Evidence map›Paper›PMID 19023118›Full record

ArticleBlood2009

Impaired negative regulation of homeostatically proliferating T cells.

Anna Shvets, Rabindranath Chakrabarti, Rosana Gonzalez-Quintial, Roberto Baccala, Argyrios N Theofilopoulos, Gérald J Prud'homme

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Blood, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02771197 (Phase II Trial of Lymphodepletion and Anti-PD-1 Blockade to Reduce Relapse in High Risk AML Patients Who Are Not Eligible for Allogeneic Stem Cell Transplantation), which is not on this map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.7field-weighted citation impact, top 32% 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.

NCT02771197 phase2completednot on this mapstarted 2016, after this paper: background citation

Phase II Trial of Lymphodepletion and Anti-PD-1 Blockade to Reduce Relapse in High Risk AML Patients Who Are Not Eligible for Allogeneic Stem Cell Transplantation

TypeinterventionalSponsorNorthside Hospital, Inc.Ran2016 to 2023Enrolled20ConditionsAcute Myeloid LeukemiaArmsFludarabine, Melphalan, Pembrolizumab
3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Article
  6. CD18 is required for optimal lymphopenia-induced proliferation of mouse T cells.American journal of physiology. Gastrointestinal and liver physiology · 2012
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. 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

6 authors at 4 institutions in 3 countries.

Anna ShvetsDepartment of Laboratory Medicine, St Michael's Hospital and University of Toronto, Toronto, ON.
Rabindranath Chakrabarti
Rosana Gonzalez-Quintial
Roberto Baccala
Argyrios N Theofilopoulos
Gérald J Prud'homme
Scripps Research Institute · USSt Michaels Hospital · GBSt. Michael's Hospital · CAUniversity of Toronto · CA

Funding

T Cell Homeostasis in Systemic AutoimmunityR01AR031203 · NIAMS · SCRIPPS RESEARCH INSTITUTE, THE · PI THEOFILOPOULOS, ARGYRIOS N · 1986 to 2012
$4.9M
NCI NIH HHS CA10902NIAMS NIH HHS AR31203NIAMS NIH HHS R01 AR031203
6 · The paper itself

Abstract

Acute lymphopenia-induced homeostatic proliferation (HP) of T cells promotes antitumor immunity, but the mechanism is unclear. We hypothesized that this is due to a lack of inhibitory signals that allows activation of T cells with low affinity for self-antigens. Tumors resist immunity in part by expressing inhibitory molecules such as PD-1 ligand 1 (PD-L1), B7-H4, and TGF-beta. In irradiated mice undergoing HP, we found that T cells displayed a severe deficit in the activation-induced expression of inhibitory molecules PD-1 and CTLA-4, and TGF-beta1-induced expression of Foxp3. HP T cells were also less suppressed by B7-H4/Ig and, unlike control T cells, failed to produce IL-10 in response to this molecule. This deficiency in regulation was reversed as normal T-cell numbers were restored. We conclude that T cells are weakly regulated by inhibitory molecules during the acute phase of HP, which could explain their increased effectiveness in cancer immunotherapy.

Indexed as

AnimalsAntigens, CDAntigens, DifferentiationAutoantigensB7-1 AntigenCell ProliferationCTLA-4 AntigenForkhead Transcription FactorsHomeostasisLymphopeniaMiceProgrammed Cell Death 1 ReceptorT-LymphocytesTransforming Growth Factor betaV-Set Domain-Containing T-Cell Activation Inhibitor 1Antigens, CDAntigens, DifferentiationAutoantigensB7-1 AntigenCTLA-4 AntigenCtla4 protein, mouseForkhead Transcription FactorsFoxp3 protein, mousePdcd1 protein, mouseProgrammed Cell Death 1 ReceptorTransforming Growth Factor betaV-Set Domain-Containing T-Cell Activation Inhibitor 1Vtcn1 protein, mouse

Identifiers

PMID19023118
PMCPMC2948436
OpenAlexW1963764926

What OpenQuestion holds

Textmetadata
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.