# Schistosoma Mansoni Infection During Pregnancy: Dissecting the Implications to Fetal Immunity > **NIH NIH R01** · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · 2021 · $462,499 ## Abstract Maternal helminth infections have been implicated in the reduced efficacy of critical life-saving neonatal and childhood immunizations. Approximately 40 million women of childbearing age are at risk for schistosomiasis and at least 10 million women in Africa have schistosomiasis during pregnancy, yet little is known about the impact of prenatal exposure on the immune responsiveness of offspring. Findings from previous studies indicate that a fetus can be exposed to helminth antigens in utero, so the high frequency of schistosomiasis in this population represents a significant potential public health problem. The WHO recently recommended anthelminthic treatments for all pregnant women who test helminth positive; however, very few studies have evaluated the immunological impact of drug treatment on either the mother or the fetus. Anthelminthic treatment and the resultant release of parasite antigens have the potential to sensitize a fetus in much the same way that natural infection does. Given the potentially serious adverse pathological and immunological consequences of both maternal infection and anthelminthic treatment, it is critical that we understand the immunological consequences of prenatal helminth infection, so that appropriate recommendations can be formulated to address any issues with current practices and, ultimately, help to improve immune responses in infants in resource-poor countries. Our objective in this proposal is to determine the immunological mechanism(s) through which prenatal S. mansoni infection modulates the homeostatic immune environment, and the effect this immune-modulation has on post-natal immune responses to antigenic challenge in a mouse model of maternal S. mansoni infection. Our central hypothesis is that in utero exposure to S. mansoni antigens reduces the steady-state expression of the co-stimulatory molecules CD21/35, and preconditions lymph nodes in the developing fetus towards a muted Th2-skewed immune response following postnatal immunization with immunologically unrelated antigens. We propose three specific aims to test this: 1) Define the mechanism(s) by which prenatal exposure of mice to S. mansoni infection modulates postnatal peripheral lymph node homeostasis; 2) Define the mechanism(s) by which prenatal exposure to S. mansoni infection modulates postnatal cellular immune responses to unrelated antigenic challenge; 3) Determine the consequences of anthelminthic treatment of infected pregnant mice on postnatal vaccine-induced immunity of offspring. At the completion of these studies, we expect to have identified key immunological mechanisms that underlie reduced immunity in offspring born to mothers infected with S. mansoni. It is likely these mechanisms will include reduced antigen presentation ability and preconditioning of antigen presenting cells and the T cell compartment towards priming a Th2 response; however even if it is not, we expect to have identified key mechanisms underlying reduced immun... ## Key facts - **NIH application ID:** 10092908 - **Project number:** 5R01AI135045-05 - **Recipient organization:** UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH - **Principal Investigator:** Keke Celeste Fairfax - **Activity code:** R01 (R01, R21, SBIR, etc.) - **Funding institute:** NIH - **Fiscal year:** 2021 - **Award amount:** $462,499 - **Award type:** 5 - **Project period:** 2018-02-01 → 2023-01-31 ## Primary source NIH RePORTER: https://reporter.nih.gov/project-details/10092908 ## Citation > US National Institutes of Health, RePORTER application 10092908, Schistosoma Mansoni Infection During Pregnancy: Dissecting the Implications to Fetal Immunity (5R01AI135045-05). Retrieved via AI Analytics 2026-05-23 from https://api.ai-analytics.org/grant/nih/10092908. Licensed CC0. --- *[NIH grants dataset](/datasets/nih-grants) · CC0 1.0*