Evidence map›Paper›PMID 40877510›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2025

mRNA-Based Engineering of Viral Antigen-Specific TCR-T Cells.

He Shan, Antonio Bertoletti, Anthony Tanoto Tan

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

He ShanSignature Research Program in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore.
Antonio BertolettiSignature Research Program in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore. antonio@duke-nus.edu.sg.
Anthony Tanoto TanSignature Research Program in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To redirect T cells toward target cells, they can be engineered ex vivo to express antigen-specific T cell receptors (TCRs), creating TCR-engineered T cells (TCR-T). In this chapter, we provide a streamlined protocol for generating autologous mRNA-electroporated, viral antigen-specific, immunosuppressive drug-resistant armored (IDRA) TCR-T cell therapy products in a laboratory setting. We also discuss the advantages of transient mRNA electroporation over permanent genetic modification technologies for our specific application. Finally, we present a protocol to evaluate the in vitro and in vivo functionality of our TCR-T cell therapy product.

Indexed as

Antigens, ViralGenetic EngineeringReceptors, Antigen, T-CellReceptors, Chimeric AntigenRNA, MessengerT-LymphocytesElectroporationHumansImmunotherapy, AdoptiveAntigens, ViralReceptors, Antigen, T-CellReceptors, Chimeric AntigenRNA, MessengerAdoptive T cell transferIDRAmRNA electroporationT cell in vitro expansionTCR-T cell therapyVirus-specific T cells

Identifiers

PMID40877510

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.