免疫原性
嵌合抗原受体
医学
T细胞受体
转化研究
生物仿制药
药物开发
T细胞
免疫学
药理学
内科学
抗原
免疫系统
药品
病理
作者
Jochem Gokemeijer,Nanda Balasubramanian,K. OGASAWARA,Joanna Grudzinska‐Goebel,Vijay Upreti,Hardik Mody,Siddha Kasar,Venkata R. Vepachedu,Weifeng Xu,Swati Gupta,Edit Tarcsa,Robert Dodge,Kate Herr,Tong‐Yuan Yang,Sophie Tourdot,Vibha Jawa
摘要
CAR-T therapies have shown remarkable efficacy against hematological malignancies in the clinic over the last decade and new studies indicate that progress is being made to use these novel therapies to target solid tumors as well as treat autoimmune disease. Innovation in the field, including TCR-T, allogeneic or "off the shelf" CAR-T, and autoantigen/armored CAR-Ts are likely to increase the efficacy and applications of these therapies. The unique aspects of these cell-based therapeutics; patient-derived cells, intracellular expression, in vivo expansion, and phenotypic changes provide unique bioanalytical challenges to develop pharmacokinetic and immunogenicity assessments. The International Consortium for Innovation and Quality in Pharmaceutical Development (IQ) Translational and ADME Sciences Leadership Group (TALG) has brought together a group of industry experts to discuss and consider these challenges. In this white paper, we present the IQ consortium perspective on the best practices and considerations for bioanalytical and immunogenicity aspects toward the optimal development of CAR-T and TCR-T cell therapies.
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