免疫原性
单克隆抗体
癌症
药物开发
医学
癌症研究
计算生物学
癌细胞
抗体
药品
药理学
生物
免疫学
内科学
作者
James R. Kintzing,Maria V. Filsinger Interrante,Jennifer R. Cochran
标识
DOI:10.1016/j.tips.2016.10.005
摘要
Protein-based therapeutics have been revolutionizing the oncology space since they first appeared in the clinic two decades ago. Unlike traditional small-molecule chemotherapeutics, protein biologics promote active targeting of cancer cells by binding to cell-surface receptors and other markers specifically associated with or overexpressed on tumors versus healthy tissue. While the first approved cancer biologics were monoclonal antibodies, the burgeoning field of protein engineering is spawning research on an expanded range of protein formats and modifications that allow tuning of properties such as target-binding affinity, serum half-life, stability, and immunogenicity. In this review we highlight some of these strategies and provide examples of modified and engineered proteins under development as preclinical and clinical-stage drug candidates for the treatment of cancer.
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