Evidence map›Paper›PMID 19505881›Full record

ArticleGut2009

Anti-CTLA-4 treatment induces IL-10-producing ICOS+ regulatory T cells displaying IDO-dependent anti-inflammatory properties in a mouse model of colitis.

C Coquerelle, G Oldenhove, V Acolty, J Denoeud, G Vansanten, J-M Verdebout, A Mellor, J A Bluestone, M Moser

Open access · greenAbstract read
In one paragraph

Article in Gut, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.6field-weighted citation impact, top 12% 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

35 citing papers in PubMed, 72 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. ICOSFrontiers in immunology · 2020
    Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Review
  16. The Anti-Inflammatory Effects of Vitamin D in Tumorigenesis.International journal of molecular sciences · 2018
    Review
  17. Anti-Inducible Costimulator Monoclonal Antibody Treatment of Canine Chronic Graft-versus-Host Disease.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2018
    Article
  18. Review
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 2 countries.

C CoquerelleDépartement de Biologie Moléculaire, Laboratoire de Physiologie Animale, Université Libre de Bruxelles, Rue des Pr Jeener et Brachet, 12, 6041 Gosselies, Belgium.
G Oldenhove
V Acolty
J Denoeud
G Vansanten
J-M Verdebout
A Mellor
J A Bluestone
M Moser
Université Libre de Bruxelles · BEInfectious Disease Consultants · USInstitute of Pathology and Genetics · BEUniversity of California, San Francisco · US

Funding

Src tyrosine kinases and autoimmunity.P01AI035297 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BLUESTONE, JEFFREY A · 1993 to 2010
$16.5M
NIAID NIH HHS P01 AI035297
6 · The paper itself

Abstract

BACKGROUND AND

aimsCytotoxic T lymphocyte-associated antigen 4 (CTLA-4) has been shown to act as a negative regulator of T cell function and has been implicated in the regulation of T helper 1 (Th1)/Th2 development and the function of regulatory T cells. Tests were carried out to determine whether anti-CTLA-4 treatment would alter the polarisation of naive T cells in vivo.

methodsMice were treated with anti-CTLA-4 monoclonal antibody (mAb) (UC10-4F10) at the time of immunisation or colonic instillation of trinitrobenzene sulfonic acid (TNBS). The cytokines produced by lymph node cells after in vitro antigenic stimulation and the role of indoleamine 2,3 dioxygenase (IDO) and of interleukin-10 (IL-10) were tested, and the survival of mice was monitored.

resultsInjection of anti-CTLA-4 mAb in mice during priming induced the development of adaptive CD4(+) regulatory T cells which expressed high levels of ICOS (inducible co-stimulator), secreted IL-4 and IL-10. This treatment inhibited Th1 memory responses in vivo and repressed experimental intestinal inflammation. The anti-CTLA-4-induced amelioration of disease correlated with IDO expression and infiltration of ICOS(high) Foxp3(+) T cells in the intestine, suggesting that anti-CTLA-4 acted indirectly through the development of regulatory T cells producing IL-10 and inducing IDO.

conclusionsThese observations emphasise the synergy between IL-10 and IDO as anti-inflammatory agents and highlight anti-CTLA-4 treatment as a potential novel immunotherapeutic approach for inducing adaptive regulatory T cells.

Indexed as

AnimalsAntibodies, MonoclonalAntigens, CDColitisCTLA-4 AntigenIndoleamine-Pyrrole 2,3,-DioxygenaseInterleukin-10Intestinal MucosaMiceMice, Inbred BALB CMice, Inbred C57BLT-Lymphocytes, RegulatoryTrinitrobenzenesulfonic AcidAntibodies, MonoclonalAntigens, CDCTLA-4 AntigenCtla4 protein, mouseIndoleamine-Pyrrole 2,3,-DioxygenaseInterleukin-10Trinitrobenzenesulfonic Acid

Identifiers

PMID19505881
PMCPMC2917097
OpenAlexW2005956916

What OpenQuestion holds

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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.