Natural and revolutionary tumor-specific T-cell therapy

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<sup>+</sup> 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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Publication Details

Journal
Natural Products and Bioprospecting
Published
2024-08-19
DOI
https://doi.org/10.1007/s13659-024-00472-w
Primary Topic
CAR-T cell therapy research
Type
article
Field-Weighted Citation Impact
0.00

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article

Natural and revolutionary tumor-specific T-cell therapy

Yun‐Li Zhao, Xiao‐Dong Luo, Li‐Xing Zhao, Zhi Dai et al.
Natural Products and Bioprospecting
CAR-T cell therapy research
article

Natural and revolutionary tumor-specific T-cell therapy

Yun‐Li Zhao, Xiao‐Dong Luo, Li‐Xing Zhao, Zhi Dai, Xue-Meng Liu
article en

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<sup>+</sup> 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.

Natural Products and BioprospectingVol. 14(1)
Yunnan University (CN)
Yunnan University
Good health and well-being
Openalex Percentile: Top 77%
CAR-T cell therapy research
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