Author:
Bebell Lisa M.,Ngonzi Joseph,Butler Audrey,Kumbakumba Elias,Adong Julian,Loos Carolin,Boatin Adeline A.,Bassett Ingrid V.,Siedner Mark J.,Williams Paige L.,Mattie Heather,Hedt-Gauthier Bethany,Correia Katharine F. B.,Lake Erin,Alter Galit
Abstract
AbstractDuring pregnancy, multiple immune regulatory mechanisms establish an immune-tolerant environment for the allogeneic fetus, including cellular signals called cytokines that modify immune responses. However, the impact of maternal HIV infection on these responses is incompletely characterized. We analyzed paired maternal and umbilical cord plasma collected during labor from 147 people with HIV taking antiretroviral therapy and 142 HIV-uninfected comparators. Though cytokine concentrations were overall similar between groups, using Partial Least Squares Discriminant Analysis we identified distinct cytokine profiles in each group, driven by higher IL-5 and lower IL-8 and MIP-1α levels in pregnant people with HIV and higher RANTES and E-selectin in HIV-unexposed umbilical cord plasma (P-value < 0.01). Furthermore, maternal RANTES, SDF-α, gro $$\mathrm{\alpha }$$
α
-KC, IL-6, and IP-10 levels differed significantly by HIV serostatus (P < 0.01). Although global maternal and umbilical cord cytokine profiles differed significantly (P < 0.01), umbilical cord plasma profiles were similar by maternal HIV serostatus. We demonstrate that HIV infection is associated with a distinct maternal plasma cytokine profile which is not transferred across the placenta, indicating a placental role in coordinating local inflammatory response. Furthermore, maternal cytokine profiles in people with HIV suggest an incomplete shift from Th2 to Th1 immune phenotype at the end of pregnancy.
Funder
Harvard University Center for AIDS Research
Harvard Catalyst
Charles H. Hood Foundation
National Institute of Allergy and Infectious Diseases
American Society of Tropical Medicine and Hygiene
National Institute of Allergy and Infectious Diseases,United States
Civic
Bill and Melinda Gates Foundation
Musk Foundation
Publisher
Springer Science and Business Media LLC