Suppr超能文献

通过咪唑并喹啉连接的纳米抗体靶向肿瘤相关巨噬细胞的复极化。

Targeted Repolarization of Tumor-Associated Macrophages via Imidazoquinoline-Linked Nanobodies.

机构信息

Lab of Cellular and Molecular Immunology Vrije Universiteit Brussel Pleinlaan 2 Brussels 1050 Belgium.

Myeloid Cell Immunology Lab VIB Center for Inflammation Research Brussels 1050 Belgium.

出版信息

Adv Sci (Weinh). 2021 Mar 8;8(10):2004574. doi: 10.1002/advs.202004574. eCollection 2021 May.

Abstract

Tumor-associated macrophages (TAMs) promote the immune suppressive microenvironment inside tumors and are, therefore, considered as a promising target for the next generation of cancer immunotherapies. To repolarize their phenotype into a tumoricidal state, the Toll-like receptor 7/8 agonist imidazoquinoline IMDQ is site-specifically and quantitatively coupled to single chain antibody fragments, so-called nanobodies, targeting the macrophage mannose receptor (MMR) on TAMs. Intravenous injection of these conjugates result in a tumor- and cell-specific delivery of IMDQ into MMR TAMs, causing a significant decline in tumor growth. This is accompanied by a repolarization of TAMs towards a pro-inflammatory phenotype and an increase in anti-tumor T cell responses. Therefore, the therapeutic benefit of such nanobody-drug conjugates may pave the road towards effective macrophage re-educating cancer immunotherapies.

摘要

肿瘤相关巨噬细胞(TAMs)促进肿瘤内部的免疫抑制微环境,因此被认为是下一代癌症免疫疗法的一个有前途的靶点。为了将其表型重极化到杀伤肿瘤状态,Toll 样受体 7/8 激动剂咪唑并喹啉 IMDQ 被特异性和定量地与单链抗体片段(称为纳米体)偶联,这些纳米体靶向 TAMs 上的巨噬细胞甘露糖受体(MMR)。这些缀合物的静脉注射导致 IMDQ 特异性地递送到 MMR TAMs 中,导致肿瘤生长显著下降。这伴随着 TAMs 向促炎表型的重极化和抗肿瘤 T 细胞反应的增加。因此,这种纳米体-药物缀合物的治疗益处可能为有效的巨噬细胞再教育癌症免疫疗法铺平道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc5/8132149/ccee5b9aef65/ADVS-8-2004574-g003.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验