Evidence map›Paper›PMID 22642331›Full record

ArticleImmunotherapy2012

Depletion of Tregs for adoptive T-cell therapy using CD44 and CD137 as selection markers.

Brian G Till, Oliver W Press

Open access · greenAbstract read
In one paragraph

Article in Immunotherapy, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.2field-weighted citation impact, top 44% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. CD137-expressing regulatory T cells in cancer and autoimmune diseases.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review
  2. Tissue Resident Foxp3Frontiers in immunology · 2022
    Review
  3. Review
  4. 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

2 authors at 1 institution in 1 country.

Brian G TillClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Oliver W Press
Fred Hutch Cancer Center · US

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Marian Esvelt · 1985 to 2026
$296.4M
Anti-CD20 CTL for Therapy of Mantle Cell LymphomaR21CA117131 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PRESS, OLIVER W. · 2006 to 2007
$581k
NCI NIH HHS CA117131NCI NIH HHS P30 CA015704NCI NIH HHS R21 CA117131
6 · The paper itself

Abstract

Several types of cancer have been shown to be susceptible to cellular immune responses, leading to investigations using various forms of T cell-based, tumor-directed immunotherapy. One potential obstacle for the successful application of these therapies is the suppressive function of Tregs. Goldstein and colleagues evaluate a strategy to identify and remove Tregs from an adoptive T-cell therapy product generated by in vivo vaccination. They demonstrate that the depletion of Tregs characterized by CD44 and CD137 expression enhances antitumor immunity in their mouse model.

Indexed as

Immunotherapy, AdoptiveLymphocyte DepletionAnimalsBiomarkersCell SeparationFlow CytometryHumansHyaluronan ReceptorsLymphoma, B-CellMiceMice, Inbred C57BLRadiation ChimeraT-LymphocytesT-Lymphocytes, RegulatoryT-Lymphocyte SubsetsTumor Necrosis Factor Receptor Superfamily, Member 9BiomarkersHyaluronan ReceptorsTumor Necrosis Factor Receptor Superfamily, Member 9

Identifiers

PMID22642331
PMCPMC3390965
OpenAlexW2098829579

What OpenQuestion holds

Textmetadata
LicenceTDM
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.