PLoS Pathogens · 2019 · 19 citations · 34 references
Life SciencesImmunologyInfectious DiseasesInnate ImmunityMucosal ImmunologyVirologyB Cell ActivationB Cell BiologyB Cell DevelopmentB-cell ResponsesHumoral ImmunityInnate Immune ResponseB Cell Responses To InfectionB Cell-mediated ImmunityB-cell ImmunophenotypesB-cell Mediated ImmunityMarginal Zone B Cell DevelopmentMarginal Zone B CellsMucosal B Cell ImmunityMucosal B Cells
BLyS/BAFF is recognized for its role in B-cell ontogenesis, as well as cell fate decision towards the first-line/innate marginal zone (MZ) B-cell pool. Excess BLyS/BAFF is associated with hyperglobulinemia and increased frequencies of activated precursor-like MZ B-cells. Herein, we show that HIV highly-exposed seronegative (HESN) commercial sex workers (CSWs) had lower soluble BLyS/BAFF levels and relative frequencies of BLyS/BAFF expressing cells in their genital mucosa when compared to those from HIV-infected CSWs and HIV-uninfected non-CSWs. Furthermore, we identified genital innate and/or marginal zone (MZ)-like CD1c+ B-cells that naturally bind to fully glycosylated gp120, which frequencies were lower in HESNs when compared to HIV-infected CSWs and HIV-uninfected non-CSWs. Although genital levels of total IgA were similar between groups, HESNs had lower levels of total IgG1 and IgG3. Interestingly, HIV-gp41 reactive IgG1 were found in some HESNs. Low genital levels of BLyS/BAFF observed in HESNs may allow for controlled first-line responses, contributing to natural immunity to HIV.
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