Evidence map›Paper›PMID 25015828›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2014

Antigen-specific naive CD8+ T cells produce a single pulse of IFN-γ in vivo within hours of infection, but without antiviral effect.

Martin P Hosking, Claudia T Flynn, J Lindsay Whitton

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

25 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Cells · 2025
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Group AScience immunology · 2023
    Article
  11. Review
  12. Review
  13. Oncolytic adenovirus decreases the proportion of TIM-3Journal for immunotherapy of cancer · 2022
    Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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
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

3 authors at 1 institution in 1 country.

Martin P HoskingDepartment of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA 92037 mhosking@scripps.edu.
Claudia T FlynnDepartment of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA 92037.
J Lindsay WhittonDepartment of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA 92037.
Scripps Research Institute · US

Funding

BLOOD SYSTEMS IN COAGULATION AND VESSEL DISEASET32HL007195 · NHLBI · SCRIPPS RESEARCH INSTITUTE, THE · PI RUF, WOLFRAM · 1985 to 2011
$5.1M
Functional Analyses of Antiviral CD4+ T Cell ResponsesR01AI052351 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI WHITTON, J. LINDSAY · 2003 to 2013
$3.9M
Understanding and manipulating the T cell contraction phaseR01AI077607 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI WHITTON, J. LINDSAY · 2008 to 2012
$2.3M
Functional analyses of antiviral CD4+ T cell responsesR21AI052351 · NIAID · SCRIPPS RESEARCH INSTITUTE · PI WHITTON, J. LINDSAY · 2002 to 2002
$370k
NHLBI NIH HHS T32 HL007195NHLBI NIH HHS T32 HL007195-34NIAID NIH HHS AI052351NIAID NIH HHS AI077607NIAID NIH HHS R01 AI052351NIAID NIH HHS R01 AI077607NIAID NIH HHS R21 AI052351
6 · The paper itself

Abstract

In vitro studies have shown that naive CD8(+) T cells are unable to express most of their effector proteins until after at least one round of cell division has taken place. We have reassessed this issue in vivo and find that naive CD8(+) T cells mount Ag-specific responses within hours of infection, before proliferation has commenced. Newly activated naive Ag-specific CD8(+) T cells produce a rapid pulse of IFN-γ in vivo and begin to accumulate granzyme B and perforin. Later, in vivo cytolytic activity is detectable, coincident with the initiation of cell division. Despite the rapid development of these functional attributes, no antiviral effect was observed early during infection, even when the cells are present in numbers similar to those of virus-specific memory cells. The evolutionary reason for the pulse of IFN-γ synthesis by naive T cells is uncertain, but the lack of antiviral impact suggests that it may be regulatory.

Indexed as

Adoptive TransferAnimalsCD8-Positive T-LymphocytesCell DifferentiationCell DivisionGranzymesImmunologic MemoryInterferon-gammaLymphocyte ActivationLymphocytic ChoriomeningitisLymphocytic choriomeningitis virusMiceMice, Inbred C57BLMice, TransgenicPerforinT-bet Transcription FactorEomes protein, mouseGranzymesInterferon-gammaPerforinT-bet Transcription FactorT-Box Domain ProteinsTumor Necrosis Factor-alpha

Identifiers

PMID25015828
PMCPMC4119517
OpenAlexW2149749056

What OpenQuestion holds

Textmetadata
LicenceTDM
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.