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

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Version: Final published version
License: CC BY 4.0
Serval ID
serval:BIB_595F6F9E996C
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Pharmacological Polarization of Tumor-Associated Macrophages Toward a CXCL9 Antitumor Phenotype.
Journal
Advanced science
Author(s)
Enbergs N., Halabi E.A., Goubet A.G., Schleyer K., Fredrich I.R., Kohler R.H., Garris C.S., Pittet M.J., Weissleder R.
ISSN
2198-3844 (Electronic)
ISSN-L
2198-3844
Publication state
Published
Issued date
04/2024
Peer-reviewed
Oui
Volume
11
Number
15
Pages
e2309026
Language
english
Notes
Publication types: Journal Article
Publication Status: ppublish
Abstract
Tumor-associated macrophages (TAM) are a diverse population of myeloid cells that are often abundant and immunosuppressive in human cancers. CXCL9 <sup>Hi</sup> 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.
Keywords
Humans, Animals, Mice, Tumor-Associated Macrophages, Macrophages/metabolism, Neoplasms/pathology, Phenotype, Chemokine CXCL9/metabolism, Chemokine CXCL9/therapeutic use, CXCL9, IFNg, PARP7, STING, macrophage, nanoparticles, polarization
Pubmed
Web of science
Open Access
Yes
Create date
15/02/2024 17:52
Last modification date
23/04/2024 7:11
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