Gadiyar Varsha, Calianese David C, Pulica Rachael, Varsanyi Christopher, Wang Ziren, Aquib Ahmed, Choudhary Alok, Birge Raymond B
Department of Microbiology, Biochemistry and Molecular Genetics, (3)Center for Cell Signaling, Rutgers New Jersey Medical School, Newark, NJ, United States.
Department of Microbiology, Biochemistry and Molecular Genetics, (3)Center for Cell Signaling, Rutgers New Jersey Medical School, Newark, NJ, United States; Laboratory of Biochemistry and Immunology, World Premier International Research Center, Immunology Frontier Research Center, Osaka University, Suita, Osaka, Japan.
Methods Cell Biol. 2025;191:15-40. doi: 10.1016/bs.mcb.2024.10.003. Epub 2024 Nov 21.
The externalization of Phosphatidylserine (PS) from the inner surface of the plasma membrane to the outer surface of the plasma membrane is an emblematic event during apoptosis and serves as a potent "eat-me" signal for the efferocytosis of apoptotic cells. Although less well understood, PS is also externalized on live cells in the tumor microenvironment and on live virus-infected cells whereby it serves as an immune modulatory signal that drives tolerance and immune escape. Given the importance of PS in cancer immunology and immune escape, PS-targeting monoclonal antibodies have been characterized with promising immunotherapeutic potential. Here, we describe the cloning and characterization of a series of PS targeting antibodies and their potential use and utility in immuno-oncology.
磷脂酰丝氨酸(PS)从质膜内表面外化至质膜外表面是细胞凋亡过程中的一个标志性事件,并且作为凋亡细胞胞葬作用的有效“吃我”信号。尽管了解较少,但PS在肿瘤微环境中的活细胞以及活的病毒感染细胞上也会外化,在此它作为一种免疫调节信号驱动免疫耐受和免疫逃逸。鉴于PS在癌症免疫学和免疫逃逸中的重要性,靶向PS的单克隆抗体已显示出有前景的免疫治疗潜力。在此,我们描述了一系列靶向PS的抗体的克隆与特性,以及它们在免疫肿瘤学中的潜在用途。