Evidence map›Paper›PMID 15606800›Full record

ArticleImmunology2005

Influence of pathological progression on the balance between cellular and humoral immune responses in bovine tuberculosis.

Michael D Welsh, Rodat T Cunningham, David M Corbett, R Martyn Girvin, James McNair, Robin A Skuce, David G Bryson, John M Pollock

Open access · greenAbstract read
In one paragraph

Article in Immunology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed, 1 pooled it
4.5field-weighted citation impact, top 5% 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

70 citing papers in PubMed, 1 synthesis or guideline pooled it, 190 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Congenital Tuberculosis in a Stillborn Calf.Pathogens (Basel, Switzerland) · 2026
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. B Cell and Antibody Responses in Bovine Tuberculosis.Antibodies (Basel, Switzerland) · 2024
    Review
  10. Article
  11. Article
  12. Detection ofFrontiers in microbiology · 2024
    Article
  13. Article
  14. Limited usefulness of the ISFrontiers in veterinary science · 2024
    Article
  15. Article
  16. The combination ofFrontiers in immunology · 2024
    Article
  17. Review
  18. Article
  19. "Spotting"Frontiers in immunology · 2023
    Article
  20. Article

10 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

8 authors at 2 institutions in 1 country.

Michael D WelshVeterinary Sciences Division, The Department of Agriculture and Rural Development, Stoney Road, Stormont, Belfast, BT4 3SD, UK. michael.welsh@dardni.gov.uk
Rodat T Cunningham
David M Corbett
R Martyn Girvin
James McNair
Robin A Skuce
David G Bryson
John M Pollock
Department of Agriculture and Rural Development · GBQueen's University Belfast · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Studies of tuberculosis have suggested a shift in dominance from a T helper type 1 (Th1) towards a Th2 immune response that is associated with suppressed cell-mediated immune (CMI) responses and increased humoral responses as the disease progresses. In this study a natural host disease model was used to investigate the balance of the evolving immune response towards Mycobacterium bovis infection in cattle with respect to pathogenesis. Cytokine analysis of CD4 T-cell clones derived from M. bovis-infected animals gave some indication that there was a possible relationship between enhanced pathogenesis and an increased ratio of Th0 [interleukin-4-positive/interferon-gamma-positive (IL-4(+)/IFN-gamma(+))] clones to Th1 (IFN-gamma(+)) clones. All animals developed strong antimycobacterial CMI responses, but depressed cellular responses were evident as the disease progressed, with the IFN-gamma test failing to give consistently positive results in the latter stages. Furthermore, a stronger Th0 immune bias, depressed in vitro CMI responses, elevated levels of IL-10 expression and enhanced humoral responses were also associated with increased pathology. In minimal disease, however, a strong Th1 immune bias was maintained and an anti-M. bovis humoral response failed to develop. It was also seen that the level of the anti-M. bovis immunoglobulin G1 (IgG1) isotype antibody responses correlated with the pathology scores, whereas CMI responses did not have as strong a relationship with the development of pathology. Therefore, the development and maintenance of a Th1 IFN-gamma response is associated with a greater control of M. bovis infection. Animals progressing from a Th1-biased to a Th0-biased immune response developed more extensive pathology and performed less well in CMI-based diagnostic tests but developed strong IgG1 humoral responses.

Indexed as

AnimalsAntigens, BacterialCattleCell DivisionCells, CulturedClone CellsCytokinesCytotoxicity, ImmunologicDisease ProgressionHypersensitivity, DelayedImmunity, CellularImmunoglobulin GImmunoglobulin IsotypesInterferon-gammaLymphocyte ActivationMaleAntigens, BacterialCytokinesImmunoglobulin GImmunoglobulin IsotypesInterferon-gammaRNA, MessengerTuberculin

Identifiers

PMID15606800
PMCPMC1782060
OpenAlexW2094495174

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.