4.6 Article Proceedings Paper

Current Status: Site-Specific Antibody Drug Conjugates

期刊

JOURNAL OF CLINICAL IMMUNOLOGY
卷 36, 期 -, 页码 S100-S107

出版社

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s10875-016-0265-6

关键词

Antibody drug conjugates(ADCs); drug-antibody ratio (DAR); site-specific conjugation; therapeutic window; unnatural amino acids (UAA); monomethyl auristatin E/F (MMAE/MMAF); THIOMAB; microbial transglutaminase (MTG); formylglycine generating enzyme(FGE); Sortase A; tubulin tyrosine ligase (TTL); Tub-tag

资金

  1. Deutsche Forschungsgemeinschaft [SPP1623, HA 4468/9-1, LE 721/13-1]
  2. Fonds der Chemischen Industrie (FCI)

向作者/读者索取更多资源

Antibody drug conjugates (ADCs), a promising class of cancer biopharmaceuticals, combine the specificity of therapeutic antibodies with the pharmacological potency of chemical, cytotoxic drugs. Ever since the first ADCs on the market, a plethora of novel ADC technologies has emerged, covering as diverse aspects as antibody engineering, chemical linker optimization and novel conjugation strategies, together aiming at constantly widening the therapeutic window for ADCs. This review primarily focuses on novel chemical and biotechnological strategies for the site-directed attachment of drugs that are currently validated for 2nd generation ADCs to promote conjugate homogeneity and overall stability.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据