Skip to main content

PERSPECTIVE article

Front. Immunol.
Sec. Immunological Tolerance and Regulation
Volume 15 - 2024 | doi: 10.3389/fimmu.2024.1478465
This article is part of the Research Topic Antibody-Mediated Maternal and Fetal Conditions of Pregnancy View all articles

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

Provisionally accepted
Giang Pham Giang Pham Tzu-yu Shao Tzu-yu Shao Jeremy M. Kinder Jeremy M. Kinder Yanyan Peng Yanyan Peng Lucien H. Turner Lucien H. Turner Sing Sing Way Sing Sing Way *
  • Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, MN, United States

The final, formatted version of the article will be published soon.

    Bidirectional exchange of cells between mother and fetus occurs during pregnancy, and persistence of these genetically foreign cells establishes long-term microchimerism in both individuals after parturition. Since women can have multiple pregnancies, and all mothers were once daughters themselves, the microchimeric milieu in each woman could theoretically contain cells from a variety of origins, including from their own mothers as well as their babies from each pregnancy. Interestingly and in sharp contrast to this prediction, we recently showed preexisting populations of microchimeric cells are lost following pregnancy and associated with seeding of new fetal microchimeric cells. Complete loss of preexisting microchimeric cells in this context draws parallels to immunological rejection with synchronized elimination of cells and tissues that express defined discordant antigens. This perspective evaluates this provocative hypothesis regarding pregnancy induced rejection of microchimeric cells, including new experimental data comparing microchimerism levels in mice simultaneously lacking B and T cells before pregnancy, and after parturition with primary and secondary pregnancies.

    Keywords: Microchimaerism, RAG1, T cell, B cell, Non-inherited maternal antigen

    Received: 12 Aug 2024; Accepted: 11 Oct 2024.

    Copyright: © 2024 Pham, Shao, Kinder, Peng, Turner and Way. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

    * Correspondence: Sing Sing Way, Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, 55455, MN, United States

    Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.