Skip to main content
. 2022 Mar 16;23(6):3218. doi: 10.3390/ijms23063218

Table 1.

Pharmacological compounds targeting TME-derived factors that affect neutrophil function, currently in clinical trials. Data collected on ClinicalTrials.gov.

Target Type Name Effect on Neutrophils/MDSCs
VEGFR Blocking mAb bevacizumab Reduces MDSC recruitment into TME
Blocking mAb axitinib
c-Met and VEGFR2 inhibitor cabozantinib
GM-CSF Oncolytic virus OncoVEXGM-CSF Reduces monocyte and myeloid precursor cell numbers
Recombinant human GM-CSF sargramostim
TLR9 TLR9 agonist CMP-001 Stimulates Th1-activating cytokine production by MDSCs
TLR9 agonist SD-101
IL-12 Recombinant human IL-12 rHuIL-12 Reprograms MDSCs into APCs
IL-12 gene therapy activator veledimex
IFN-α Pegylated IFN-a pegasys Stimulates MDSC polarization
IFN-β Oncolytic Virus VSV-IFNβ-NIS Stimulates MDSC polarization
IFN-β, TGF-β mRNA Fβ2 fusokine Reprograms MDSCs in favor of CD8+ T cell responses
STAT3 STAT3 inhibitor TTI-101 Reduces immunosuppressive capacity of G-MDSCs
STAT3 inhibitor napabucasin
STAT3 inhibitor pyrimethamine
IDO1 IDO inhibitor indoximod Affects protumor granulocyte infiltration in the TME
IDO inhibitor epacadostat
IDO/TDO inhibitor linrodostat
ARG-1 Recombinant human Arg1 pegzilarginase Expression by myeloid cells is linked to protumor properties
Arg1 inhibitor INCB001158
HDAC HDAC inhibitor panobinostat Reduces MDSCs and their expression of ARG-1 and iNOS
HDAC inhibitor belinostat