Abrogating HIV-1 Infection via Drug-Induced Reactivation of Apoptosis
The present invention relates to compositions and methods of treating, inhibiting, or controlling HIV infection.
1 . A method of identifying a compound for treating an infection with a virus, the method comprising:
mixing a test compound with a first plurality of cells in a medium for a first period of time, the cells being infected with the virus;
culturing the cells for a second period of time; and
determining the activity level of the promoter of the virus in the cells;
wherein the activity level in the presence of the test compound, if lower than that in the absence of the test compound, indicates that the test compound is a candidate for treating the infection with the virus.
2 . The method of claim 1 , wherein the culturing step comprises (i) removing the test compound from the medium and (ii) maintaining the cells for the second period of time.
3 . The method of claim 1 , wherein the determining step is conducted by determining the transcription initiation level.
4 . The method of claim 1 , wherein the method further comprises evaluating the apoptosis level of the cells and wherein the level of apoptosis in the presence of the test compound, if higher than that in the absence of the test compound, indicates that the test compound is a candidate for treating the infection with the virus.
5 . The method of claim 1 , wherein the virus is an HIV-1 virus.
6 . The method of claim 1 , wherein the first plurality of cells are PBMCs.
7 . The method of claim 6 , wherein the method further comprises evaluating the level of IL-10 or IFN-γ in the medium or cells.
8 . The method of claim 1 , wherein the method further comprises (a) contacting the first plurality of cells or the medium with a second plurality of cells, and (b) determining the activity level of the promoter of the virus in the second plurality cells.
9 . The method of claim 1 , wherein the first period of time is 2 hours-1 month.
10 . The method of claim 1 , wherein the second period of time is up to 3 months.
11 . A method of reducing or eliminating HIV-1 rebound subsequent to treatment of an HIV-1 infected subject comprising administering an iron-chelating hydroxypyridinone (HOPO) compound to a subject infected with HIV-1 in an amount and for a time effective to reduce or eliminate the level of HIV-1 virions, followed by discontinuing administration of said iron-chelating hydroxypyridinone, whereby the level of HIV-1 virions remains reduced or eliminated for at least 4 weeks after discontinuation of administration.
12 . The method of claim 11 , wherein the level of HIV-1 virions remains reduced or eliminated for at least 12 weeks after discontinuation of administration.
13 . The method of claim 11 , where said time effective to reduce or eliminate the level of HIV-1 virions is 4 weeks.
14 . The method of claim 11 , wherein the method further comprises administering to the subject an apoptosis inducer.
15 . The method of claim 11 , wherein the iron-chelating hydroxypyridinone is selected from the group consisting 6-cyclohexyl-1-hydroxy-4-methylpyrid-2(1H)-one (ciclopirox) and 3-hydroxy-1,2-dimethylpyridin-4(1H)-one (deferiprone).
16 . An immunogenic composition comprising (i) one or more cells that have been infected with HIV-1; (ii) an iron-chelating hydroxypyridinone compound; and (iii) a pharmaceutically acceptable carrier.
17 . The immunogenic composition claim 16 , wherein the cells are peripheral blood mononuclear cells (PBMCs).
18 . The immunogenic composition claim 16 , wherein the composition further comprises an adjuvant.
19 . A method of eliciting an HIV-1-specific immune response in a subject, comprising administering to a subject in need thereof the immunogenic composition of claim 16 .
20 . The method of claim 24 , wherein the subject has been infected with HIV-1.
21 . A method of increasing resistance to HIV-1 infection in a subject, comprising (i) identifying a subject that has been, or is suspected of having been, or is expected to be, exposed to HIV-1, and (ii) administering to the subject an iron-chelating hydroxypyridinone in an amount and for a time effective to maintain or decrease the IL-10 or IFN-γ level in the subject.
22 . The method of claim 21 , wherein the method further comprises administering to the subject an apoptosis inducer.
23 . The method of claim 21 , wherein the method further comprises determining the IL-10 or IFN-γ level in the subject after the administering step.