Evidence map›Paper›PMID 20553337›Full record

ArticleImmunology2010

Evidence that CD8 T-cell homeostasis and function remain intact during murine pregnancy.

Michelle T Norton, Karen A Fortner, Karen H Oppenheimer, Elizabeth A Bonney

Open access · bronzeAbstract read
In one paragraph

Article in Immunology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

27 citing papers in PubMed, 45 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. The landscape of decidual immune cells at the maternal-fetal interface in parturition and preterm birth.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2025
    Review
  5. Article
  6. A Framework for Understanding Maternal Immunity.Immunology and allergy clinics of North America · 2023
    Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Influenza in High-Risk Hosts-Lessons Learned from Animal Models.Cold Spring Harbor perspectives in medicine · 2020
    Review
  12. Review
  13. Are B cells altered in the decidua of women with preterm or term labor?American journal of reproductive immunology (New York, N.Y. : 1989) · 2019
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Immune Regulation in Pregnancy: A Matter of Perspective?Obstetrics and gynecology clinics of North America · 2016
    Review
  20. Article
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

4 authors at 1 institution in 1 country.

Michelle T NortonUniversity of Vermont College of Medicine, Department of Obstetrics, Gynecology, and Reproductive Sciences, Burlington, VT 05405, USA.
Karen A Fortner
Karen H Oppenheimer
Elizabeth A Bonney
University of Vermont · US

Funding

VERMONT IMMUNOBIOLOIGY/ INFECTIOUS DISEASES CENTERP20RR021905 · NCRR · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI MATRAJT, MARIANA L · 2006 to 2011
$14.5M
Vermont Immunobioloigy/ Infectious Diseases CenterP20GM103496 · NIGMS · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI BUDD, RALPH C · 2012 to 2015
$8.7M
FAS REGULATES T CELL DEVELOPMENT/FUNCTION IN LPR MICER01AI036333 · NIAID · UNIVERSITY OF VERMONT &ST AGRIC COLLEGE · PI BUDD, RALPH C · 1996 to 2010
$3.7M
Vermont Immunology/Infectious Diseases Training GrantT32AI055402 · NIAID · UNIVERSITY OF VERMONT &ST AGRIC COLLEGE · PI GARY E WARD · 2005 to 2026
$2.7M
Pregnancy and T cell homeostasisR01HD043185 · NICHD · UNIVERSITY OF VERMONT &ST AGRIC COLLEGE · PI BONNEY, ELIZABETH A · 2003 to 2006
$949k
NCRR NIH HHS P20 RR021905NIAID NIH HHS AI0797112NIAID NIH HHS AI36333NIAID NIH HHS R01 AI036333NIAID NIH HHS T-32AI055402NIAID NIH HHS T32 AI055402NICHD NIH HHS R01 HD043185NICHD NIH HHS R01-HD043185NIGMS NIH HHS P20 GM103496
6 · The paper itself

Abstract

Evolving models of immune tolerance have challenged the view that the response of the maternal immune system to environmental or fetal antigens must be suppressed or deviated. CD8 T cells play a central role in the immune response to viruses and intracellular pathogens so the maintenance of both the number and function of these cells is critical to protect both the mother and fetus. We show that the numbers of maternal CD8 T cells in both the spleen and the uterine draining lymph nodes are transiently increased at mid-gestation and this correlates with enhanced CD8 T-cell proliferation and an increased relative expression of both pro-survival and pro-apoptotic molecules. In transgenic mice bearing T-cell antigen receptors specific for the male HY or allo-antigens, the transgenic CD8 T cells retain the ability to proliferate and function during pregnancy. Moreover, anti-HY T-cell receptor transgenic mice have normal numbers of male pups despite the presence of CD8 T cells at the maternal-fetal interface. These data suggest that pregnancy is a dynamic state in which CD8 T-cell turnover is increased while the function and ending size of the CD8 T-cell compartment are maintained.

Indexed as

HomeostasisAnimalsApoptosisCD8-Positive T-LymphocytesCell CountCell ProliferationCells, CulturedFas Ligand ProteinFemaleH-Y AntigenImmune ToleranceInterleukin-7 Receptor alpha SubunitLitter SizeMiceMice, Inbred BALB CMice, Inbred C57BLFas Ligand ProteinH-Y AntigenInterleukin-7 Receptor alpha SubunitProto-Oncogene Proteins c-bcl-2Receptors, Antigen, T-Cell

Identifiers

PMID20553337
PMCPMC2996563
OpenAlexW2157521232

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.