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Synthetic biology approaches for enhancing safety and specificity of CAR-T cell therapies for solid cancers.
Russell, Grace C; Hamzaoui, Yassin; Rho, Daniel; Sutrave, Gaurav; Choi, Joseph S; Missan, Dara S; Reckard, Gabrielle A; Gustafson, Michael P; Kim, Gloria B.
Afiliación
  • Russell GC; Department of Physiology and Biomedical Engineering, Mayo Clinic Arizona, Scottsdale, Arizona, USA.
  • Hamzaoui Y; Department of Physiology and Biomedical Engineering, Mayo Clinic Arizona, Scottsdale, Arizona, USA.
  • Rho D; Department of Physiology and Biomedical Engineering, Mayo Clinic Arizona, Scottsdale, Arizona, USA.
  • Sutrave G; The University of Sydney, Sydney, Australia; Department of Haematology, Westmead Hospital, Sydney, Australia; Immuno & Gene Therapy Committee, International Society for Cell and Gene Therapy, Vancouver, Canada.
  • Choi JS; Department of Physiology and Biomedical Engineering, Mayo Clinic Arizona, Scottsdale, Arizona, USA.
  • Missan DS; Department of Laboratory Medicine and Pathology, Mayo Clinic Arizona, Phoenix, Arizona, USA.
  • Reckard GA; Department of Laboratory Medicine and Pathology, Mayo Clinic Arizona, Phoenix, Arizona, USA.
  • Gustafson MP; Immuno & Gene Therapy Committee, International Society for Cell and Gene Therapy, Vancouver, Canada; Department of Laboratory Medicine and Pathology, Mayo Clinic Arizona, Phoenix, Arizona, USA; Department of Immunology, Mayo Clinic Arizona, Scottsdale, Arizona, USA.
  • Kim GB; Department of Physiology and Biomedical Engineering, Mayo Clinic Arizona, Scottsdale, Arizona, USA; Department of Immunology, Mayo Clinic Arizona, Scottsdale, Arizona, USA. Electronic address: kim.gloria2@mayo.edu.
Cytotherapy ; 26(8): 842-857, 2024 Aug.
Article en En | MEDLINE | ID: mdl-38639669
ABSTRACT
CAR-T cell therapies have been successful in treating numerous hematologic malignancies as the T cell can be engineered to target a specific antigen associated with the disease. However, translating CAR-T cell therapies for solid cancers is proving more challenging due to the lack of truly tumor-associated antigens and the high risk of off-target toxicities. To combat this, numerous synthetic biology mechanisms are being incorporated to create safer and more specific CAR-T cells that can be spatiotemporally controlled with increased precision. Here, we seek to summarize and analyze the advancements for CAR-T cell therapies with respect to clinical implementation, from the perspective of synthetic biology and immunology. This review should serve as a resource for further investigation and growth within the field of personalized cellular therapies.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Linfocitos T / Inmunoterapia Adoptiva / Biología Sintética / Receptores Quiméricos de Antígenos / Neoplasias Idioma: En Revista: Cytotherapy Asunto de la revista: TERAPEUTICA Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Linfocitos T / Inmunoterapia Adoptiva / Biología Sintética / Receptores Quiméricos de Antígenos / Neoplasias Idioma: En Revista: Cytotherapy Asunto de la revista: TERAPEUTICA Año: 2024 Tipo del documento: Article