Pharmacological Polarization of Tumor‐Associated Macrophages Toward a CXCL9 Antitumor Phenotype

Author:

Enbergs Noah1ORCID,Halabi Elias A.1ORCID,Goubet Anne‐Gaëlle23ORCID,Schleyer Kelton1ORCID,Fredrich Ina R.1ORCID,Kohler Rainer H.1ORCID,Garris Christopher S.1ORCID,Pittet Mikaël J.234ORCID,Weissleder Ralph15ORCID

Affiliation:

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

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

3. AGORA Cancer Center Swiss Cancer Center Leman Lausanne 1011 Switzerland

4. Ludwig Institute for Cancer Research Lausanne 1005 Switzerland

5. Department of Systems Biology Harvard Medical School 200 Longwood Ave Boston MA 02115 USA

Abstract

AbstractTumor‐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.

Funder

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Studienstiftung des Deutschen Volkes

National Cancer Institute

Publisher

Wiley

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