Evidence map›Paper›PMID 9006326›Full record

ArticleThe American journal of pathology1997

T cell receptor-alpha beta-deficient mice fail to develop colitis in the absence of a microbial environment.

L Dianda, A M Hanby, N A Wright, A Sebesteny, A C Hayday, M J Owen

Abstract read
In one paragraph

Article in The American journal of pathology, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 118 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
118citing papers in PubMed, 1 pooled it
8.9field-weighted citation impact, top 2% 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

118 citing papers in PubMed, 1 synthesis or guideline pooled it, 339 citations in OpenAlex.

  1. Pooled it
  2. Ion transport and epithelial barrier dysfunction in experimental models of ulcerative colitis.American journal of physiology. Gastrointestinal and liver physiology · 2025
    Review
  3. Review
  4. Early subclinical stages of the inflammatory bowel diseases: insights from human and animal studies.American journal of physiology. Gastrointestinal and liver physiology · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. iScience · 2022
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. The microbiome and rodent models of immune mediated diseases.Mammalian genome : official journal of the International Mammalian Genome Society · 2021
    Review
  19. Article
  20. Review

58 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

6 authors at 1 institution in 1 country.

L DiandaImperial Cancer Research Fund, London, United Kingdom.
A M Hanby
N A Wright
A Sebesteny
A C Hayday
M J Owen
The Honourable Society of Lincoln's Inn · GB

Funding

SPECIFICITY DISTRIBUTION/FUNCTION OF GAMMA DELTA T-CELLSR01AI027855 · NIAID · YALE UNIVERSITY · PI TIGELAAR, ROBERT E. · 1989 to 2000
$322k
ALPHA BETA T CELL INDEPENDENT B CELL FUNCTIONR01AI038932 · NIAID · YALE UNIVERSITY · PI HAYDAY, ADRIAN CLIVE · 1996 to 2000
$245k
NIAID NIH HHS AI27855NIAID NIH HHS AI38932
6 · The paper itself

Abstract

Mice with null mutations in cytokine or T cell receptor (TCR) genes develop intestinal inflammation. In the case of interleukin-2-/- and interleukin-10-/- mice it has been demonstrated that normal intestinal bacterial flora can cause gut pathology. TCR-alpha-/- mice not only develop colitis but also produce a strong antibody response to self-antigens, such as double-stranded DNA. It is therefore important to establish whether the intestinal inflammation develops spontaneously or is induced by luminal antigens. To address this issue, a germ-free colony of TCR-alpha-/- mice was derived and compared with TCR-alpha-/- mice kept in conventional specific-pathogen-free conditions. Although specific-pathogen-free animals developed colitis with a high level of penetrance, there was no evidence of intestinal pathology in germ-free animals. Furthermore, intestinal inflammation was not seen in TCR-alpha-/- mice colonized with a limited bacterial flora consisting of Lactobacillus plantarum, Streptococcus faecalis, S. faecium, and/or Escherichia coli. We conclude that intestinal inflammation in TCR-alpha-/- mice does not occur spontaneously nor does it result from the presence of bacteria, per se, but rather it is initiated by a specific organism or group of organisms normally present in the gut flora that have yet to be identified.

Indexed as

AnimalsColitisDisease SusceptibilityGerm-Free LifeMiceMice, Mutant StrainsReceptors, Antigen, T-Cell, alpha-betaSpecific Pathogen-Free OrganismsReceptors, Antigen, T-Cell, alpha-beta

Identifiers

PMID9006326
PMCPMC1858528
OpenAlexW1536547862

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.