Changes in vaginal bacteria and inflammatory mediators from periconception through early-postpartum in a cohort of HIV-negative Kenyan women
Abstract
Background: Women’s increased risk of HIV acquisition during pregnancy and the postpartum period maybe mediated by changes in vaginal microbiota and/or cytokines.
Methods: A cohort of HIV-1-seronegative Kenyan women contributed vaginal fluid samples at six pregnancy
time points: periconception, positive pregnancy test, first trimester, second trimester, third trimester and
postpartum. Concentrations of vaginal bacteria previously associated with HIV risk and cytokines were
measured using quantitative polymerase chain reaction and immunoassays, respectively.
Results: Eighty women contributed 409 samples. Using Tobit regression, later pregnancy time points were
associated with lower concentrations of Sneathia spp. (p=0.01), Eggerthella sp. Type 1 (p=0.002) and
Parvimonas sp. Type 2 (p=0.02), and higher concentrations of IL-6 (p=3x10-5), TNF (p=0.004), CXCL10
(p=1x10-4), CCL3 (0.009), CCL4 (p=4.8x10-7), CCL5 (p=0.002), IL-1b (p=0.02), and IL-8 (p=0.002). Most
cervicovaginal cytokines and vaginal bacteria clustered separately in principal components analysis, except
for CXCL10, which did not group with either the cytokine or bacterial clusters. The shift toward a more
Lactobacillus dominated microbiota during pregnancy appeared to mediate the relationship between
pregnancy time point and CXCL10.
Conclusions: Increases in proinflammatory cytokines, but not vaginal bacterial taxa previously associated
with HIV risk, could provide an explanation for increased HIV susceptibility during pregnancy and
postpartum.
Description
Thesis (Master's)--University of Washington, 2023
