双特异性抗体
抗体
效应器
表位
计算生物学
抗原
嵌合抗原受体
受体
免疫系统
免疫学
化学
计算机科学
生物
免疫疗法
单克隆抗体
生物化学
作者
David L. Niquille,Kyle M. Fitzgerald,Nimish Gera
出处
期刊:mAbs
[Informa]
日期:2024-03-04
卷期号:16 (1)
被引量:7
标识
DOI:10.1080/19420862.2024.2310890
摘要
Biparatopic antibodies (bpAbs) bind distinct, non-overlapping epitopes on an antigen. This unique binding mode enables new mechanisms of action beyond monospecific and bispecific antibodies (bsAbs) that can make bpAbs effective therapeutics for various indications, including oncology and infectious diseases. Biparatopic binding can lead to superior affinity and specificity, promote antagonism, lock target conformation, and result in higher-order target clustering. Such antibody-target complexes can elicit strong agonism, increase immune effector function, or result in rapid target downregulation and lysosomal trafficking. These are not only attractive properties for therapeutic antibodies but are increasingly being explored for other modalities such as antibody-drug conjugates, T-cell engagers and chimeric antigen receptors. Recent advances in bpAb engineering have enabled the construction of ever more sophisticated formats that are starting to show promise in the clinic.
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