Evidence map›Paper›PMID 20720210›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2010

Mucosal anti-CD3 monoclonal antibody attenuates collagen-induced arthritis that is associated with induction of LAP+ regulatory T cells and is enhanced by administration of an emulsome-based Th2-skewing adjuvant.

Henry Yim Wu, Ruth Maron, Ann-Marcia Tukpah, Howard L Weiner

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01287195 (Oral Anti-CD3 for the Treatment of Active Ulcerative Colitis), which is not on this map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.2field-weighted citation impact, top 23% 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.

NCT01287195 phase1 / phase2completednot on this mapstarted 2011, after this paper: background citation

Oral Anti-CD3 for the Treatment of Active Ulcerative Colitis

TypeinterventionalSponsorBrigham and Women's HospitalRan2011 to 2013Enrolled6ConditionsUlcerative ColitisArmsOral OKT3, Omeprazole
3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 50 citations in OpenAlex.

  1. Nasal administration of anti-CD3 mAb (Foralumab) downregulatesProceedings of the National Academy of Sciences of the United States of America · 2023
    Trial
  2. Trial
  3. Trial
  4. Nasal administration of anti-CD3 monoclonal antibody ameliorates disease in a mouse model of Alzheimer's disease.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  5. Article
  6. Article
  7. Hsp65-ProducingFrontiers in immunology · 2020
    Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. LAPExperimental and therapeutic medicine · 2018
    Article
  13. Article
  14. Frontiers in pediatrics · 2018
    Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Your nose knows how to target brain inflammation.Brain : a journal of neurology · 2016
    Article
  20. Review
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

4 authors at 2 institutions in 1 country.

Henry Yim WuBrigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA.
Ruth Maron
Ann-Marcia Tukpah
Howard L Weiner
Harvard University · USBrigham and Women's Hospital · US

Funding

The function of T Bet in EAEP01NS038037 · NINDS · BRIGHAM AND WOMEN'S HOSPITAL · PI WEINER, HOWARD L · 2000 to 2010
$12.8M
MECHANISMS OF THE INDUCTION OF ORAL TOLERANCER01AI043458 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI WEINER, HOWARD L · 1998 to 2015
$5.0M
NIAID NIH HHS AI435801NIAID NIH HHS R01 AI043458NINDS NIH HHS NS38037NINDS NIH HHS P01 NS038037
6 · The paper itself

Abstract

Mucosal (nasal or oral) administration of anti-CD3 mAb is effective in ameliorating animal models of autoimmunity (experimental autoimmune encephalomyelitis, diabetes, and lupus) by inducing LAP(+) regulatory T cells. We tested this approach in an arthritis model using type II collagen. We found that nasal anti-CD3 was more effective than oral anti-CD3 in attenuating the development of arthritis. Nasal anti-CD3 induced a LAP(+) regulatory T cell that secreted high levels of IL-10 and suppressed collagen-specific T cell proliferation and anti-collagen Ab production. However, neither nasal nor oral anti-CD3 attenuated disease when given to animals with ongoing arthritis, and this was associated with a lack of induction of LAP(+) regulatory T cells. We found, however, that coadministration of a novel emulsome adjuvant, which enhances Th2 responses, resulted in the induction of LAP(+) regulatory T cells and suppression of ongoing arthritis by both nasal and oral anti-CD3. Suppression of arthritis by mucosal anti-CD3 was associated with less joint damage, a decrease of TNF-alpha and IFN-gamma mRNA expression in joints, and a reduction in anti-collagen Abs. These results demonstrate that mucosal anti-CD3 therapy may serve as a therapeutic approach in arthritis and that the biologic effect is enhanced by an emulsome-based adjuvant.

Indexed as

Adjuvants, ImmunologicAnimalsAntibodies, MonoclonalArthritis, ExperimentalCD3 ComplexCell DifferentiationCells, CulturedCollagen Type IIEmulsionsMaleMiceMice, Inbred DBAMouth MucosaNasal MucosaPeptidesProtein PrecursorsAdjuvants, ImmunologicAntibodies, MonoclonalCD3 ComplexCollagen Type IIEmulsionslatency-associated propeptide, TGF-betaPeptidesProtein PrecursorsTransforming Growth Factor beta

Identifiers

PMID20720210
PMCPMC2962584
OpenAlexW1557823695

What OpenQuestion holds

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LicenceTDM
Read underepoch 390

Registered trials

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.