Suppr超能文献

肿瘤相关巨噬细胞向 CXCL9 抗肿瘤表型的药理学极化。

Pharmacological Polarization of Tumor-Associated Macrophages Toward a CXCL9 Antitumor Phenotype.

机构信息

Center for Systems Biology, Massachusetts General Hospital, 185 Cambridge St, CPZN 5206, Boston, MA, 02114, USA.

Department of Pathology and Immunology, University of Geneva, Geneva, 1211, Switzerland.

出版信息

Adv Sci (Weinh). 2024 Apr;11(15):e2309026. doi: 10.1002/advs.202309026. Epub 2024 Feb 11.

Abstract

Tumor-associated macrophages (TAM) are a diverse population of myeloid cells that are often abundant and immunosuppressive in human cancers. CXCL9 TAM has recently been described to have an antitumor phenotype and is linked to immune checkpoint response. Despite the emerging understanding of the unique antitumor TAM phenotype, there is a lack of TAM-specific therapeutics to exploit this new biological understanding. Here, the discovery and characterization of multiple small-molecule enhancers of chemokine ligand 9 (CXCL9) and their targeted delivery in a TAM-avid systemic nanoformulation is reported. With this strategy, it is efficient encapsulation and release of multiple drug loads that can efficiently induce CXCL9 expression in macrophages, both in vitro and in vivo in a mouse tumor model. These observations provide a window into the molecular features that define TAM-specific states, an insight a novel therapeutic anticancer approach is used to discover.

摘要

肿瘤相关巨噬细胞(TAM)是一类丰富且具有免疫抑制作用的髓系细胞,在人类癌症中通常较为丰富。最近发现趋化因子配体 9(CXCL9)TAM 具有抗肿瘤表型,并与免疫检查点反应有关。尽管人们对独特的抗肿瘤 TAM 表型有了新的认识,但缺乏针对 TAM 的治疗方法来利用这一新的生物学认识。在这里,报道了多种趋化因子配体 9(CXCL9)小分子增强剂的发现和特性及其在 TAM 亲和性全身纳米制剂中的靶向递送。通过这种策略,可以有效地包封和释放多种药物负荷,从而有效地诱导巨噬细胞中 CXCL9 的表达,无论是在体外还是在小鼠肿瘤模型体内。这些观察结果为定义 TAM 特异性状态的分子特征提供了一个窗口,这是一种新的抗癌治疗方法的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96bf/11022742/7c9558d560fe/ADVS-11-2309026-g007.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验