Methods and compositions for treating cancers and enhancing therapeutic immunity by selectively reducing immunomodulatory M2 monocytes
AssigneeThomas Jefferson University
InventorsDavid W. Andrews, Douglas C. Hooper
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Abstract
The present disclosure provides pharmaceutical compositions comprising nucleic acids capable of targeting IGF-1R expression in M2 cells. The present disclosure also provides methods for the selective reduction of M2 cells by targeting expression of IGF-1R in these cells. The present disclosure further provides methods for treating cancer and enhancing therapeutic by targeting expression of IGF-1R in M2 cells in patients. The pharmaceutical composition of the present invention is effective when administered systemically to subjects in need thereof. The ease of administration of the pharmaceutical composition facilitates treatment and enhances patient compliance.
Claims24
A method for selective reduction of M2 cells in a subject suffering from glioblastoma, the method comprising systemically administering to the subject an effective amount of a pharmaceutical composition comprising an Insulin-like Growth Factor 1 Receptor antisense oligonucleotide (IGF-1R AS ODN), wherein the sequence of the IGFR-1R AS ODN is SEQ ID NO:
- 1 and wherein the IGF-1R AS ODN is administered at a dose of about 0.025 g/kg to about 0.2 g/kg;
- and further wherein the M2 cells are M2 macrophages or M2 monocytes that express one or more cell surface markers selected from CD11b, CD14, CD15, CD23, CD64, CD68, CD163, CD204 and CD206.
A method for selective reduction of M2 cells in a subject suffering from glioblastoma, the method comprising systemically administering to the subject an effective amount of a pharmaceutical composition comprising an Insulin-like Growth Factor 1 Receptor antisense oligonucleotide (IGF-1R AS ODN), wherein the sequence of the IGFR-1R AS ODN is SEQ ID NO:
- 1 and wherein the IGF-1R AS ODN is administered at a dose of about 0.025 g/kg to about 0.2 g/kg;
- and further wherein the subject has at least one M2 cell in their circulation, in a tumor microenvironment, or serum that polarizes undifferentiated monocytes towards M2 cells.
Dependencies are inferred from the claim text.