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