Evidence map›Paper›PMID 12093873›Full record

ArticleThe Journal of experimental medicine2002

T cell costimulation through CD28 depends on induction of the Bcl-xgamma isoform: analysis of Bcl-xgamma-deficient mice.

Qunrui Ye, Barry Press, Stephan Kissler, Xiao-Feng Yang, Linrong Lu, Craig H Bassing, Barry P Sleckman, Marianne Jansson, Vily Panoutsakopoulou, Linda A Trimble and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 36% 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

7 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Article
  3. Higher expression of Bax in regulatory T cells increases vascular inflammation.Frontiers in bioscience : a journal and virtual library · 2008
    Article
  4. Article
  5. Thymic selection can compensate for mutations affecting T cell activation and generate a normal T cell repertoire in mutant mice.Proceedings of the National Academy of Sciences of the United States of America · 2004
    Article
  6. Article
  7. 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

12 authors at 3 institutions in 1 country.

Qunrui YeDepartment of Cancer Immunology and AIDS, Dana-Farber Cancer Institute, Department of Pathology, Harvard Medical School, Boston, MA 02115, USA.
Barry Press
Stephan Kissler
Xiao-Feng Yang
Linrong Lu
Craig H Bassing
Barry P Sleckman
Marianne Jansson
Vily Panoutsakopoulou
Linda A Trimble
Frederick W Alt
Harvey Cantor
Harvard University · USDana-Farber Cancer Institute · USHoward Hughes Medical Institute · US

Funding

Mechanisms that Control IgH Variable Region Exon AssemblyR01AI020047 · NIAID · IMMUNE DISEASE INSTITUTE, INC. · PI ALT, FREDERICK W. · 1985 to 2025
$14.1M
TRANSGENIC MODELS OF T CELL RECEPTOR IMMUNODEFICIENCIESP01AI035714 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI TERHORST, CORNELIS P · 1994 to 2007
$9.3M
Postdoctoral Training Program in AIDS-related ResearchT32AI007386 · NIAID · DANA-FARBER CANCER INSTITUTE · PI CANTOR, HARVEY, ENGELMAN, ALAN N. · 1990 to 2023
$5.3M
THE T-CELL RESPONSE TO ANTIGENR01AI048125 · NIAID · DANA-FARBER CANCER INSTITUTE · PI CANTOR, HARVEY · 2000 to 2021
$5.1M
ASSEMBLY AND EXPRESSION OF IG VARIBLE REGION GENESR37AI020047 · NIAID · IMMUNE DISEASE INSTITUTE, INC. · PI ALT, FREDERICK W · 1991 to 2000
$323k
MHC CLASS I INTERACTIONS REGULATION NAIVE CD8 T CELLF32AI010468 · NIAID · DANA-FARBER CANCER INSTITUTE · PI TRIMBLE, LINDA A · 2000 to 2000
$26k
NIAID NIH HHS AI07386NIAID NIH HHS AI10468NIAID NIH HHS AI20047NIAID NIH HHS AI35714NIAID NIH HHS AI48125NIAID NIH HHS F32 AI010468NIAID NIH HHS P01 AI035714NIAID NIH HHS R01 AI020047NIAID NIH HHS R01 AI048125NIAID NIH HHS R37 AI020047NIAID NIH HHS T32 AI007386PHS HHS A112184PHS HHS A13600
6 · The paper itself

Abstract

The molecular basis of CD28-dependent costimulation of T cells is poorly understood. Bcl-xgamma is a member of the Bcl-x family whose expression is restricted to activated T cells and requires CD28-dependent ligation for full expression. We report that Bcl-xgamma-deficient (Bcl-xgamma-/-) T cells display defective proliferative and cytokine responses to CD28-dependent costimulatory signals, impaired memory responses to proteolipid protein peptide (PLP), and do not develop PLP-induced experimental autoimmune encephalomyelitis (EAE). In contrast, enforced expression of Bcl-xgamma largely replaces the requirement for B7-dependent ligation of CD28. These findings identify the Bcl-xgamma cytosolic protein as an essential downstream link in the CD28-dependent signaling pathway that underlies T cell costimulation.

Indexed as

Adoptive TransferAnimalsApoptosisAutoimmunitybcl-X ProteinCD28 AntigensCD3 ComplexCell CycleCell DivisionCells, CulturedChimeraEncephalomyelitis, Autoimmune, ExperimentalGene Expression RegulationGene TargetingInterleukin-2MiceBcl2l1 protein, mousebcl-X ProteinCD28 AntigensCD3 ComplexInterleukin-2Protein IsoformsProto-Oncogene Proteins c-bcl-2

Identifiers

PMID12093873
PMCPMC2194014
OpenAlexW2095732663

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.