Evidence map›Paper›PMID 24553046›Full record

ArticleChimerism

Pregnancy-induced maternal regulatory T cells, bona fide memory or maintenance by antigenic reminder from fetal cell microchimerism?

Jeremy M Kinder, Tony T Jiang, Dayna R Clark, Vandana Chaturvedi, Lijun Xin, James M Ertelt, Sing Sing Way

Abstract read
In one paragraph

Article in Chimerism. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

  1. Review
  2. Review
  3. Immunologic Memory in Pregnancy: Focusing on Memory Regulatory T Cells.International journal of biological sciences · 2022
    Review
  4. Review
  5. Review
  6. Memory T Cells in Pregnancy.Frontiers in immunology · 2019
    Review
  7. Immunological memory cells.Central-European journal of immunology · 2018
    Review
  8. LowerJournal of immunology research · 2018
    Article
  9. Article
  10. Regulatory T cell memory.Nature reviews. Immunology · 2016
    Review
  11. Review
  12. Review
  13. Review
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

7 authors.

Jeremy M KinderDivision of Infectious Diseases; Cincinnati Children's Hospital Medical Center; Cincinnati, OH USA.
Tony T JiangDivision of Infectious Diseases; Cincinnati Children's Hospital Medical Center; Cincinnati, OH USA.
Dayna R ClarkDivision of Infectious Diseases; Cincinnati Children's Hospital Medical Center; Cincinnati, OH USA.
Vandana ChaturvediDivision of Infectious Diseases; Cincinnati Children's Hospital Medical Center; Cincinnati, OH USA.
Lijun XinDivision of Infectious Diseases; Cincinnati Children's Hospital Medical Center; Cincinnati, OH USA.
James M ErteltDivision of Infectious Diseases; Cincinnati Children's Hospital Medical Center; Cincinnati, OH USA.
Sing Sing WayDivision of Infectious Diseases; Cincinnati Children's Hospital Medical Center; Cincinnati, OH USA.

Funding

Medical Scientist Training ProgramT32GM063483 · NIGMS · UNIVERSITY OF CINCINNATI · PI KHURANA HERSHEY, GURJIT K. · 2002 to 2022
$6.7M
The Immune Pathogenesis of Prenatal Listeria monocytogenes InfectionR01AI100934 · NIAID · UNIVERSITY OF MINNESOTA · PI WAY, SING SING · 2012 to 2016
$2.3M
Regulatory T cells dictate immunity during persistent Salmonella infectionR01AI087830 · NIAID · UNIVERSITY OF MINNESOTA · PI WAY, SING SING · 2010 to 2014
$1.8M
CD4 T cells with specificity to noninherited maternal antigen.R21AI112186 · NIAID · CINCINNATI CHILDRENS HOSP MED CTR · PI WAY, SING SING · 2014 to 2015
$429k
NIAID NIH HHS R01 AI087830NIAID NIH HHS R01-AI087830NIAID NIH HHS R01 AI100934NIAID NIH HHS R01-AI100934NIAID NIH HHS R21 AI112186NIAID NIH HHS R21-AI112186NIGMS NIH HHS T32 GM063483
6 · The paper itself

Abstract

Long-term maintenance of immune components with defined specificity, without antigen is the hallmark feature of immunological memory. However, there are fundamental differences in how memory CD8(+) compared with CD4(+) T cells are maintained. After complete antigen elimination, CD8(+) T cells can persist as a self-renewing numerically stable cell population, and therefore satisfy the most stringent definition of "memory." Comparatively, CD4(+) T cell maintenance is considerably less stable, often requiring low-level antigen persistence or antigenic reminders. Recent studies show these basic memory features, classically ascribed to effector CD8(+) and CD4(+) T cells, extend to immune suppressive Foxp3(+) regulatory CD4(+) T cells (Tregs). In particular, gestational expansion and postpartum retention of maternal Tregs with fetal specificity may explain the protective benefits of primary pregnancy on complications in subsequent pregnancy. Herein, the possibility of ongoing antigenic reminders from fetal cell microchimerism in postpartum maintenance of maternal Tregs with fetal specificity is considered.

Indexed as

Immunologic MemoryMaternal-Fetal ExchangeAnimalsCD8-Positive T-LymphocytesChimeraEmbryo, MammalianFemaleHumansPregnancyT-Lymphocytes, Regulatoryimmunological memorymicrochimerismpregnancyregulatory T cellsT cells

Identifiers

PMID24553046
PMCPMC3988116

What OpenQuestion holds

Textmetadata
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.