Inherited maternal memory T cells protect offspring from respiratory viral infection through disease tolerance

Maternal immune transfer is a powerful mechanism for early-life protection from infection, yet the full repertoire of protective factors remains unknown. We discovered that maternal memory T cells are both necessary and sufficient to protect offspring from lethal respiratory infection. This antigen-specific protection operated independently of maternal antibodies and offspring T cell responses and required IL-10 produced by maternal T cells. Transfer of protective maternal T cells reduced offspring inflammatory responses and lung tissue damage without affecting viral burdens, indicating that maternal memory T cells directly suppress pathogenic innate inflammatory responses to preserve offspring health. Critically, maternal vaccination similarly protected offspring in a T cell-dependent manner. These findings reveal maternal antigen-specific T cell transfer as a complementary immunological defense mechanism to protect offspring against pathogens that escape maternal antibodies, with broad implications for maternal vaccination strategies.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-11-03
DOI
https://doi.org/10.64898/2026.10.30.763208
Primary Topic
T-cell and B-cell Immunology
Type
preprint
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preprint

Inherited maternal memory T cells protect offspring from respiratory viral infection through disease tolerance

Meghan A. Koch, Madelyn Cabán, Brittany Jimena, Emma E. Lederer et al.
bioRxiv (Cold Spring Harbor Laboratory)
T-cell and B-cell Immunology
preprint

Inherited maternal memory T cells protect offspring from respiratory viral infection through disease tolerance

Meghan A. Koch, Madelyn Cabán, Brittany Jimena, Emma E. Lederer, Whitney E. Harrington, Hamadoun Ibrahim Touré, Diane M. Rico, Saajidah Abideen, Addison Medlin McFadden, Pranav Kokati
preprint en

Abstract

Maternal immune transfer is a powerful mechanism for early-life protection from infection, yet the full repertoire of protective factors remains unknown. We discovered that maternal memory T cells are both necessary and sufficient to protect offspring from lethal respiratory infection. This antigen-specific protection operated independently of maternal antibodies and offspring T cell responses and required IL-10 produced by maternal T cells. Transfer of protective maternal T cells reduced offspring inflammatory responses and lung tissue damage without affecting viral burdens, indicating that maternal memory T cells directly suppress pathogenic innate inflammatory responses to preserve offspring health. Critically, maternal vaccination similarly protected offspring in a T cell-dependent manner. These findings reveal maternal antigen-specific T cell transfer as a complementary immunological defense mechanism to protect offspring against pathogens that escape maternal antibodies, with broad implications for maternal vaccination strategies.

bioRxiv (Cold Spring Harbor Laboratory)
Fred Hutch Cancer Center (US), Seattle Children's Research Institute (US)
T-cell and B-cell Immunology
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