Evidence map›Paper›PMID 31749173›Full record

ReviewJournal of leukocyte biology2020

TRAF family molecules in T cells: Multiple receptors and functions.

Tina Arkee, Gail A Bishop

Open access · bronzeAbstract readReview
In one paragraph

Review in Journal of leukocyte biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 17% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. A Conserved Planthopper MATH-BTB Protein Regulates Fecundity inInternational journal of molecular sciences · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. TRAF3: Guardian of T lymphocyte functions.Frontiers in immunology · 2023
    Review
  13. Review
  14. Review
  15. K63 ubiquitination in immune signaling.Trends in immunology · 2022
    Review
  16. Review
  17. Article
  18. Article
  19. 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

2 authors at 1 institution in 1 country.

Tina ArkeeGraduate Program in Immunology, The University of Iowa, Iowa City, Iowa, USA.
Gail A BishopGraduate Program in Immunology, The University of Iowa, Iowa City, Iowa, USA.ORCID 0000-0002-1291-5078
University of Iowa · US

Funding

Viral VectorP30CA086862 · NCI · UNIVERSITY OF IOWA · PI Christopher K Laubenthal · 2000 to 2026
$70.0M
Pulmonary Toxicology Facility CoreP30ES005605 · NIEHS · UNIVERSITY OF IOWA · PI Jong Sung Kim · 1990 to 2026
$40.5M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007337 · NIGMS · UNIVERSITY OF IOWA · PI GEYER, PAMELA K., LENTZ, STEVEN R · 1985 to 2020
$15.9M
PROGRAM IN HEMOSTASIS AND THROMBOSIS FOR ACADEMICT32HL007344 · NHLBI · UNIVERSITY OF IOWA · PI Anil Kumar Chauhan, Steven R Lentz · 1985 to 2026
$6.5M
PREDOCTORAL TRAINING PROGRAM IN IMMUNOLOGYT32AI007485 · NIAID · UNIVERSITY OF IOWA · PI Kevin L Legge · 1995 to 2026
$5.4M
Molecular regulation of T cell activation signals by TRAF3R01AI123107 · NIAID · UNIVERSITY OF IOWA · PI BISHOP, GAIL A. · 2016 to 2020
$1.9M
Understanding and applying innate and adaptive immune signal interactionsI01BX001702 · VA · IOWA CITY VA MEDICAL CENTER · PI BISHOP, GAIL A. · 2013 to 2020
–
BLRD VA I01 BX001702NCI NIH HHS P30 CA086862NHLBI NIH HHS T32 HL007344NIAID NIH HHS R01 AI123107NIAID NIH HHS T32 AI007485NIEHS NIH HHS P30 ES005605NIGMS NIH HHS T32 GM007337
6 · The paper itself

Abstract

The TNFR superfamily of receptors, the major focus of the recent TNFR Superfamily Conference held in June 2019, employ the TNFR-associated factor (TRAF) family of adaptor proteins in key aspects of their signaling pathways. Although many early studies investigated TRAF functions via exogenous overexpression in nonhematopoietic cell lines, it has subsequently become clear that whereas TRAFs share some overlap in function, each also plays unique biologic roles, that can be highly context dependent. This brief review summarizes the current state of knowledge of functions of each of the TRAF molecules that mediate important functions in T lymphocytes: TRAFs 1, 2, 3, 5, and 6. Due to our current appreciation of the contextual nature of TRAF function, our focus is upon findings made specifically in T lymphocytes. Key T cell functions for each TRAF are detailed, as well as future knowledge gaps of interest and importance.

Indexed as

AnimalsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesDisease Models, AnimalGene Expression RegulationHumansImmunologic Deficiency SyndromesImmunologic MemoryMiceMice, KnockoutProtein IsoformsReceptors, Tumor Necrosis FactorSignal TransductionTumor Necrosis Factor-alphaTumor Necrosis Factor Receptor-Associated Peptides and ProteinsProtein IsoformsReceptors, Tumor Necrosis FactorTumor Necrosis Factor-alphaTumor Necrosis Factor Receptor-Associated Peptides and Proteinssignal transductionT cellTNFR superfamily

Identifiers

PMID31749173
PMCPMC7239704
OpenAlexW2989611105

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.