Evidence map›Paper›PMID 37387794›Full record

ArticleMolecular therapy oncolytics2023

Enhancing the effectiveness of γδ T cells by mRNA transfection of chimeric antigen receptors or bispecific T cell engagers.

Scott A Becker, Brian G Petrich, Bing Yu, Kristopher A Knight, Harrison C Brown, Sunil S Raikar, Christopher B Doering, H Trent Spencer

Abstract read
In one paragraph

Article in Molecular therapy oncolytics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. A GD (Gamma-Delta) type of cancel culture.Immuno-oncology technology · 2024
    Review
  9. Article
  10. Review
  11. Directing the migration of serum-free,Frontiers in immunology · 2024
    Article
  12. Article
  13. Mechanisms and Applications of γδ T Cells in Anti-Tumor Immunity.Cancer control : journal of the Moffitt Cancer Center
    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

8 authors.

Scott A BeckerMolecular and System Pharmacology Program, Graduate Division of Biological and Biomedical Sciences, Emory University, Atlanta, GA, USA.
Brian G PetrichExpression Therapeutics, Inc, Tucker, GA, USA.
Bing YuExpression Therapeutics, Inc, Tucker, GA, USA.
Kristopher A KnightMolecular and System Pharmacology Program, Graduate Division of Biological and Biomedical Sciences, Emory University, Atlanta, GA, USA.
Harrison C BrownExpression Therapeutics, Inc, Tucker, GA, USA.
Sunil S RaikarAflac Cancer and Blood Disorders Center, Department of Pediatrics, Emory University School of Medicine and Children's Healthcare of Atlanta, Atlanta, GA, USA.
Christopher B DoeringMolecular and System Pharmacology Program, Graduate Division of Biological and Biomedical Sciences, Emory University, Atlanta, GA, USA.
H Trent SpencerMolecular and System Pharmacology Program, Graduate Division of Biological and Biomedical Sciences, Emory University, Atlanta, GA, USA.

Funding

Gamma delta T-cell immunotherapy for T-cell acute lymphoblastic leukemiaK08CA248962 · NCI · EMORY UNIVERSITY · PI RAIKAR, SUNIL SUDHIR · 2020 to 2024
$1.1M
NCI NIH HHS K08 CA248962
6 · The paper itself

Abstract

Adoptive cell therapy (ACT) utilizing γδ T cells is becoming a promising option for the treatment of cancer, because it offers an off-the-shelf allogeneic product that is safe, potent, and clinically effective. Approaches to engineer or enhance immune-competent cells for ACT, like expression of chimeric antigen receptors (CARs) or combination treatments with bispecific T cell engagers, have improved the specificity and cytotoxic potential of ACTs and have shown great promise in preclinical and clinical settings. Here, we test whether electroporation of γδ T cells with CAR or secreted bispecific T cell engager (sBite) mRNA is an effective approach to improve the cytotoxicity of γδ T cells. Using a CD19-specific CAR, approximately 60% of γδ T cells are modified after mRNA electroporation and these cells show potent anticancer activity

Indexed as

bispecific T cell engagercancer immunotherapyCAR T cellselectroporationgamma delta T cells

Identifiers

PMID37387794
PMCPMC10300408

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.