SNU CBE

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

동물실험

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…

이 논문을 지원한 국가R&D 과제 (NTIS 성과)

NTIS 성과DB(2020–24)에서 DOI 매칭 없음

인접 그래프

노드 hover = 이웃 강조 · 1회 클릭 = 고정 · 고정된 노드 다시 클릭 = 페이지 이동

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교수 1

김병수

연구주제 1

Immune cells in cancer

키워드 1

암 면역치료

방법 1

동물실험