Jul 2026· Sheng wu gong cheng xue bao = Chinese journal of biotechnology· Vol 42 7, pp.
3138-3153
· 0 citations
Medicine
TL;DR
Results indicate that the 24 h rapid production strategy is feasible and provides a promising technical approach to shorten patient waiting time, reduce production costs, and generate functionally improved CAR-T cell products for clinical translation.
The main delivery platforms under clinical investigation are described, focusing on lentiviral vectors and lipid nanoparticles, and their differences in terms of mechanisms of action, associated risks, and optimization strategies are discussed.
François Vilcot, Carole-Anne Brugère, Jaime Fuentealba et al.· Bulletin du Cancer· 0 citations
In vivo CAR-T is poised to broaden the reach of cellular immunotherapy, provided that its development is guided by rigorous pharmacology, chemistry, manufacturing and controls, and long-term molecular safety surveillance.
Wan-Ting Wang, Yujia Cai, Xuanming Yang et al.· Immunity & Inflammation· 0 citations
Although still in its infancy, in vivo genetic engineering shows promise for CAR T cell therapy in a wide range of cancer patients and has the potential to reprogram patients’ immunity in autoimmunity, chronic infections, and regenerative medicine.
Markus Barden, D. Harrer, Hinrich Abken· Expert Opinion on Biological...· 0 citations
Chimeric antigen receptor (CAR) T-cell therapy has transformed the treatment of several hematological malignancies, but its broader application remains constrained by the complexity, cost, and time required for conventional ex vivo manufacturing. In vivo CAR T-cell therapy has emerged as a promising next-generation str...
Chimeric antigen receptor T‐cell (CAR‐T) therapy is a transformative tumor immunotherapy that redirects autologous T cells to eliminate malignant cells. However, its broader clinical translation is constrained by complex and costly ex vivo manufacturing, variable product quality, and limited control over in vivo activi...
Zhen-Xin Bai, Ming Yi, Sheng-Tao Hu et al.· MedComm· 0 citations
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