Evidence map›Paper›PMID 22116087›Full record

ArticleNature reviews. Immunology2011

The emerging role of CTLA4 as a cell-extrinsic regulator of T cell responses.

Lucy S K Walker, David M Sansom

Abstract read
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In one paragraph

Article in Nature reviews. Immunology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 430 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
430citing papers in PubMed, 3 pooled it
–field-weighted citation impact
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

430 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Review
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  7. Review
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  9. Review
  10. CTLA-4: a promising immunosuppressive immune checkpoint in prostate cancer therapy.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Current oncology (Toronto, Ont.) · 2026
    Review
  17. Article
  18. Immune checkpoint molecules beyond PD-1 and CTLA-4: emerging targets in autoimmune diseases and cancer immunotherapy.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Review
  19. Review
  20. Article

370 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.

Lucy S K WalkerMRC Centre for Immune Regulation, University of Birmingham Medical School, Birmingham, UK. L.S.Walker@bham.ac.uk
David M Sansom

Funding

Biotechnology and Biological Sciences Research Council BB/H013598/1Medical Research Council G0802382
6 · The paper itself

Abstract

The T cell protein cytotoxic T lymphocyte antigen 4 (CTLA4) was identified as a crucial negative regulator of the immune system over 15 years ago, but its mechanisms of action are still under debate. It has long been suggested that CTLA4 transmits an inhibitory signal to the cells that express it. However, not all the available data fit with a cell-intrinsic function for CTLA4, and other studies have suggested that CTLA4 functions in a T cell-extrinsic manner. Here, we discuss the data for and against the T cell-intrinsic and -extrinsic functions of CTLA4.

Indexed as

AnimalsAntigen PresentationCD28 AntigensCells, CulturedClathrin-Coated VesiclesCTLA-4 AntigenEndocytosisHumansImmune ToleranceIndoleamine-Pyrrole 2,3,-DioxygenaseLymphocyte ActivationMiceMice, Inbred NODMice, KnockoutMice, TransgenicModels, ImmunologicalCD28 AntigensCTLA-4 AntigenCtla4 protein, mouseIndoleamine-Pyrrole 2,3,-DioxygenaseProtein Isoforms

Identifiers

PMID22116087

What OpenQuestion holds

Textmetadata
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.