Implications of receptor-mediated endocytosis and intracellular trafficking dynamics in the development of antibody drug conjugates

被引:242
作者
Ritchie, Michael [1 ]
Tchistiakova, Lioudmila [1 ]
Scott, Nathan [1 ]
机构
[1] Pfizer Global Res & Dev, Global Biotherapeut Technol, Cambridge, MA USA
关键词
endocytosis; endosomal sorting; antibody engineering; ADC; lysosome; HER2; affinity; linker payload; SINGLE-CHAIN FV; ACUTE MYELOID-LEUKEMIA; GEMTUZUMAB OZOGAMICIN; MONOCLONAL-ANTIBODY; HUMAN PROLACTIN; BREAST-CANCER; TRASTUZUMAB EMTANSINE; MOLECULAR-MECHANISMS; ENDOSOME MATURATION; TUMOR PENETRATION;
D O I
10.4161/mabs.22854
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The use of antibody-drug conjugates (ADCs) as a therapeutic platform to treat cancer has recently gained substantial momentum. This therapeutic modality has the potential to increase the efficacy and reduce the systemic toxicity associated with current therapeutic regimens. The efficacy of ADCs, however, relies on the proper exploitation of intracellular sorting dynamics of the antigen as well as the specificity, selectivity and pharmacokinetic properties of the antibody itself. Our understanding of endocytosis and endosomal trafficking of receptors has appreciably increased in recent years, as improvements in the assays used to study these events have resolved many of the molecular mechanisms regulating these processes. As a result, we now have the knowledge necessary to exploit these pathways efficiently to improve the efficacy of antibody-based therapy. This review discusses some recent studies that have explored how endo/lysosomal dynamics can affect the efficacy of engineered therapeutic antibodies, including ADCs.
引用
收藏
页码:13 / 21
页数:9
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