Maclaine A Parish, Jaiprasath Sachithanandham, Lizeth Gutierrez, Han-Sol Park, Anna Yin, Katerina Roznik, Patrick Creisher, John S Lee, Laura A St Clair, Annie Werner, Susan Bersoff-Matcha, Catherine Pilgrim-Grayson, Lee Berhane, Hana Golding, Patrick Shea, Katherine Fenstermacher, Richard Eric Rothman, Irina Burd, Jeanne Sheffield, Andrea L Cox, Andrew Pekosz, Sabra Klein
{"title":"Pregnancy Reduces COVID-19 Vaccine Immunity Against Novel Variants.","authors":"Maclaine A Parish, Jaiprasath Sachithanandham, Lizeth Gutierrez, Han-Sol Park, Anna Yin, Katerina Roznik, Patrick Creisher, John S Lee, Laura A St Clair, Annie Werner, Susan Bersoff-Matcha, Catherine Pilgrim-Grayson, Lee Berhane, Hana Golding, Patrick Shea, Katherine Fenstermacher, Richard Eric Rothman, Irina Burd, Jeanne Sheffield, Andrea L Cox, Andrew Pekosz, Sabra Klein","doi":"10.1101/2025.01.29.25321357","DOIUrl":null,"url":null,"abstract":"<p><p>Pregnant women are at heightened risk for severe outcomes from infectious diseases like COVID-19, yet were not included in initial vaccine trials, which may contribute to low booster uptake (15% or lower). We explored the serological and cellular responses to COVID-19 mRNA booster vaccines (i.e., ancestral and BA.5) in pregnant and age-matched, non-pregnant females to identify how pregnancy affects immunity against vaccine and novel variants. Antibodies from pregnant women were less cross-reactive to non-vaccine antigens, including XBB.1.5 and JN.1. Non-pregnant females showed greater IgG1:IgG3 ratios and neutralization against all variants. In contrast, pregnant women had lower IgG1:IgG3 ratios and neutralization but increased antibody-dependent NK cell cytokine production and neutrophil phagocytosis, especially against novel variants. Pregnancy increased memory CD4+ T cells IFNγ production, monofunctional dominance, and fatty acid oxidation. Pregnancy may reduce the breadth, composition, and magnitude of humoral and cellular immunity, particularly in response to novel variants.</p>","PeriodicalId":94281,"journal":{"name":"medRxiv : the preprint server for health sciences","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-07-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11838623/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"medRxiv : the preprint server for health sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2025.01.29.25321357","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Pregnant women are at heightened risk for severe outcomes from infectious diseases like COVID-19, yet were not included in initial vaccine trials, which may contribute to low booster uptake (15% or lower). We explored the serological and cellular responses to COVID-19 mRNA booster vaccines (i.e., ancestral and BA.5) in pregnant and age-matched, non-pregnant females to identify how pregnancy affects immunity against vaccine and novel variants. Antibodies from pregnant women were less cross-reactive to non-vaccine antigens, including XBB.1.5 and JN.1. Non-pregnant females showed greater IgG1:IgG3 ratios and neutralization against all variants. In contrast, pregnant women had lower IgG1:IgG3 ratios and neutralization but increased antibody-dependent NK cell cytokine production and neutrophil phagocytosis, especially against novel variants. Pregnancy increased memory CD4+ T cells IFNγ production, monofunctional dominance, and fatty acid oxidation. Pregnancy may reduce the breadth, composition, and magnitude of humoral and cellular immunity, particularly in response to novel variants.