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논문 기본 정보

자료유형
학술저널
저자정보
Kim Minjeong (Department of Biomedical Engineering SKKU Institute for Convergence Sungkyunkwan University (SKKU)) Lee Na Kyeong (Sungkyunkwan University) Wang Chi-Pin James (Sungkyunkwan University) Lim Jaesung (성균관대학교) 변민지 (성균관대학교) 김태형 (중앙대학교) 박우람 (성균관대학교) Park Dae-Hwan (Department of Engineering Chemistry Chungbuk National University) Kim Se-Na (Research and Development Center MediArk Inc.) 박천권 (성균관대학교)
저널정보
한국생체재료학회 생체재료학회지 생체재료학회지 제27권
발행연도
2023.3
수록면
449 - 471 (23page)
DOI
10.1186/s40824-023-00343-4

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The tumor microenvironment (TME) is a unique environment that is developed by the tumor and controlled by tumor-induced interactions with host cells during tumor progression. The TME includes immune cells, which can be classified into two types: tumor- antagonizing and tumor-promoting immune cells. Increasing the tumor treatment responses is associated with the tumor immune microenvironment. Targeting the TME has become a popular topic in research, which includes polarizing macrophage phenotype 2 into macrophage phenotype 1 using Toll-like receptor agonists with cytokines, anti-CD47, and anti-SIPRα. Moreover, inhibiting regulatory T cells through blockades and depletion restricts immunosuppressive cells in the TME. Reprogramming T cell infiltration and T cell exhaustion improves tumor infiltrating lymphocytes, such as CD8+ or CD4+ T cells. Targeting metabolic pathways, including glucose, lipid, and amino acid metabolisms, can suppress tumor growth by restricting the absorption of nutrients and adenosine triphosphate energy into tumor cells. In conclusion, these TME reprogramming strategies exhibit more effective responses using combination treatments, biomaterials, and nanoparticles. This review highlights how biomaterials and immunotherapy can reprogram TME and improve the immune activity.

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