Evidence map›Paper›PMID 19017969›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2008

TNF receptor-associated factor 5 is required for optimal T cell expansion and survival in response to infection.

Zachary J Kraus, Jodie S Haring, Gail A Bishop

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

21 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. TRAF5 negatively regulates TLR signaling in B lymphocytes.Journal of immunology (Baltimore, Md. : 1950) · 2014
    Article
  14. Article
  15. Notch controls the magnitude of T helper cell responses by promoting cellular longevity.Proceedings of the National Academy of Sciences of the United States of America · 2012
    Article
  16. Article
  17. Review
  18. Article
  19. Article
  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

3 authors at 3 institutions in 3 countries.

Zachary J KrausGraduate Program in Immunology, University of Iowa, Iowa City, IA 52242, USA.
Jodie S Haring
Gail A Bishop
Czech Academy of Sciences, Institute of Microbiology · CZInstitute of Immunology · HRUniversity of Iowa · US

Funding

TRAFs and Rafts in CD40 Signaling to B LymphocytesR01AI049993 · NIAID · UNIVERSITY OF IOWA · PI BISHOP, GAIL A. · 2001 to 2009
$2.7M
NIAID NIH HHS R01 AI049993
6 · The paper itself

Abstract

Receptors belonging to the TNF-receptor (TNF-R) superfamily include important costimulatory molecules, many of which specifically affect T cell activation. TNF receptor-associated factors (TRAFs) are recruited to many TNF-R superfamily members and are important modulators of the proximal signaling events that occur at the time of receptor engagement and activation. TRAF5 has been shown to be a positive regulator of a number of these receptors that are involved in T cell costimulation. However, the potential importance of TRAF5 in cellular immune responses to infection or in T cell expansion and memory have not been studied. We report in this study that TRAF5 was required for optimal CD8(+) T cell responses following infection with Listeria monocytogenes expressing OVA (LM-OVA). TRAF5 was necessary for optimal T cell expansion following primary infection with LM-OVA, and its absence resulted in fewer memory CD8(+) T cells following LM-OVA infection, together with higher bacterial loads in the liver. The effect of TRAF5 on CD8(+) T cell expansion was T cell intrinsic and not due to effects of TRAF5 deficiency on APCs. Although their proliferative ability remained intact, CD8(+) T cells from TRAF5(-/-) mice were more sensitive to apoptosis and were unresponsive to the prosurvival effects of the TNF-R superfamily costimulator CD27. Collectively, these studies identify TRAF5 as an important positive signaling element that enhances T cell expansion and pathogen containment by providing a survival advantage to responding Ag-specific CD8(+) T cells during infection.

Indexed as

Cell ProliferationLymphocyte ActivationAnimalsAntigens, BacterialApoptosisCD8-Positive T-LymphocytesCell SurvivalListeria monocytogenesListeriosisLiverMiceMice, KnockoutTNF Receptor-Associated Factor 5Tumor Necrosis Factor Receptor Superfamily, Member 7Antigens, BacterialTNF Receptor-Associated Factor 5Tumor Necrosis Factor Receptor Superfamily, Member 7

Identifiers

PMID19017969
PMCPMC2636746
OpenAlexW2149717963

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.