Evidence map›Paper›PMID 19264470›Full record

ReviewCurrent opinion in immunology2009

The diversity of costimulatory and inhibitory receptor pathways and the regulation of antiviral T cell responses.

Alison Crawford, E John Wherry

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in immunology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

80 citing papers in PubMed, 141 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Myeloid-Derived Suppressor Cells Induce Exhaustion-Like CD8International journal of biological sciences · 2024
    Article
  5. Review
  6. The role of CD4MedComm · 2023
    Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. The roadmap towards cure of chronic hepatitis B virus infection.Journal of the Royal Society of New Zealand · 2022
    Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. Platelet Induced Functional Alteration of CD4International journal of molecular sciences · 2020
    Article
  19. Article
  20. Article

20 more citing papers are in PubMed but not listed here.

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.

Alison CrawfordImmunology Program, The Wistar Institute, Philadelphia, PA 19104, USA.
E John Wherry
The Wistar Institute · US

Funding

Virology CoreU19AI082630 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI RAYMOND T CHUNG, GEORG Michael LAUER · 2009 to 2026
$48.1M
Visualizing Effects of Costimulation on Antiviral ImmunityP01AI078897 · NIAID · HARVARD MEDICAL SCHOOL · PI VON ANDRIAN, ULRICH H · 2008 to 2012
$12.1M
The Impact of Bacterial Co-Infectin on Respiratory Virus-Specific T cell ResponseU19AI083022 · NIAID · WISTAR INSTITUTE · PI SHEN, HAO · 2009 to 2013
$10.7M
Regulation of exhaustion and altered CD8 T cell memory during chronic InfectionR01AI071309 · NIAID · WISTAR INSTITUTE · PI WHERRY, E. JOHN · 2006 to 2010
$1.8M
Memory CD8 T cell subset cooperation via chemokines in protective immunity to infR21AI077098 · NIAID · WISTAR INSTITUTE · PI WHERRY, E. JOHN · 2007 to 2008
$427k
NIAID NIH HHS AI071309NIAID NIH HHS AI077098NIAID NIH HHS P01 AI078897NIAID NIH HHS R01 AI071309NIAID NIH HHS R21 AI077098NIAID NIH HHS U19 AI082630NIAID NIH HHS U19 AI083022PHS HHS HHSN26620050030C
6 · The paper itself

Abstract

T cell responses are regulated by integrating positive and negative signals from costimulatory and inhibitory receptors. While the function of specific T cell costimulatory molecules during infections has been appreciated for some time, recent observations have now revealed a crucial role for inhibitory receptors in regulating T cell responses to pathogens, especially during chronic infections. A key emerging principle is that there is considerable diversity in the number and type of inhibitory receptors that can be expressed by T cells during both acute and chronic infections. These distinct inhibitory pathways appear to cooperate in regulating T cell function, could have distinct mechanisms of action, and are likely to provide novel therapeutic targets during persisting infections and other diseases.

Indexed as

AnimalsCD28 AntigensHumansLymphocyte ActivationModels, ImmunologicalReceptors, ImmunologicSignal TransductionT-LymphocytesTumor Necrosis Factor Receptor Superfamily, Member 7Virus DiseasesCD28 AntigensReceptors, ImmunologicTumor Necrosis Factor Receptor Superfamily, Member 7

Identifiers

PMID19264470
PMCPMC2720162
OpenAlexW2016909108

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.