Evidence map›Paper›PMID 32899932›Full record

ReviewInternational journal of molecular sciences2020

In Vitro-Transcribed mRNA Chimeric Antigen Receptor T Cell (IVT mRNA CAR T) Therapy in Hematologic and Solid Tumor Management: A Preclinical Update.

Thangavelu Soundara Rajan, Agnese Gugliandolo, Placido Bramanti, Emanuela Mazzon

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
2.8field-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

45 citing papers in PubMed, 67 citations in OpenAlex.

  1. Article
  2. Review
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  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Engineering mRNA CAR-T Cells for Cancer Immunotherapy.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  12. Article
  13. Review
  14. Article
  15. Article
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  17. mRNA-Engineered CD5-CAR-γδTAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  18. Review
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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

4 authors at 2 institutions in 2 countries.

Thangavelu Soundara RajanDepartment of Biotechnology, School of Life Sciences, Karpagam Academy of Higher Education, Coimbatore 641021, India.ORCID 0000-0001-8728-6176
Agnese GugliandoloIRCCS Centro Neurolesi "Bonino-Pulejo", Via Palermo, Contrada Casazza-S.S.113, 98124 Messina, Italy.
Placido BramantiIRCCS Centro Neurolesi "Bonino-Pulejo", Via Palermo, Contrada Casazza-S.S.113, 98124 Messina, Italy.
Emanuela MazzonIRCCS Centro Neurolesi "Bonino-Pulejo", Via Palermo, Contrada Casazza-S.S.113, 98124 Messina, Italy.
Centro Neurolesi Bonino Pulejo · ITKarpagam Academy of Higher Education · IN

Funding

Ministero della Salute -
6 · The paper itself

Abstract

Adoptive T cell immunotherapy has received considerable interest in the treatment of cancer. In recent years, chimeric antigen receptor T cell (CAR T) therapy has emerged as a promising therapy in cancer treatment. In CAR T therapy, T cells from the patients are collected, reprogrammed genetically against tumor antigens, and reintroduced into the patients to trigger an immense immune response against cancer cells. CAR T therapy is successful in hematologic malignancies; however, in solid tumors, CAR T therapy faces multiple challenges, including the on-target off-tumor phenomenon, as most of the tumor-associated antigens are expressed in normal cells as well. Consequently, a transient in vitro-transcribed anti-mRNA-based CAR T cell (IVT mRNA CAR T) approach has been investigated to produce controlled cytotoxicity for a limited duration to avoid any undesirable effects in patients. In vitro and in vivo studies demonstrated the therapeutic ability of mRNA-engineered T cells in solid tumors, including melanoma, neuroblastoma and ovarian cancer; however, very few clinical trials are registered. In the present review, we discuss the effect of IVT mRNA CAR T therapy in preclinical studies related to hematologic malignancies and solid tumor management. In addition, we discuss the clinical trial studies based on IVT mRNA CAR T therapy in cancer.

Indexed as

AnimalsCells, CulturedDisease Models, AnimalFemaleGenetic TherapyHematologic NeoplasmsHumansImmunotherapy, AdoptiveIn Vitro TechniquesMaleNeoplasmsReceptors, Antigen, T-CellReceptors, Chimeric AntigenRNA, MessengerTranscription, GeneticReceptors, Antigen, T-CellReceptors, Chimeric AntigenRNA, Messengeradoptive T cell immunotherapychimeric antigen receptorhematologic tumorsin vitro-transcribed mRNAsolid tumorsT cells

Identifiers

PMID32899932
PMCPMC7556036
OpenAlexW3083625272

What OpenQuestion holds

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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.