Your browser doesn't support javascript.
loading
Pharmacological Polarization of Tumor-Associated Macrophages Toward a CXCL9 Antitumor Phenotype.
Enbergs, Noah; Halabi, Elias A; Goubet, Anne-Gaëlle; Schleyer, Kelton; Fredrich, Ina R; Kohler, Rainer H; Garris, Christopher S; Pittet, Mikaël J; Weissleder, Ralph.
Affiliation
  • Enbergs N; Center for Systems Biology, Massachusetts General Hospital, 185 Cambridge St, CPZN 5206, Boston, MA, 02114, USA.
  • Halabi EA; Center for Systems Biology, Massachusetts General Hospital, 185 Cambridge St, CPZN 5206, Boston, MA, 02114, USA.
  • Goubet AG; Department of Pathology and Immunology, University of Geneva, Geneva, 1211, Switzerland.
  • Schleyer K; AGORA Cancer Center, Swiss Cancer Center Leman, Lausanne, 1011, Switzerland.
  • Fredrich IR; Center for Systems Biology, Massachusetts General Hospital, 185 Cambridge St, CPZN 5206, Boston, MA, 02114, USA.
  • Kohler RH; Center for Systems Biology, Massachusetts General Hospital, 185 Cambridge St, CPZN 5206, Boston, MA, 02114, USA.
  • Garris CS; Center for Systems Biology, Massachusetts General Hospital, 185 Cambridge St, CPZN 5206, Boston, MA, 02114, USA.
  • Pittet MJ; Center for Systems Biology, Massachusetts General Hospital, 185 Cambridge St, CPZN 5206, Boston, MA, 02114, USA.
  • Weissleder R; Department of Pathology and Immunology, University of Geneva, Geneva, 1211, Switzerland.
Adv Sci (Weinh) ; 11(15): e2309026, 2024 Apr.
Article in En | MEDLINE | ID: mdl-38342608
ABSTRACT
Tumor-associated macrophages (TAM) are a diverse population of myeloid cells that are often abundant and immunosuppressive in human cancers. CXCL9Hi 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.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tumor-Associated Macrophages / Neoplasms Type of study: Risk_factors_studies Limits: Animals / Humans Language: En Journal: Adv Sci (Weinh) Year: 2024 Document type: Article Affiliation country: Estados Unidos Country of publication: Alemania

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tumor-Associated Macrophages / Neoplasms Type of study: Risk_factors_studies Limits: Animals / Humans Language: En Journal: Adv Sci (Weinh) Year: 2024 Document type: Article Affiliation country: Estados Unidos Country of publication: Alemania