Evidence map›Paper›PMID 11698428›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2001

Regulation of IFN-gamma signaling is essential for the cytotoxic activity of CD8(+) T cells.

G Z Tau, S N Cowan, J Weisburg, N S Braunstein, P B Rothman

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
0.5field-weighted citation impact, top 40% 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

58 citing papers in PubMed, 101 citations in OpenAlex.

  1. Article
  2. Review
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  4. Intratumoral delivery of 4-1BBL boosts IL-12-triggered anti-glioma immunity.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
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  5. Nanomaterials Trigger Functional Anti-Tumoral Responses in Primary Human Immune Cells.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  6. Review
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  9. Review
  10. Review
  11. Review
  12. Article
  13. Evolutionary trajectories of immune escape across cancers.bioRxiv : the preprint server for biology · 2025
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Building a novel TRUCK by harnessing the endogenous IFN-gamma promoter for cytokine expression.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  19. Targeting cytokine and chemokine signaling pathways for cancer therapy.Signal transduction and targeted therapy · 2024
    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

5 authors at 1 institution in 1 country.

G Z TauIntegrated Program in Cell, Molecular, and Biophysical Studies, Department of Medicine, College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA.
S N Cowan
J Weisburg
N S Braunstein
P B Rothman
Columbia University · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007367 · NIGMS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI REINER, STEVEN L · 1985 to 2021
$25.1M
SDF1 IN MESENCHYMAL ALTERATIONS OF IMMUNE INJURYP01AI039675 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI JIANG, HONG · 1996 to 1999
–
NIAID NIH HHS P01AI39675NIGMS NIH HHS T32 GM007367
6 · The paper itself

Abstract

Previous studies have demonstrated that, as naive murine CD4(+) cells differentiate into Th1 cells, they lose expression of the second chain of IFN-gammaR (IFN-gammaR2). Hence, the IFN-gamma-producing subset of Th cells is unresponsive to IFN-gamma. Analysis of IFN-gamma-producing CD8(+) T cells demonstrates that, like Th1 cells, these cells do not express IFN-gammaR2. To define the importance of IFN-gamma signaling for the development of functional CD8(+) T cells, mice either lacking IFN-gammaR2 or overexpressing this protein were examined. While CD8(+) T cell development and function appear normal in IFN-gammaR2(-/-) mice, CD8(+) T cell function in IFN-gammaR2 transgenic is altered. IFN-gammaR2 transgenic CD8(+) T cells are unable to lyse target cells in vitro. However, these cells produce Fas ligand, perforin, and granzyme B, the effector molecules required for killing. Interestingly, TG CD8(+) T cells proliferate normally and produce cytokines, such as IFN-gamma in response to antigenic stimulation. Therefore, although IFN-gamma signaling is not required for the generation of normal cytotoxic T cells, constitutive IFN-gamma signaling can selectively impair the cytotoxic function of CD8(+) T cells.

Indexed as

Cytotoxicity, ImmunologicSignal TransductionAnimalsCell LineCells, CulturedClone CellsCytokinesCytotoxicity Tests, ImmunologicImmunologic MemoryInterferon-gammaInterferon gamma ReceptorLymphocyte ActivationMiceMice, KnockoutMice, TransgenicReceptors, InterferonCytokinesInterferon-gammaInterferon gamma ReceptorReceptors, InterferonRNA, Messenger

Identifiers

PMID11698428
PMCPMC4416493
OpenAlexW1606264375

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.