Skip to content
DraconiticResearch
Search Sources API
203,234 studies31 sourcesUpdated 23 min ago
PreprintCC BY-NC-NDbioRxiv

Neonatal T cell maternal microchimerism is common and associates with early pregnancy SARS2 vaccination

5 affiliations
  1. 1Center for Global Infectious Disease Research, Seattle Children’s Research Institute, Seattle, WA
  2. 2Institute for Public Health Genetics, University of Washington School of Public Health, Seattle, WA
  3. 3Department of Obstetrics & Gynecology, University of Washington School of Medicine, Seattle, WA
  4. 4Department of Pediatrics, University of Washington School of Medicine, Seattle, WA
  5. 5Department of Global Health, University of Washington, Seattle, WA

Abstract

The fetus acquires a graft of maternal cells in utero, known as maternal microchimerism (MMc), which may be enriched for T cells. However, little is known regarding the determinants of T cell trafficking into the fetus or regarding the prevalence of T cell MMc in healthy neonates. Using a closely followed cohort, we determined the association between maternal vaccination and acute infection and the detection of T cell MMc in cord blood, as measured using polymorphism-specific qPCR. We identified an association between early pregnancy SARS2 mRNA vaccination, a potent T cell stimulus, and increased detection of T cell MMc.

Related

  1. Prenatal immune priming to Plasmodium falciparum is characterized by multi-lineage T-cell responses that are influenced by maternal microchimerism and predict malaria outcomes
    Y. Jiang, F. Bach, J. Houck +14
    bioRxivPreprintCC BYFull textImmunologybioRxiv
  2. Intranasal adenovirus type 5 influenza vaccination enhances milk antibody responses and passive transfer to neonatal ferrets
    L. S. Stafford, P. Baker, M. Moyer +10
    bioRxivPreprintCC BYFull textMicrobiologybioRxiv
  3. Pregnancy Impacts Maternal Sleep: Focus on Kynurenine Pathway Activation in Female Rats
    C. J. Wright, M. V. Piroli, J. H. Cox +3
    bioRxivPreprintAll rights reservedFull textNeurosciencebioRxiv
  4. Maternal gut microbiota, tryptophan metabolism and immune homeostasis: Implications for the prevention of adverse pregnancy complications
    Chenjun Wang, Siyu Wu, Biyan He +9
    iSciencePeer-reviewedCC BY-NC-ND 4.0Developmental biologyImmunologyCell PressCrossref
  5. From maternal microbial transmission to neonatal gut microbiota restoration: the potential and challenges of maternal fecal microbiota transplantation
    Xia Hu, Guangyu Ma, Jinbiao Han +3
    Frontiers in MicrobiologyPeer-reviewedCC BY 4.0MicrobiologyFrontiersCrossref
BibTeX
@misc{weaver2026neonatal,
  title = {{Neonatal T cell maternal microchimerism is common and associates with early pregnancy SARS2 vaccination}},
  author = {Jacquelyn Weaver and John Houck and Yonghou Jiang and Cara Tobey and Jia Wong and Swati Shree and Whitney E Harrington},
  howpublished = {bioRxiv},
  year = {2026},
  month = oct,
  doi = {10.64898/2026.10.23.761412},
  url = {https://www.biorxiv.org/content/10.64898/2026.10.23.761412v1},
  note = {CC BY-NC-ND},
}
RIS
TY  - UNPB
TI  - Neonatal T cell maternal microchimerism is common and associates with early pregnancy SARS2 vaccination
AU  - Jacquelyn Weaver
AU  - John Houck
AU  - Yonghou Jiang
AU  - Cara Tobey
AU  - Jia Wong
AU  - Swati Shree
AU  - Whitney E Harrington
PY  - 2026
DA  - 2026/10/23
PB  - bioRxiv
DO  - 10.64898/2026.10.23.761412
UR  - https://www.biorxiv.org/content/10.64898/2026.10.23.761412v1
AB  - The fetus acquires a graft of maternal cells in utero, known as maternal microchimerism (MMc), which may be enriched for T cells. However, little is known regarding the determinants of T cell trafficking into the fetus or regarding the prevalence of T cell MMc in healthy neonates. Using a closely followed cohort, we determined the association between maternal vaccination and acute infection and the detection of T cell MMc in cord blood, as measured using polymorphism-specific qPCR. We identified an association between early pregnancy SARS2 mRNA vaccination, a potent T cell stimulus, and increased detection of T cell MMc.
SN  - 2692-8205
ER  -