肽
表位
抗体
癌症研究
肽疫苗
癌症
结合
单克隆抗体
抗原
抗体-药物偶联物
免疫原性
医学
免疫疗法
化学
生物
分子生物学
噬菌体展示
作者
Songfa Zhang,Chuan Yan,David G. Millar,Qiqi Yang,James M. Heather,Adam Langenbucher,Laura T. Morton,Sean Sepulveda,Eric Alpert,Lauren R. Whelton,Dominique T. Zarrella,Mei Guo,Eleanor Minogue,Michael S. Lawrence,Bo R. Rueda,David R. Spriggs,Weiguo Lu,David M. Langenau,Mark Cobbold
出处
期刊:Cancer Research
[American Association for Cancer Research]
日期:2021-12-29
卷期号:: canres.2200.2021-canres.2200.2021
标识
DOI:10.1158/0008-5472.can-21-2200
摘要
Antibody-peptide epitope conjugates (APEC) are a new class of modified antibody-drug conjugates that redirect T cell viral immunity against tumor cells. APECs contain a tumor-specific protease cleavage site linked to a patient-specific viral epitope, resulting in presentation of viral epitopes on cancer cells and subsequent recruitment and killing by CD8+ T cells. Here we developed an experimental pipeline to create patient-specific APECs and identified new preclinical therapies for ovarian carcinoma. Using functional assessment of viral peptide antigen responses to common viruses like cytomegalovirus (CMV) in ovarian cancer patients, a library of 192 APECs with distinct protease cleavage sequences was created using the anti-epithelial cell adhesion molecule (EpCAM) antibody. Each APEC was tested for in vitro cancer cell killing, and top candidates were screened for killing xenograft tumors grown in zebrafish and mice. These preclinical modeling studies identified EpCAM-MMP7-CMV APEC (EpCAM-MC) as a potential new immunotherapy for ovarian carcinoma. Importantly, EpCAM-MC also demonstrated robust T cell responses in primary ovarian carcinoma patient ascites samples. This work highlights a robust, customizable platform to rapidly develop patient-specific APECs.
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