Evidence map›Paper›PMID 41028268›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

An Indigenous Workflow for Generating CD19 CAR-T Cells.

Muthuganesh Muthuvel, Sunil Martin

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Article in Methods in molecular biology (Clifton, N.J.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Muthuganesh MuthuvelLaboratory of Synthetic Immunology, Cancer Research Division, Rajiv Gandhi Centre for Biotechnology, Biotechnology Research Innovation Council, Thiruvananthapuram, Kerala, India.
Sunil MartinLaboratory of Synthetic Immunology, Cancer Research Division, Rajiv Gandhi Centre for Biotechnology, Biotechnology Research Innovation Council, Thiruvananthapuram, Kerala, India. sunilmartin03@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

FDA-approved CD19 CAR T cell therapy for treating B-cell lineage malignancies gave impetus to the adoptive immune/cell and gene therapy field. Although tested to a considerable extent, side effects such as immune effector cell-associated neurotoxicity syndrome (ICANS), immune effector cell-associated hematotoxicity (ICAHTs), the high cost of the therapy, and often complicated logistics make the accessibility of this CAR therapy far from the reach of many eligible patients. Therefore, the development of a safe, cost-effective, streamlined indigenous workflow for T-cell expansion, transduction, and CAR T-cell characterization is essential in a preclinical as well as clinical setting. We have optimized a method to develop CD19 CAR T cells from peripheral blood T cells from healthy donors. In this chapter, we describe an indigenous protocol for the generation and characterization of CD19 CAR T cells via lentiviral transduction to understand the immunology or possible downstream applications.

Indexed as

Antigens, CD19Immunotherapy, AdoptiveReceptors, Chimeric AntigenT-LymphocytesHumansLentivirusReceptors, Antigen, T-CellTransduction, GeneticWorkflowAntigens, CD19CD19 molecule, humanReceptors, Antigen, T-CellReceptors, Chimeric AntigenAntitumor functionsCD19 CAR T cellsFlow cytometryLentiviral production

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Registered trials

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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.