» Articles » PMID: 37610043

Pregnancy-induced Transfer of Pathogen-specific T cells from Mother to Fetus in Mice

Overview
Journal EMBO Rep
Specialty Molecular Biology
Date 2023 Aug 23
PMID 37610043
Authors
Affiliations
Soon will be listed here.
Abstract

Neonatal health is determined by the transfer of maternal antibodies from the mother to the fetus. Besides antibodies, maternal cells cross the placental barrier and seed into fetal organs. Contrary to maternal antibodies, maternal microchimeric cells (MMc) show a high longevity, as they can persist in the offspring until adulthood. Recent evidence highlights that MMc leukocytes promote neonatal immunity against early-life infections in mice and humans. As shown in mice, this promotion of immunity was attributable to an improved fetal immune development. Besides this indirect effect, MMc may be pathogen-specific and thus, directly clear pathogen threats in the offspring postnatally. By using ovalbumin recombinant Listeria monocytogenes (LmOVA), we here provide evidence that OVA-specific T cells are transferred from the mother to the fetus, which is associated with increased activation of T cells and a milder course of postnatal infection in the offspring. Our data highlight that maternally-derived passive immunity of the neonate is not limited to antibodies, as MMc have the potential to transfer immune memory between generations.

Citing Articles

The when, what, and where of naturally-acquired microchimerism.

Nelson J, Lambert N Semin Immunopathol. 2025; 47(1):20.

PMID: 40067465 DOI: 10.1007/s00281-024-01029-2.


Micro-to multi-chimerism: the multiple facets of a singular phenomenon.

Rinkevich B, Goulet T Semin Immunopathol. 2025; 47(1):17.

PMID: 39966117 DOI: 10.1007/s00281-025-01044-x.


Maternal microchimeric cell trafficking and its biological consequences depend on the onset of inflammation at the feto-maternal interface.

Slaats E, Bramreiter B, Chua K, Quilang R, Sallinger K, Eikmans M Semin Immunopathol. 2025; 47(1):8.

PMID: 39820729 PMC: 11742462. DOI: 10.1007/s00281-025-01037-w.


Pregnancy induced displacement of preexisting microchimeric cells in the absence of maternal B and T cells.

Pham G, Shao T, Kinder J, Peng Y, Turner L, Way S Front Immunol. 2024; 15:1478465.

PMID: 39539542 PMC: 11557343. DOI: 10.3389/fimmu.2024.1478465.


Deciphering the Role of Maternal Microchimerism in Offspring Autoimmunity: A Narrative Review.

Mpakosi A, Sokou R, Theodoraki M, Iacovidou N, Cholevas V, Kaliouli-Antonopoulou C Medicina (Kaunas). 2024; 60(9).

PMID: 39336498 PMC: 11433734. DOI: 10.3390/medicina60091457.


References
1.
Masopust D, Vezys V, Marzo A, Lefrancois L . Preferential localization of effector memory cells in nonlymphoid tissue. Science. 2001; 291(5512):2413-7. DOI: 10.1126/science.1058867. View

2.
Masopust D, Vezys V, Usherwood E, Cauley L, Olson S, Marzo A . Activated primary and memory CD8 T cells migrate to nonlymphoid tissues regardless of site of activation or tissue of origin. J Immunol. 2004; 172(8):4875-82. DOI: 10.4049/jimmunol.172.8.4875. View

3.
Maloney S, Smith A, Furst D, Myerson D, Rupert K, Evans P . Microchimerism of maternal origin persists into adult life. J Clin Invest. 1999; 104(1):41-7. PMC: 408407. DOI: 10.1172/JCI6611. View

4.
Dave V, Cardozo-Ojeda E, Mair F, Erickson J, Woodward-Davis A, Koehne A . Cervicovaginal Tissue Residence Confers a Distinct Differentiation Program upon Memory CD8 T Cells. J Immunol. 2021; 206(12):2937-2948. PMC: 8642491. DOI: 10.4049/jimmunol.2100166. View

5.
Nguyen N, Olsen A, Lorenzen E, Andersen P, Hvid M, Follmann F . Parenteral vaccination protects against transcervical infection with and generate tissue-resident T cells post-challenge. NPJ Vaccines. 2020; 5(1):7. PMC: 6978417. DOI: 10.1038/s41541-020-0157-x. View