Evidence map›Paper›PMID 22017431›Full record

ReviewImmunological reviews2011

Roles of tumor necrosis factor receptor associated factor 3 (TRAF3) and TRAF5 in immune cell functions.

Joanne M Hildebrand, Zuoan Yi, Claire M Buchta, Jayakumar Poovassery, Laura L Stunz, Gail A Bishop

Open access · greenAbstract readReview
In one paragraph

Review in Immunological reviews, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

59 citing papers in PubMed, 105 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. METTL3-mediated mThe Kaohsiung journal of medical sciences · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
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  18. Targeted deep sequencing of gastric marginal zone lymphoma identified alterations of TRAF3 and TNFAIP3 that were mutually exclusive for MALT1 rearrangement.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2018
    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

6 authors at 1 institution in 1 country.

Joanne M HildebrandDepartment of Microbiology, The University of Iowa, Iowa City, IA 52242, USA.
Zuoan Yi
Claire M Buchta
Jayakumar Poovassery
Laura L Stunz
Gail A Bishop
University of Iowa · US

Funding

PREDOCTORAL TRAINING PROGRAM IN IMMUNOLOGYT32AI007485 · NIAID · UNIVERSITY OF IOWA · PI Kevin L Legge · 1995 to 2026
$5.4M
Mechanisms of Alteration of B Lymphocyte Function by LMP1R01CA099997 · NCI · UNIVERSITY OF IOWA · PI BISHOP, GAIL A. · 2003 to 2013
$3.2M
The Roles of TRAF3 in Lymphocyte SignalingR01AI028847 · NIAID · UNIVERSITY OF IOWA · PI BISHOP, GAIL A. · 1996 to 2011
$3.1M
TRAFs and Rafts in CD40 Signaling to B LymphocytesR01AI049993 · NIAID · UNIVERSITY OF IOWA · PI BISHOP, GAIL A. · 2001 to 2009
$2.7M
Regulation of lymphocyte receptor signaling by TRAF interactionsR56AI049993 · NIAID · UNIVERSITY OF IOWA · PI BISHOP, GAIL A. · 2010 to 2010
$374k
Understanding TRAF3-mediated regulation of T lymphocyte functionsR56AI028847 · NIAID · UNIVERSITY OF IOWA · PI BISHOP, GAIL A. · 2013 to 2013
$227k
REGULATION OF CLASS II--MEDIATED B CELL DIFFERENTIATIONR29AI028847 · NIAID · UNIVERSITY OF IOWA · PI BISHOP, GAIL A. · 1990 to 1994
–
NCI NIH HHS CA099997NCI NIH HHS R01 CA099997NIAID NIH HHS AI28847NIAID NIH HHS AI49993NIAID NIH HHS R01 AI028847NIAID NIH HHS R01 AI049993NIAID NIH HHS R56 AI028847NIAID NIH HHS R56 AI049993NIAID NIH HHS T32 AI007485
6 · The paper itself

Abstract

A large and diverse group of receptors utilizes the family of cytoplasmic signaling proteins known as tumor necrosis factor receptor (TNFR)-associated factors (TRAFs). In recent years, there has been a resurgence of interest and exploration of the roles played by TRAF3 and TRAF5 in cellular regulation, particularly in cells of the immune system, the cell types of focus in this review. This work has revealed that TRAF3 and TRAF5 can play diverse roles for different receptors even in the same cell type, as well as distinct roles in different cell types. Evidence indicates that TRAF3 and TRAF5 play important roles beyond the TNFR-superfamily (SF) and viral mimics of its members, mediating certain innate immune receptor and cytokine receptor signals, and most recently, signals delivered by the T-cell receptor (TCR) signaling complex. Additionally, much research has demonstrated the importance of TRAF3-mediated cellular regulation via its cytoplasmic interactions with additional signaling proteins. In particular, we discuss below evidence for the participation by TRAF3 in a number of the regulatory post-translational modifications involving ubiquitin that are important in various signaling pathways.

Indexed as

Immunity, InnateAnimalsB-LymphocytesCell SurvivalGene ExpressionHumansMiceMice, KnockoutMyeloid CellsNF-kappa BProtein BindingProtein Processing, Post-TranslationalReceptors, Tumor Necrosis FactorSignal TransductionT-LymphocytesTNF Receptor-Associated Factor 3NF-kappa BReceptors, Tumor Necrosis FactorTNF Receptor-Associated Factor 3TNF Receptor-Associated Factor 5Tumor Necrosis Factor-alphaUbiquitin

Identifiers

PMID22017431
PMCPMC3202299
OpenAlexW1583006772

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.