单克隆抗体
药品
背景(考古学)
抗体-药物偶联物
医学
概念证明
计算生物学
计算机科学
药理学
抗体
免疫学
生物
操作系统
古生物学
作者
Charalampos Theocharopoulos,Panagiotis-Petros Lialios,Michael Samarkos,Helen Gogas,Dimitrios C. Ziogas
出处
期刊:Vaccines
[MDPI AG]
日期:2021-09-29
卷期号:9 (10): 1111-1111
被引量:19
标识
DOI:10.3390/vaccines9101111
摘要
In the era of precision medicine, antibody-based therapeutics are rapidly enriched with emerging advances and new proof-of-concept formats. In this context, antibody-drug conjugates (ADCs) have evolved to merge the high selectivity and specificity of monoclonal antibodies (mAbs) with the cytotoxic potency of attached payloads. So far, ten ADCs have been approved by FDA for oncological indications and many others are currently being tested in clinical and preclinical level. This paper summarizes the essential components of ADCs, from their functional principles and structure up to their limitations and resistance mechanisms, focusing on all latest bioengineering breakthroughs such as bispecific mAbs, dual-drug platforms as well as novel linkers and conjugation chemistries. In continuation of our recent review on anticancer implication of ADC's technology, further insights regarding their potential usage outside of the oncological spectrum are also presented. Better understanding of immunoconjugates could maximize their efficacy and optimize their safety, extending their use in everyday clinical practice.
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