Evidence map›Paper›PMID 32648166›Full record

ReviewCancer immunology, immunotherapy : CII2020

Augmenting engineered T-cell strategies in solid cancers through epigenetic priming.

Aaraby Y Nielsen, Maria Ormhøj, Sofie Traynor, Morten F Gjerstorff

Open access · greenAbstract readReview
In one paragraph

Review in Cancer immunology, immunotherapy : CII, 2020. 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
0.3field-weighted citation impact, top 39% 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, 7 citations in OpenAlex.

  1. Review
  2. Review
  3. IFN-γ- and IL-17-producing CD8Journal for immunotherapy of cancer · 2021
    Article
  4. Review
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

4 authors at 2 institutions in 1 country.

Aaraby Y NielsenDepartment of Cancer and Inflammation Research, Institute of Molecular Medicine, University of Southern Denmark, Odense, Denmark.
Maria OrmhøjDepartment of Health Technology, Technical University of Denmark, Lyngby, Denmark.
Sofie TraynorDepartment of Cancer and Inflammation Research, Institute of Molecular Medicine, University of Southern Denmark, Odense, Denmark.
Morten F GjerstorffDepartment of Cancer and Inflammation Research, Institute of Molecular Medicine, University of Southern Denmark, Odense, Denmark. mgjerstorff@health.sdu.dk.ORCID http://orcid.org/0000-0002-0845-1952
University of Southern Denmark · DKTechnical University of Denmark · DK

Funding

Danish ministry of health 05-0400-41Kræftens Bekæmpelse R1R204-A12255Natur og Univers, Det Frie Forskningsråd 6108-00372ANovo Nordisk Fonden NNF18OC0052303
6 · The paper itself

Abstract

T-cell receptor (TCR)- and chimeric antigen receptor (CAR)-based adoptive cell transfer (ACT) has shown promising results in hematological malignancies, but remains immature in solid cancers. The challenges associated with identification of tumor-specific targets, the heterogenic antigen expression, limited T-cell trafficking to tumor sites and the hostile tumor microenvironment (TME), are all factors contributing to the limited efficacy of ACT therapies against solid tumors. Epigenetic priming of tumor cells and the microenvironment may be a way of overcoming these obstacles and improving the clinical efficacy of adoptive T-cell therapies in the future. Here, we review the current literature and suggest combining epigenetic modulators and ACT strategies as a way of augmenting the efficacy of TCR- and CAR-engineered T cells against solid tumors.

Indexed as

Epigenesis, GeneticNeoplasmsAnimalsAntigens, NeoplasmCombined Modality TherapyDNA Modification MethylasesHistone Deacetylase InhibitorsHumansImmunotherapy, AdoptiveReceptors, Antigen, T-CellT-LymphocytesTumor EscapeTumor MicroenvironmentAntigens, NeoplasmDNA Modification MethylasesHistone Deacetylase InhibitorsReceptors, Antigen, T-CellCancer immunotherapyCancer/testis antigensCombination therapyEpigenetic drugsGenetically modified T cellsSolid tumors

Identifiers

PMID32648166
PMCPMC11027657
OpenAlexW3042163721

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.