한빛사논문
Yonghyun Choia, Jiwon Kima, Jayoung Chaea, Joohye Honga, Jongjun Parka, Eunseo Jeonga, Hayoung Kima, Masayoshi Tanakab, Mina Okochib, Jonghoon Choia,*
aSchool of Integrative Engineering, Chung-Ang University, Seoul, Republic of Korea
bDepartment of Chemical Science and Engineering, Tokyo Institute of Technology, 2-12-1-S1-24, O-okayama, Meguro-ku, Tokyo 152-8552, Japan
*Corresponding author.
Abstract
Cancer immunotherapy is an emerging therapeutic strategy for cancer treatment. Most of the immunotherapeutics approved by the FDA regulate the innate immune system and associated immune cell activity, with immune check inhibitors in particular having transformed the field of cancer immunotherapy due to their significant clinical potential. However, previously reported immunotherapeutics have exhibited undesirable side effects, including autoimmune toxicity and inflammation. Controlling these deleterious responses and designing therapeutics that can precisely target specific regions are thus crucial to improving the efficacy of cancer immunotherapies. Recent studies have reported that cancer cells employ glycan−immune checkpoint interactions to modulate immune cell activity. Thus, the recognition of cancer glycan moieties such as sialoglycans may improve the anticancer activity of immune cells. In this review, we discuss recent advances in cancer immunotherapies involving glycans and glycan-targeting technologies based on nanomaterial-assisted local delivery systems.
Keywords : Glycosylation, Cancer glycan, Cancer immunotherapy, Glycan targeting, Nanoparticle
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