, National Microbiology Laboratories, Public Health Agency of Canada, Winnipeg, Manitoba, Canada.
JCI Insight. 2023 Jun 8;8(11):e170068. doi: 10.1172/jci.insight.170068.
Biological sex and host genetics influence HIV pathogenesis. Females have a higher likelihood of spontaneous viral control and lower set point viral load (spVL). No prior studies have assessed sex-specific genetics of HIV. To address this, we performed a sex-stratified genome-wide association study using data from the ICGH. Although it is the largest collection of genomic data in HIV, this multiethnic sample of 9,705 people is 81.3% male. We sought to identify sex-specific genetic variants and genes associated with HIV spVL and control. We confirmed associations in the HLA and CCR5 regions in males and HLA in females. Gene-based analyses detected associations between HIV spVL and PET100, PCP2, XAB2, and STXBP2 only in males. We detected variants with a significant sex-differential effect on spVL in SDC3 and PUM1 (rs10914268) and PSORS1C2 (rs1265159) and on HIV control in SUB1 (rs687659), AL158151.3, PTPA, and IER5L (rs4387067). Those variants have epigenetic and genetic interactions with relevant genes with both cis and trans effects. In summary, we identified sex-shared associations at the single-variant level, sex-specific associations at the gene-based level, and genetic variants with significant differential effects between the sexes.
生物性别和宿主遗传影响 HIV 发病机制。女性具有更高的自发病毒控制可能性和更低的设定点病毒载量(spVL)。先前没有研究评估过 HIV 的性别特异性遗传。为了解决这个问题,我们使用 ICGH 的数据进行了性别分层的全基因组关联研究。尽管这是 HIV 中最大的基因组数据集,但这个由 9705 人组成的多民族样本中 81.3%是男性。我们试图确定与 HIV spVL 和控制相关的性别特异性遗传变异和基因。我们在男性中确认了 HLA 和 CCR5 区域以及女性中的 HLA 区域的关联。基于基因的分析检测到 HIV spVL 与 PET100、PCP2、XAB2 和 STXBP2 之间仅在男性中存在关联。我们检测到 SDC3 和 PUM1(rs10914268)以及 PSORS1C2(rs1265159)中对 spVL 具有显著性别差异效应的变体,以及 SUB1(rs687659)、AL158151.3、PTPA 和 IER5L(rs4387067)中对 HIV 控制具有显著性别差异效应的变体。这些变体与 cis 和 trans 效应的相关基因具有表观遗传和遗传相互作用。总之,我们在单变体水平上发现了性别共享的关联,在基于基因的水平上发现了性别特异性的关联,以及在性别之间具有显著差异效应的遗传变体。