Evidence map›Paper›PMID 9802977›Full record

ArticleThe Journal of experimental medicine1998

Interferon gamma derived from CD4(+) T cells is sufficient to mediate T helper cell type 1 development.

A E Wakil, Z E Wang, J C Ryan, D J Fowell, R M Locksley

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

36 citing papers in PubMed, 96 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. The transcription factor Zfp281 sustains CD4Cellular & molecular immunology · 2020
    Article
  11. Article
  12. Modes of Communication between T Cells and Relevance for Immune Responses.International journal of molecular sciences · 2020
    Review
  13. Article
  14. Review
  15. mTORC2 deficiency in cutaneous dendritic cells potentiates CD8American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2019
    Article
  16. Paracrine costimulation of IFN-γ signaling by integrins modulates CD8 T cell differentiation.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  17. Article
  18. Cytotoxic activity in cutaneous leishmaniasis.Memorias do Instituto Oswaldo Cruz · 2017
    Review
  19. Article
  20. Cutaneous Manifestations of Human and Murine Leishmaniasis.International journal of molecular sciences · 2017
    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

5 authors at 3 institutions in 1 country.

A E WakilDepartment of Medicine and the Department of Microbiology/Immunology, University of California San Francisco, San Francisco, California 94143, USA.
Z E Wang
J C Ryan
D J Fowell
R M Locksley
Howard Hughes Medical Institute · USUnited States Department of Veterans Affairs · USUniversity of California, San Francisco · US

Funding

Parasite immunity orchestrated by type 2 immune cellsR01AI026918 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LOCKSLEY, RICHARD M · 1988 to 2022
$3.8M
Parasite Immunity Orchestrated by Th2 CellsR37AI026918 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LOCKSLEY, RICHARD M · 2006 to 2015
$3.8M
NIAID NIH HHS AI26918NIAID NIH HHS R01 AI026918NIAID NIH HHS R37 AI026918
6 · The paper itself

Abstract

Interferon gamma (IFN-gamma) has been implicated in T helper type 1 (Th1) cell development through its ability to optimize interleukin 12 (IL-12) production from macrophages and IL-12 receptor expression on activated T cells. Various systems have suggested a role for IFN-gamma derived from the innate immune system, particularly natural killer (NK) cells, in mediating Th1 differentiation in vivo. We tested this requirement by reconstituting T cell and IFN-gamma doubly deficient mice with wild-type CD4(+) T cells and challenging the mice with pathogens that elicited either minimal or robust IL-12 in vivo (Leishmania major or Listeria monocytogenes, respectively). Th1 cells developed under both conditions, and this was unaffected by the presence or absence of IFN-gamma in non-T cells. Reconstitution with IFN-gamma-deficient CD4(+) T cells could not reestablish control over L. major, even in the presence of IFN-gamma from the NK compartment. These data demonstrate that activated T cells can maintain responsiveness to IL-12 through elaboration of endogenous IFN-gamma without requirement for an exogenous source of this cytokine.

Indexed as

AnimalsCD4-Positive T-LymphocytesCell DifferentiationInterferon-gammaInterleukin-12Killer Cells, NaturalLeishmania majorLeishmaniasis, CutaneousListeria monocytogenesMiceMice, Inbred C57BLMice, KnockoutTh1 CellsInterferon-gammaInterleukin-12

Identifiers

PMID9802977
PMCPMC2212510
OpenAlexW2019993326

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.