COVID-19 mRNA vaccines are immunogenic in pregnant and lactating women, study finds

In a new study from Beth Israel Deaconess Medical Center (BIDMC), specialists in the Department of Obstetrics and Gynecology and the Center for Virology and Vaccine Research evaluated the immunogenicity of COVID-19 mRNA vaccines in pregnant and lactating women who received either the Pfizer or Moderna COVID-19 vaccines. The researchers found that both vaccines triggered immune responses in pregnant and lactating women. Further analyses revealed that maternal vaccine antibodies are transferred into infant cord blood and breast milk. The team's findings appear today in the Journal of the American Medical Association.

"Our study supports the use of vaccines in pregnant and lactating individuals. The vaccine-elicited antibodies we detected in both infant cord blood and breast milk suggest that vaccinating pregnant mothers may potentially protect infants from COVID-19 infection," said lead author Ai-ris Y. Collier, MD, a Maternal-Fetal Medicine specialist at BIDMC. "Future research should focus on determining the timing of vaccination that optimizes delivery of antibodies through the placenta and breast milk to newborns."

Collier and colleagues conducted an exploratory, descriptive study of 103 women, ages 18-45, who received an mRNA COVID-19 vaccine (54 percent received Pfizer; 46 percent received Moderna). The scientists found similar levels of vaccine-induced antibody function and T cell responses in all non-pregnant, pregnant and lactating women after their second vaccine dose. Additionally, both pregnant and non-pregnant women who received the mRNA vaccines developed cross-reactive immune responses against the COVID-19 variants of concern B.1.1.7 and B.1.351.

"The COVID-19 mRNA vaccines raised robust immune responses in pregnant, lactating, and non-pregnant non-lactating women," said senior corresponding author Dan. H. Barouch, MD, PhD, Director of the Center for Virology and Vaccine Research at BIDMC. "Additionally, the vaccine-elicited antibody responses were greater than antibody responses seen after COVID-19 infections. These findings add to the emerging data that support the use of these vaccines in pregnant and lactating women."

Co-authors included Katherine McMahan, Jingyou Yu, Lisa H. Tostanoski, Ricardo Aguayo, Jessica Ansel, Abishek Chandrashekar, Shivani Patel, Esther A. Bondzie, Daniel Sellers, Julia Barrett, Owen Sanborn, Huahua Wan, Aiquan Chang, Tochi Anioke, Joseph Nkolola, Connor Bradshaw, Catherine Jacob-Dolan, Makda Gebre, Erica N. Borducchi, Jinyan Liu, Michele R. Hacker of BIDMC; Jared Feldman, Aaron G. Schmidt and Galit Alter of the Ragon Institute of MGH, MIT, and Harvard; Todd Suscovich and Caitlyn Linde of Seromyx Systems.

This works was supported by the National Institutes of Health (CA260476, AI146779), Ragon Institute of MGH, MIT, and Harvard, Massachusetts Consortium for Pathogen Readiness, Musk Foundation, Reproductive Scientist Development Program from the Eunice Kennedy Shriver National Institute of Child Health & Human Development and Burroughs Wellcome Fund (HD000849), Multidisciplinary AIDS Training Program (AI007387), and the Harvard Clinical and Translational Science Center (TR002541)