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Strategies to Overcome Hurdles in Cancer Immunotherapy

Cited 1 time in Web of Science Cited 1 time in Scopus
Authors

Kim, Jihyun; Lee, Byung Joon; Moon, Sehoon; Lee, Hojeong; Lee, JuyongKim, Byung-Soo; Jung, Keehoon; Seo, Hyungseok; Chung, Yeonseok

Issue Date
2024-09
Publisher
The Korean Society for Biomaterials | BioMed Central
Citation
Biomaterials Research, Vol.28, p. 0080
Abstract
Despite marked advancements in cancer immunotherapy over the past few decades, there remains an urgent need to develop more effective treatments in humans. This review explores strategies to overcome hurdles in cancer immunotherapy, leveraging innovative technologies including multi-specific antibodies, chimeric antigen receptor (CAR) T cells, myeloid cells, cancer-associated fibroblasts, artificial intelligence (AI)-predicted neoantigens, autologous vaccines, and mRNA vaccines. These approaches aim to address the diverse facets and interactions of tumors' immune evasion mechanisms. Specifically, multi-specific antibodies and CAR T cells enhance interactions with tumor cells, bolstering immune responses to facilitate tumor infiltration and destruction. Modulation of myeloid cells and cancer-associated fibroblasts targets the tumor's immunosuppressive microenvironment, enhancing immunotherapy efficacy. AI-predicted neoantigens swiftly and accurately identify antigen targets, which can facilitate the development of personalized anticancer vaccines. Additionally, autologous and mRNA vaccines activate individuals' immune systems, fostering sustained immune responses against cancer neoantigens as therapeutic vaccines. Collectively, these strategies are expected to enhance efficacy of cancer immunotherapy, opening new horizons in anticancer treatment.
ISSN
1226-4601
URI
https://hdl.handle.net/10371/211228
DOI
https://doi.org/10.34133/bmr.0080
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  • College of Engineering
  • School of Chemical and Biological Engineering
Research Area biomaterials, nanomedicine, regenerative medicine

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