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Active NON-SBIR/STTR RPGS NIH (US)

Dynamic changes in virome-host interactions during pregnancy and postpartum

$11.45M USD

Funder NATIONAL CENTER FOR COMPLEMENTARY & INTEGRATIVE HEALTH
Recipient Organization Washington University
Country United States
Start Date Sep 17, 2024
End Date Aug 31, 2029
Duration 1,809 days
Number of Grantees 3
Roles Co-Investigator; Principal Investigator
Data Source NIH (US)
Grant ID 10986490
Grant Description

Abstract For more than a decade the importance of the microbiome and its role in health and disease has been appreciated, yet the virome (the viral component of the microbiome) has remained understudied. Physiologic changes during pregnancy and the postpartum period (often overlooked periods of the lifespan) include

dramatic adaptations in immune response that provide a unique opportunity to study and understand the dynamic interplay between the virome and host. Both systemic and local modifications in innate and adaptive immunity have been described, characterizing an “immunological clock” of pregnancy. These programmed

changes in immune response are critical for pregnancy success, providing a balance between fetal tolerance and effective protection from pathogens, including viruses. Individual viruses that cause adverse pregnancy outcomes have been frequently studied, for example those that cause more severe infection during pregnancy

and those that cause congenital infections. However, the complex communities of the virome (in this case defined as all the viruses that infect human cells) have largely remained unexplored. We hypothesize that the dynamic, programmed changes in immune response through pregnancy and postpartum will alter the

interactions between virome and host, revealing important underlying biology of the virome-maternal-fetal unit. To test this hypothesis, we will prospectively collect longitudinal samples from the pregnancy, delivery, and postpartum periods in a racially diverse cohort of 100 subjects enrolled at two sites to monitor the virome in

tandem with local and systemic immune responses.

All Grantees

Washington University

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