Department of Medicine, University of Washington, Seattle, Washington, USA.
Department of Global Health, University of Washington, Seattle, Washington, USA.
J Infect Dis. 2023 Aug 16;228(4):487-499. doi: 10.1093/infdis/jiad168.
Women's increased risk of HIV acquisition during pregnancy and postpartum may be mediated by changes in vaginal microbiota and/or cytokines.
A cohort of 80 Kenyan women who were HIV-1 seronegative contributed 409 vaginal samples at 6 pregnancy time points: periconception, positive pregnancy test result, first trimester, second trimester, third trimester, and postpartum. Concentrations of vaginal bacteria linked with HIV risk and Lactobacillus spp were measured using quantitative polymerase chain reaction. Cytokines were measured by immunoassay.
Based on Tobit regression, later pregnancy time points were associated with lower concentrations of Sneathia spp (P = .01), Eggerthella sp type 1 (P = .002), and Parvimonas sp type 2 (P = .02) and higher concentrations of Lactobacillus iners (P < .001), Lactobacillus crispatus (P < .001), Lactobacillus vaginalis (P < .001), interleukin 6 (P < .001), TNF (P = .004), C-X-C motif chemokine ligand 10 (CXCL10; P < .001), C-C motif ligand 3 (P = .009), C-C motif ligand 4 (P < .001), C-C motif ligand 5 (P = .002), interleukin 1β (P = .02), and interleukin 8 (P = .002). Most cervicovaginal cytokines and vaginal bacteria clustered separately in principal component analysis, except for CXCL10, which did not group with either cytokines or bacteria. The shift toward a Lactobacillus-dominated microbiota during pregnancy mediated the relationship between pregnancy time point and CXCL10.
Increases in proinflammatory cytokines, but not vaginal bacterial taxa linked with higher HIV risk, could provide an explanation for increased HIV susceptibility during pregnancy and postpartum.
女性在怀孕期间和产后获得 HIV 的风险增加,这可能是阴道微生物群和/或细胞因子发生变化所致。
一个由 80 名肯尼亚 HIV-1 血清阴性女性组成的队列,在怀孕的 6 个时间点(受孕前、妊娠阳性测试结果、孕早期、孕中期、孕晚期和产后)共提供了 409 份阴道样本。使用定量聚合酶链反应测量与 HIV 风险相关的阴道细菌和乳杆菌属的浓度。通过免疫测定测量细胞因子。
基于 Tobit 回归,妊娠后期时间点与较低的 Sneathia spp 浓度相关(P =.01)、Eggerthella sp type 1(P =.002)和 Parvimonas sp type 2(P =.02),而较高的 Lactobacillus iners(P <.001)、Lactobacillus crispatus(P <.001)、Lactobacillus vaginalis(P <.001)、白细胞介素 6(P <.001)、肿瘤坏死因子(P =.004)、C-X-C 基序趋化因子配体 10(CXCL10;P <.001)、C-C 基序配体 3(P =.009)、C-C 基序配体 4(P <.001)、C-C 基序配体 5(P =.002)、白细胞介素 1β(P =.02)和白细胞介素 8(P =.002)。大多数宫颈阴道细胞因子和阴道细菌在主成分分析中单独聚类,除了 CXCL10 之外,它与细胞因子或细菌都没有分组。在怀孕期间向乳杆菌主导的微生物群的转变介导了妊娠时间点与 CXCL10 之间的关系。
促炎细胞因子的增加,而不是与更高 HIV 风险相关的阴道细菌分类群的增加,可能为怀孕期间和产后 HIV 易感性增加提供了解释。