Evidence map›Paper›PMID 22400040›Full record

ReviewClinical & developmental immunology2012

Cytotoxic chemotherapy and CD4+ effector T cells: an emerging alliance for durable antitumor effects.

Zhi-Chun Ding, Gang Zhou

Open access · goldAbstract readReview
In one paragraph

Review in Clinical & developmental immunology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

37 citing papers in PubMed, 57 citations in OpenAlex.

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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.

Zhi-Chun DingCancer Immunotherapy Program, Cancer Center, Georgia Health Sciences University, Augusta, GA 30912, USA.
Gang Zhou
Augusta University Health · US

Funding

Reversing tumor-specific CD4+ T-cell tolerance to control relapse after chemotherR01CA158202 · NCI · AUGUSTA UNIVERSITY · PI ZHOU, GANG · 2012 to 2016
$1.4M
NCI NIH HHS R01 CA158202
6 · The paper itself

Abstract

Standard cytotoxic chemotherapy can initially achieve high response rates, but relapses often occur in patients and represent a severe clinical problem. As increasing numbers of chemotherapeutic agents are found to have immunostimulatory effects, there is a growing interest to combine chemotherapy and immunotherapy for synergistic antitumor effects and improved clinical benefits. Findings from recent studies suggest that highly activated, polyfunctional CD4+ effector T cells have tremendous potential in strengthening and sustaining the overall host antitumor immunity in the postchemotherapy window. This review focuses on the latest progresses regarding the impact of chemotherapy on CD4+ T-cell phenotype and function and discusses the prospect of exploiting CD4+ T cells to control tumor progression and prevent relapse after chemotherapy.

Indexed as

Secondary PreventionAntineoplastic AgentsCD4-Positive T-LymphocytesCombined Modality TherapyHumansImmunomodulationImmunotherapyLymphocyte ActivationNeoplasmsAntineoplastic Agents

Identifiers

PMID22400040
PMCPMC3286900
OpenAlexW2026164481

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.