Evidence map›Paper›PMID 20890040›Full record

ArticleThe Journal of clinical investigation2010

Therapeutic Treg expansion in mice by TNFRSF25 prevents allergic lung inflammation.

Taylor H Schreiber, Dietlinde Wolf, Matthew S Tsai, Jackie Chirinos, Vadim V Deyev, Louis Gonzalez, Thomas R Malek, Robert B Levy, Eckhard R Podack

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 97 papers.

0numbers the graph read from it
0cells of the map it votes in
97citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

97 citing papers in PubMed, 158 citations in OpenAlex.

  1. Article
  2. Decoding TNF receptor superfamily control of CD4Cell communication and signaling : CCS · 2026
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. TL1A induces apoptosis via DR3 in grass carp (Fish and shellfish immunology reports · 2023
    Article
  14. Endogenous inhibitory mechanisms in asthma.The journal of allergy and clinical immunology. Global · 2023
    Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Taylor H SchreiberSheila and David Fuente Program in Cancer Biology, University of Miami Miller School of Medicine, Miami, Florida 33101, USA.
Dietlinde Wolf
Matthew S Tsai
Jackie Chirinos
Vadim V Deyev
Louis Gonzalez
Thomas R Malek
Robert B Levy
Eckhard R Podack
University of Miami · US

Funding

REGULATION OF ANTI-TUMOR IMMUNITYP01CA109094 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI MALEK, THOMAS R · 2007 to 2011
$6.2M
DR3 in Asthma and in OntogenyR01AI061807 · NIAID · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI PODACK, ECKHARD R · 2004 to 2008
$1.9M
NCI NIH HHS NCI-5PO1CA109094-03NCI NIH HHS P01 CA109094NIAID NIH HHS R01 AI061807PHS HHS NIAID-46689-5A1PHS HHS NIAID-5RO1AI061807-05
6 · The paper itself

Abstract

TNF receptor superfamily member 25 (TNFRSF25; also known as DR3, and referred to herein as TNFR25) is constitutively and highly expressed by CD4(+)FoxP3(+) Tregs. However, its function on these cells has not been determined. Here we used a TNFR25-specific agonistic monoclonal antibody, 4C12, to study the effects of TNFR25 signaling on Tregs in vivo in mice. Signaling through TNFR25 induced rapid and selective expansion of preexisting Tregs in vivo such that they became 30%-35% of all CD4(+) T cells in the peripheral blood within 4 days. TNFR25-induced Treg proliferation was dependent upon TCR engagement with MHC class II, IL-2 receptor, and Akt signaling, but not upon costimulation by CD80 or CD86; it was unaffected by rapamycin. TNFR25-expanded Tregs remained highly suppressive ex vivo, and Tregs expanded by TNFR25 in vivo were protective against allergic lung inflammation, a mouse model for asthma, by reversing the ratio of effector T cells to Tregs in the lung, suppressing IL-13 and Th2 cytokine production, and blocking eosinophil exudation into bronchoalveolar fluid. Our studies define what we believe to be a novel mechanism for Treg control and important functions for TNFR25 in regulating autoaggression that balance its known role in enhancing autoimmunity.

Indexed as

AnimalsAsthmaDisease Models, AnimalHistocompatibility Antigens Class IIInterleukin-2Lymphocyte ActivationMiceMice, Inbred C57BLOvalbuminPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktReceptors, Tumor Necrosis Factor, Member 25T-Lymphocytes, RegulatoryHistocompatibility Antigens Class IIInterleukin-2OvalbuminPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktReceptors, Tumor Necrosis Factor, Member 25Tnfrsf25 protein, mouse

Identifiers

PMID20890040
PMCPMC2947231
OpenAlexW2162170222

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.