Evidence map›Paper›PMID 19924635›Full record

ReviewThe International journal of developmental biology2010

Naturally acquired microchimerism.

Hilary S Gammill, J Lee Nelson

Open access · bronzeAbstract readReview
In one paragraph

Review in The International journal of developmental biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 87 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
87citing papers in PubMed, 1 pooled it
18.4field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

87 citing papers in PubMed, 1 synthesis or guideline pooled it, 174 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Motherhood, the "blank slate," and the language of surrogacy.Frontiers in global women's health · 2026
    Article
  8. Article
  9. Review
  10. The Microchimerism Literature Atlas.Bioinformatics and biology insights · 2025
    Article
  11. Article
  12. Review
  13. Presence of fetal microchimerisms in the heart and effect on cardiac repair.Frontiers in cell and developmental biology · 2024
    Article
  14. Article
  15. Article
  16. Microchimerism as Post-Transplant Marker of a Chronic Rejection Process.International journal of molecular sciences · 2023
    Article
  17. Article
  18. Increased fetal microchimerism in immune and stem cell subsets in preeclampsia.American journal of reproductive immunology (New York, N.Y. : 1989) · 2023
    Article
  19. Genetics of Sex Differences in Immunity.Current topics in microbiology and immunology · 2023
    Article
  20. Article

27 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 2 institutions in 2 countries.

Hilary S GammillDepartment of Clinical Research, Fred Hutchinson Cancer Research Center, University of Washington, Seattle, Washington, USA. hgammill@u.washington.edu
J Lee Nelson
Cancer Research Center · USFred Hutch Cancer Center · US

Funding

WOMEN'S REPRODUCTIVE HEALTH RESEARCH CAREER DEVELOPMENTK12HD001264 · NICHD · UNIVERSITY OF WASHINGTON · PI Barbara Ann Goff · 1998 to 2026
$8.6M
PREGNANCY, MICROCHIMERISM, AND AUTOIMMUNE DISEASER01AI041721 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI NELSON, J. LEE · 1997 to 2011
$4.2M
ALLOIMMUNITY IN AUTO IMMUNE DISEASER01AI045659 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI NELSON, J. LEE · 1999 to 2009
$3.4M
Transgenerational Microchimerism in Pregnancy LossR21AI072547 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI NELSON, J. LEE · 2007 to 2008
$483k
MICROCHIMERISM IN THE PATHOGENESIS OF PBCR03AI045952 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI NELSON, J. LEE LEE · 1999 to 2000
$87k
NIAID NIH HHS R01 AI041721NIAID NIH HHS R01 AI045659NIAID NIH HHS R03 AI045952NIAID NIH HHS R21 AI072547NICHD NIH HHS K12 HD001264
6 · The paper itself

Abstract

Bi-directional transplacental trafficking occurs routinely during the course of normal pregnancy, from fetus to mother and from mother to fetus. In addition to a variety of cell-free substances, it is now well recognized that some cells are also exchanged. Microchimerism refers to a small number of cells (or DNA) harbored by one individual that originated in a genetically different individual. While microchimerism can be the result of iatrogenic interventions such as transplantation or transfusion, by far the most common source is naturally acquired microchimerism from maternal-fetal trafficking during pregnancy. Microchimerism is a subject of much current interest for a number of reasons. During pregnancy, fetal microchimerism can be sought from the mothers blood for the purpose of prenatal diagnosis. Moreover, studies of fetal microchimerism during pregnancy may offer insight into complications of pregnancy, such as preeclampsia, as well as insights into the pathogenesis of autoimmune diseases such as rheumatoid arthritis which usually ameliorates during pregnancy. Furthermore, it is now known that microchimerism persists decades later, both fetal microchimerism in women who have been pregnant and maternal microchimerism in her progeny. Investigation of the long-term consequences of fetal and maternal microchimerism is another exciting frontier of active study, with initial results pointing both to adverse and beneficial effects. This review will provide an overview of microchimerism during pregnancy and of current knowledge regarding long-term effects of naturally acquired fetal and maternal microchimerism.

Indexed as

ChimerismAutoimmune DiseasesDNAFemaleHumansMaternal-Fetal ExchangePregnancyTimeDNA

Identifiers

PMID19924635
PMCPMC2887685
OpenAlexW1998455536

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.