M1 Macrophage-Derived Nanovesicles Potentiate the Anticancer Efficacy of Immune Checkpoint Inhibitors
2018 · ACS Nano
저자
Yeon Woong Choo, Mikyung Kang, Han Young Kim, Jin Han, Seokyung Kang, Ju‐Ro Lee, Gun‐Jae Jeong, Sung Pil Kwon, Seuk Young Song, Seokhyeong Go, Mungyo Jung, Jihye Hong, 김병수 (Byung‐Soo Kim)
연구주제
Immune cells in cancer · Extracellular vesicles in disease · Cancer Immunotherapy and Biomarkers
NTIS 과학기술표준분류
가장 가까운 분류(보건의료 > 신약·의약품개발 > 약물전달시스템)가 화학·화공 범위 밖이다. 배정 근거: AI 키워드가 잡은 NTIS 과제의 분류.
AI 연구 키워드·방법
암 면역치료 immune checkpoint inhibitor macrophage derived nanovesicle tumor associated macrophage
키워드 (OpenAlex)
tumor-associated macrophages M1 macrophages immune checkpoint inhibitors PD-L1 inhibitors tumor microenvironment cancer immunotherapy combination therapy tumor growth inhibition
초록
Cancer immunotherapy modulates immune cells to induce antitumor immune responses. Tumors employ immune checkpoints to evade immune cell attacks. Immune checkpoint inhibitors such as anti-PD-L1 antibody (aPD-L1), which is being used clinically for cancer treatments, can block immune checkpoints so that the immune system can attack tumors. However, immune checkpoint inhibitor therapy may be hampered by polarization of macrophages within the tumor microenvironment (TME) into M2 tumor-associated macrophages (TAMs), which suppress antitumor immune responses and promote tumor growth by releasing anti-inflammatory cytokines and angiogenic factors. In this study, we used exosome-mimetic nanovesicles derived from M1 macrophages (M1NVs) to repolarize M2 TAMs to M1 macrophages that release pro-inflammatory cytokines and induce antitumor immune responses and investigated whether the macrophage repol…
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