Evidence map›Paper›PMID 7751026›Full record

ArticleImmunology1995

The role of interleukin-12 in acquired immunity to Mycobacterium tuberculosis infection.

A M Cooper, A D Roberts, E R Rhoades, J E Callahan, D M Getzy, I M Orme

Open access · greenAbstract read
In one paragraph

Article in Immunology, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 116 papers.

0numbers the graph read from it
0cells of the map it votes in
116citing papers in PubMed
18.8field-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

116 citing papers in PubMed, 311 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. The Effect of Orally Administered Multi-Strain Probiotic Formulation (International journal of molecular sciences · 2024
    Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Antibiotic Resistance toAntibiotics (Basel, Switzerland) · 2022
    Review
  10. Article
  11. Article
  12. Review
  13. Type I interferons in tuberculosis: Foe and occasionally friend.The Journal of experimental medicine · 2018
    Review
  14. Article
  15. Striking the right immunological balance prevents progression of tuberculosis.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2017
    Review
  16. Article
  17. Article
  18. T Cell-Derived IL-10 Impairs Host Resistance toJournal of immunology (Baltimore, Md. : 1950) · 2017
    Article
  19. Article
  20. Review

56 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.

A M CooperDepartment of Microbiology, Colorado State University, Fort Collins 80523, USA.
A D Roberts
E R Rhoades
J E Callahan
D M Getzy
I M Orme
Colorado State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The early phase of acquired cellular immunity to Mycobacterium tuberculosis infection is mediated by the emergence of protective CD4 T lymphocytes that secrete cytokines including interferon-gamma (IFN-gamma), a molecule which is pivotal in the expression of resistance to tuberculosis. Recent evidence demonstrates that infection with M. tuberculosis induces peripheral blood mononuclear cells to release the cytokine interleukin-12 (IL-12), a molecule that promotes the emergence of T-helper type-1 (Th1), IFN-gamma-producing T cells. We demonstrate here that IL-12 mRNA expression was induced by M. tuberculosis infection both in vivo and in vitro and that exogenous administration of IL-12 to mice transiently resulted in increased resistance to the infection. IL-12 also increased the production of IFN-gamma by both splenocytes derived from infected animals treated in vivo and by antigen-stimulated CD4 cells from untreated infected animals, with maximal effects at times associated with the expansion of antigen-specific CD4 T cells in vivo. In the absence of a T-cell response, as seen in SCID mice or nude mice, IL-12 only slightly augmented the moderate bacteriostatic capacity of these immunocompromised mice. Neutralization of IL-12 by specific monoclonal antibodies resulted in a reduction in granuloma integrity and slowing of the capacity of the animal to control bacterial growth.

Indexed as

AnimalsFemaleGene ExpressionImmunity, CellularImmunocompromised HostInterferon-gammaInterleukin-12Killer Cells, NaturalLiverMiceMice, Inbred C57BLMice, NudeMice, SCIDMycobacterium tuberculosisRNA, MessengerSpleenInterferon-gammaInterleukin-12RNA, Messenger

Identifiers

PMID7751026
PMCPMC1415123
OpenAlexW101818886

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.