Method of suppressing human immunodeficiency virus (HIV) replication in a subject by administering a liver X receptor (LXR) agonist
The present invention provides novel methods for treating and preventing coronary artery disease in HIV-1-infected individuals by interfering with Nef-mediated effect on ABCA1. The invention further provides novel methods for suppressing HIV infection by stimulating cholesterol efflux from cells by stimulating expression of ABCA1 in HIV-1-infected individuals. These methods take advantage of the finding that Nef, a regulatory protein of HIV-1, (1) diminishes expression of ATP-binding cassette transporter A1 (ABCA1), the main transporter of cholesterol from cells to extracellular acceptors; and (2) impairs cholesterol efflux from HIV-1-infected macrophages leading to cholesterol accumulation and formation of foam cells, which is a characteristic feature of atherosclerosis.
1. A method of suppressing HIV replication in an individual infected with human immunodeficiency virus (HIV) comprising administering to the individual an effective amount of a Liver X receptor (LXR) agonist comprising TO-901317, wherein the LXR agonist prevents cholesterol delivery and incorporation into HIV by stimulation of expression of ATP binding cassette transporter A1 (ABCA1).
2. The method of claim 1 , wherein the stimulation of expression of ABCA1 reduces HIV control of cholesterol trafficking in infected cells and stimulates efflux of cholesterol from the infected cells to extracellular molecules.
3. The method of claim 2 , wherein the extracellular molecule comprises apo A-1 or a fragment thereof.
4. The method of claim 3 wherein apo A-1 comprises a Nef targeting molecule.
5. The method of claim 1 , wherein the HIV comprises HIV-1.