Evidence map›Paper›PMID 12695569›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2003

Effector CD8 T cells possess suppressor function after 4-1BB and Toll-like receptor triggering.

Lara Myers, Chikara Takahashi, Robert S Mittler, Robert J Rossi, Anthony T Vella

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

28 citing papers in PubMed, 64 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Immunology of Adenoviral Vectors in Cancer Therapy.Molecular therapy. Methods & clinical development · 2019
    Review
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. The oxazolidinone derivative locostatin induces cytokine appeasement.Journal of immunology (Baltimore, Md. : 1950) · 2009
    Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. Article
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

5 authors at 3 institutions in 1 country.

Lara MyersDivision of Immunology, University of Connecticut Health Center, Farmington, CT 06032, USA.
Chikara Takahashi
Robert S Mittler
Robert J Rossi
Anthony T Vella
Emory University · USOregon State University · USUConn Health · US

Funding

PROINFLAMMATORY CYTOKINES BLOCK T CELL DEATH IN VIVOR01AI042858 · NIAID · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI VELLA, ANTHONY T · 1999 to 2016
$4.9M
BASIC IMMUNOLOGY &IMMUNOLOGIC CELL INJURYT32AI007080 · NIAID · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI ADLER, ADAM J, VELLA, ANTHONY T · 1985 to 2012
$1.4M
Understanding the mechanism of 4-1BB costimulationR21AI052108 · NIAID · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI VELLA, ANTHONY T. · 2002 to 2002
$326k
NIAID NIH HHS AI42858ANIAID NIH HHS R21 AI052108NIAID NIH HHS R21AI52108-01NIAID NIH HHS T32 AI007080NIAID NIH HHS T32-AI07080
6 · The paper itself

Abstract

To better understand how innate and adaptive immune responses interact with each other, we combined 4-1BB T cell costimulation with specific adjuvants to determine whether these treatments would influence specific T cell expansion and function in vivo. In the presence of 4-1BB ligation and Toll-like receptor 3 (TLR)3 and/or TLR4 triggering, CD8 T cell clonal expansion and survival was augmented profoundly. Specific T cells primed in vivo with TLR ligands responded normally to in vitro recall stimulus, but, surprisingly, copriming with 4-1BB costimulation significantly impaired the recall response even though many more specific effector T cells were rescued in vivo. Here, we demonstrate that the rescued CD8 T cells suppressed CD4 T cell proliferation via a type beta transforming growth factor-dependent mechanism. Thus, 4-1BB and TLR ligands induce survival of specific effector CD8 T cells with suppressive recall potential, which may explain the dual role that 4-1BB activation plays in mediating tumor clearance and prevention of autoimmune disease.

Indexed as

Drosophila ProteinsAnimalsAntigens, CDCD8-Positive T-LymphocytesFlow CytometryMembrane GlycoproteinsMiceReceptors, Cell SurfaceReceptors, Nerve Growth FactorReceptors, Tumor Necrosis FactorToll-Like Receptor 3Toll-Like Receptor 4Toll-Like ReceptorsTumor Necrosis Factor Receptor Superfamily, Member 9Antigens, CDDrosophila ProteinsMembrane GlycoproteinsReceptors, Cell SurfaceReceptors, Nerve Growth FactorReceptors, Tumor Necrosis FactorTnfrsf9 protein, mouseToll-Like Receptor 3Toll-Like Receptor 4Toll-Like ReceptorsTumor Necrosis Factor Receptor Superfamily, Member 9

Identifiers

PMID12695569
PMCPMC154348
OpenAlexW2046767368

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.