CD137
癌症研究
T细胞
CD3型
CD8型
医学
癌症
抗原
免疫学
免疫系统
内科学
作者
Takayuki Kamikawa,N. Kimura,Shinya Ishii,Masaru Muraoka,Tatsushi Kodama,Kenji Taniguchi,Moe Yoshimoto,Momoko Miura-Okuda,Ryo Uchikawa,Chie Kato,Junko Shinozuka,S. Akai,Sotaro Naoi,Nobumoto Tomioka,Nishiki Nagaya,Chai Ling Pang,Gupta Garvita,Shu Feng,M. Shimada,Mika Kamata‐Sakurai,Hiroyuki Aburatani,Takehisa Kitazawa,Tomoyuki Igawa
标识
DOI:10.1136/jitc-2024-009563
摘要
Ovarian cancer remains a formidable challenge in oncology, necessitating innovative therapeutic approaches. Claudin-6 (CLDN6), a member of the tight junction molecule CLDN family, exhibits negligible expression in healthy tissues but displays aberrant upregulation in various malignancies, including ovarian cancer. Although several therapeutic modalities targeting CLDN6 are currently under investigation, there is still a need for more potent therapeutic options. While T-cell engagers (TCEs) hold substantial promise as potent immunotherapeutic agents, their current efficacy and safety in terms of target antigen selection and T-cell exhaustion due to only CD3 stimulation without co-stimulation must be improved, particularly against solid tumors. To provide an efficacious treatment option for ovarian cancer, we generated SAIL66, a tri-specific antibody against CLDN6/CD3/CD137.
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