Methods for generating macrophages with enhanced cancer phagocytosis
The present invention relates to compositions and methods variously useful in treating cancer, inhibiting graft rejection, and treating autoimmune disease. The compositions and methods include those in which macrophages are conditioned to down regulate or upregulate the expression or activity of SIRPα or its interaction with CD47.
1. A method of generating macrophages with enhanced cancer phagocytosis, the method comprising:
(a) providing a biological sample from a subject, wherein the biological sample comprises macrophages;
(b) exposing the sample to an effective amount of a first composition comprising at least 100 units/ml IFNγ to suppress the expression or activity of signal regulatory protein α (SIRPα); and
(c) exposing the sample from step (b) to an effective amount of a second composition that activates Protein kinase C (PKC)-Spleen tyrosine kinase (Syk) pathway, thereby generating macrophages with enhanced cancer phagocytosis.
2. The method of claim 1 , wherein the biological sample further comprises cancer cells.
3. The method of claim 1 , wherein the biological sample further comprises dendritic cells.
4. The method of claim 1 , wherein the biological sample has been enriched for myeloid cells.
5. The method of claim 1 , wherein the first composition further comprises a Toll-like receptor (TLR) ligand.
6. The method of claim 5 , wherein the TLR ligand comprises a CpG oligonucleotide or a polyinosinic:polycytidylic acid (poly I:C).
7. The method of claim 5 , wherein the TLR ligand comprises GARDIQUIMOD or IMIQUIMOD.
8. The method of claim 1 , wherein the first composition further comprises, IL-6.
9. The method of claim 1 , wherein the first composition comprises a Toll-like receptor (TLR) ligand, IFNγ, and IL-6.
10. The method of claim 1 , wherein the second composition comprises phorbol 12-myristate 13-acetate (PMA).
11. The method of claim 1 , further comprising administering the macrophages with enhanced cancer phagocytosis to a subject.