Car-T Cell Therapy: A Paradigm Shift in Cancer Treatment
Chimeric antigen receptor T-cell (CAR-T) therapy, a major application of precision and customized medicine, has emerged as a revolutionary advancement in cancer immunotherapy. CAR-T therapy genetically alters a patient's T cells to express synthetic receptors that accurately identify tumor-associated antigens in an MHC-independent manner, resulting in potent and targeted anticancer activity. This study provides an overview of the fundamental ideas of CAR-T cell therapy, including T-cell biology, CAR structure and generations, and the production process, which includes leukapheresis, genetic engineering, ex vivo expansion, conditioning chemotherapy, and patient injection. The mechanisms underlying CAR-T-mediated tumor destruction include antigen recognition, T-cell activation, cytotoxic effector pathways, cytokine production, and tumor lysis. We examine the most recent FDA-approved CAR-T treatments and their clinical applications. We also discuss novel applications in solid tumors and associated issues, such as immune-suppressive tumor microenvironment and antigen heterogeneity. The primary adverse effects, such as immune effector cell-associated neurotoxicity syndrome and cytokine release syndrome, are also discussed in the review along with current treatments. Finally, the drawbacks of CAR-T therapy, recent advances in technology, and the evolving CAR-T environment in India including domestic innovations are examined. Keywords: Tumor; Cancer immunotherapy; Precision medicine; Cytokine release syndrom
Authors
- R. S. Lokhande (ORCID: https://orcid.org/0000-0002-6006-4757)
- Pratiksha K. Hajare (ORCID: https://orcid.org/0000-0002-0995-2070)
- Shatakshi Prakash Patki
- Nikita Sarjerao Game
Institutions
- Savitribai Phule Pune University (IN)
Publication Details
- Journal
- Journal of Drug Delivery and Therapeutics
- Published
- 2026-03-15
- DOI
- https://doi.org/10.22270/jddt.v16i3.7599
- Primary Topic
- CAR-T cell therapy research
- Type
- article
- Field-Weighted Citation Impact
- 0.00