Table 1. Clinical and experimental therapeutic approaches targeting TAMs.
Mechanism of intervention | Target | Strategy | Reference |
---|---|---|---|
Interference with TAM survival | Legumain | Legumain-based DNA vaccine | [13] |
CD204 | Anti-204 immunotoxin | [61] | |
IL4Rα/CD124 | RNA aptamer | [14] | |
CD52 | Alemtuzumab▲ | [100] | |
FRβ | Anti-FRβ mAb | [63] | |
Cytotoxicity in monocytes | Trabectedin (ET-743) ▲ | [58–60] | |
Liposomal clodronate | |||
M2pep | |||
Inhibition of macrophage recruitment | CCL2/CCR2 | Neutralizing antibody CNTO 888 | [49–52, 69] |
CCL2 inhibitor bindarit | |||
CCR2 kinase antagonist PF-04136309▲ | |||
Luteolin | |||
CSF1/CSF1R | Neutralizing antibody RG7155 | [64–67] | |
CSF-1R inhibitor PLX6134, GW2580 or PLX3397 | |||
Liposomal bisphosphonate | |||
miR-26a | |||
Repolarization of M2-like TAMs towards an M1-like phenotype | CSF1/CSF1R | CSF-1R inhibitor BLZ945 | [53] |
Microenvironmental stimuli | IL12 | [36, 48, 71–75] | |
IFN-γ | |||
polyl:C | |||
bacteria-mediated tumor therapy | |||
Vascular normalization | Zoledronic acid▲ | [76–79] | |
Histidine-rich glycoprotein | |||
Hydrazinocurcumin | |||
DMXAA▲ | |||
NF-κB pathway | TLR agonists (polyl:C, CpG-ODN, TLR9 ligand, IL10R mAb) | [12, 81–84, 101] | |
PA-MSHA | |||
Flavone glycoside Baicalin | |||
CD40 mAb | |||
Natural compound corosolic acid | |||
MAPK/ERK pathway | CuNG | [85] | |
Epigenetic regulation | Overexpressing miR-155/miR-511-3P | [87–89, 102] | |
Deletion of miR-146a | |||
Nanoparticle and liposome-based drug delivery systems | Engulfed by TAMs and subsequently target cancer cells | Mitoxantrone-loaded SLNsCisplatin-and cyclodextrin-loaded polymer nanoparticlesAlbumin nanoparticle–based Abraxane ▲Liposomal Doxil | [92, 93] |
▲Clinically feasible