Cell therapy using ex vivo reprogrammed macrophages enhances antitumor immune responses in melanoma.

ABSTRACT:

Background

Macrophage-based cell therapies have shown modest success in clinical trials, which can be attributed to their phenotypic plasticity, where transplanted macrophages get reprogrammed towards a pro-tumor phenotype. In most tumor types, including melanoma, the balance between antitumor M1-like and tumor-promoting M2-like macrophages is critical in defining the local immune response with a higher M1/M2 ratio favoring antitumor immunity. Therefore, designing novel strategies to increase the M1/M2 ratio in the TME has high clinical significance and benefits macrophage-based cell therapies.

Methods

In this study, we reprogrammed antitumor and proinflammatory macrophages ex-vivo with HDAC6 inhibitors (HDAC6i). We administered the reprogrammed macrophages intratumorally as

SUBMITTER: Noonepalle SKR 

PROVIDER: S-EPMC11401321 | biostudies-literature | 2024 Sep

REPOSITORIES: biostudies-literature