Natural and revolutionary tumor-specific T-cell therapy.

Nat Prod Bioprospect

Yunnan Characteristic Plant Extraction Laboratory, Key Laboratory of Medicinal Chemistry for Natural Resource, Ministry of Education, Yunnan Key Laboratory of Research and Development for Natural Products, School of Pharmacy, School of Chemical Science and Technology, Yunnan University, Kunming, 650500, People's Republic of China.

Published: August 2024

AI Article Synopsis

  • * In a new approach, researchers developed a tumor-specific T-cell therapy by co-culturing MHC cancer cells with naïve T-cells, which produced effective T-cells that specifically target tumors without needing lentivirus or professional antigen-presenting cells.
  • * This innovative therapy demonstrated significant success in mouse models, reducing tumor nodules by 90% and improving overall survival from 30 to 76 days, while minimizing risks related to secondary cancers and non-specific attacks on healthy cells.

Article Abstract

Recently the FDA conducted a risk investigation and labeled the Boxed Warning for all BCMA- and CD19-directed CAR-T cell therapy, so does it mean that the public must take risk of secondary cancer to receive cell therapy? Here, without lentivirus and professional antigen presenting cell application, a novel tumor-specific T-cell therapy was successfully developed only by co-culturing MHC cancer cells and Naïve-T cells under the CD28 co-stimulatory signals. These tumor-specific T-cells could be separated through cell size and abundantly produced from peripheral blood, and would spontaneously attack target cells that carrying the same tumor antigen while avoiding others in vitro test. Moreover, it markedly decreased 90% tumor nodules companying with greatly improving overall survival (76 days vs 30 days) after twice infusion back to mice. This work maximally avoided the risks of secondary cancer and non-specific killing, and might open a revolutionary beginning of natural tumor-specific T-cell therapy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11333775PMC
http://dx.doi.org/10.1007/s13659-024-00472-wDOI Listing

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