Kim Minjeong, Lee Na Kyeong, Wang Chi-Pin James, Lim Jaesung, Byun Min Ji, Kim Tae-Hyung, Park Wooram, Park Dae-Hwan, Kim Se-Na, Park Chun Gwon
Department of Biomedical Engineering, SKKU Institute for Convergence, Sungkyunkwan University (SKKU), Suwon, Gyeonggi, 16419, Republic of Korea.
Department of Intelligent Precision Healthcare Convergence, SKKU Institute for Convergence, Sungkyunkwan University (SKKU), Suwon, Gyeonggi, 16419, Republic of Korea.
Biomater Res. 2023 Jan 31;27(1):5. doi: 10.1186/s40824-023-00343-4.
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.
肿瘤微环境(TME)是一种独特的环境,它由肿瘤形成,并在肿瘤进展过程中受肿瘤诱导的与宿主细胞的相互作用所控制。TME包括免疫细胞,可分为两种类型:抗肿瘤免疫细胞和促肿瘤免疫细胞。提高肿瘤治疗反应与肿瘤免疫微环境相关。靶向TME已成为研究中的一个热门话题,其中包括使用Toll样受体激动剂与细胞因子、抗CD47和抗SIPRα将巨噬细胞表型2极化为巨噬细胞表型1。此外,通过阻断和消耗来抑制调节性T细胞可限制TME中的免疫抑制细胞。重新编程T细胞浸润和T细胞耗竭可改善肿瘤浸润淋巴细胞,如CD8或CD4 T细胞。靶向代谢途径,包括葡萄糖、脂质和氨基酸代谢,可通过限制肿瘤细胞对营养物质和三磷酸腺苷能量的吸收来抑制肿瘤生长。总之,这些TME重编程策略在联合治疗、生物材料和纳米颗粒的使用中表现出更有效的反应。本综述强调了生物材料和免疫疗法如何重编程TME并提高免疫活性。