Treating atherosclerosis by removing senescent foam cell macrophages from atherosclerotic plaques
Foamy macrophages with senescence markers accumulate in the subendothelial space at the onset of atherosclerosis where they drive pathology by increasing expression of key atherogenic and inflammatory cytokines and chemokines. In advanced lesions, senescent cells promote features of plaque instability, including elastic fiber degradation and fibrous cap thinning, by heightening metalloprotease production. This invention provides methods and materials for treating arthritis by removing senescent cells in or around atherosclerotic plaques, thereby stabilizing the plaques, inhibiting rupture of the plaques and pathological sequelae that manifest as coronary artery disease.
1. A method of inhibiting progression of atherosclerosis in a subject, comprising treating the subject with a course of therapy using a pharmaceutical composition that contains a senolytic compound in an amount and in a formulation that is effective in eliminating p 16 positive senescent cells from a plurality of atherosclerotic plaques in the subject,
wherein the senolytic compound constitutes a means for selectively inhibiting mouse double minute 2 homolog (MDM2),
wherein the course of therapy includes:
(1) a treatment period during which the composition is administered systemically to the subject such that the compound contacts and selectively removes senescent cells from the atherosclerotic plaques; followed by
(2) a therapeutic period of at least two weeks, during which the composition is not administered to the subject, and progression of the atherosclerosis is inhibited as a result of administration of the composition to the subject during the treatment period.
2. The method of claim 1 , wherein the compound is (4-[(4S,5R)-4,5 bis(4-chlorophenyl)-4,5-dihydro-2-[4-methoxy-2-(1-methylethoxy)phenyl]-1H-imidazol-1-yl]carbonyl]-2-piperazinone)(Nutlin-3A), or a pharmaceutically acceptable salt thereof.
3. The method of claim 1 , wherein the compound is selected from Nutlin-1, Nutlin-2, RG-7112, RG7388, DS-3032b, MI-63, MI-126, MI-122, MI-142, MI-147, MI-219, MI-220, MI-221, MI-773, 3-(4-chlorophenyl)-3-((1-(hydroxymethyl)cyclopropyl)methoxy)-2-(4-nitrobenzyl)isoindolin-1-one, Serdemetan, AM-8553, CGM097, RO-2443, RO-5963, 5-[(3S)-3-(4-chlorophenyl)-4-[(R)-1-(4-chlorophenyl)ethyl]-2,5-dioxo-7-phenyl-1,4-diazepin-1-yl]valeric acid, 5-[(3S)-7-(2-bromophenyl)-3-(4-chlorophenyl)-4-[(R)-1-(4-chlorophenypethyl]-2,5-dioxo-1,4-diazepin-1-yl]valeric acid, TDP521252, TDP665759, NSC279287, and phannaceutically acceptable salts thereof.
4. The method of claim 1 , wherein the senescent cells are senescent foam cell macrophages.
5. The method of claim 1 , wherein the amount of the compound, the formulation of the composition, and the length of the treatment period are effective in delaying coat thinning of the atherosclerotic plaques during the therapeutic period.
6. The method of claim 1 , wherein the amount of the compound, the formulation of the composition, and the length of the treatment period are effective in stabilizing the atherosclerotic plaques, thereby reducing the risk that the plaques will rupture during the therapeutic period.
7. A method of removing senescent foam cell macrophages from the vasculature of a subject in need thereof, the method comprising:
treating the subject with a course of therapy using a pharmaceutical composition that contains a senolytic compound in an amount and in a formulation that is effective in eliminating senescent foam macrophages from the vasculature of the subject,
wherein the senolytic compound constitutes a means for selectively inhibiting mouse double minute 2 homolog (MDM2),
wherein the course of therapy includes:
(1) a treatment period during which the composition is administered systemically to the subject such that the compound selectively removes senescent foam macrophages from the vasculature of the subject; followed by
(2) a therapeutic period of at least two weeks, during which the composition is not administered to the subject, and occlusion of the vasculature by plaque distribution or rupture is inhibited as a result of administration of the composition to the subject during the treatment period.
8. The method of claim 7 , wherein the compound is (4-[(4S,5R)-4,5bis(4-chlorophenyl)-4,5-dihydro-2-[4-methoxy-2-(1-methylethoxy)phenyl]-1H-imidazol-1-yl]carbonyl]-2-piperazinone)(Nutlin-3A), or a pharmaceutically acceptable salt thereof.
9. The method of claim 7 , wherein the compound is selected from Nutlin-1, Nutlin-2, RG-7112, RG7388, DS-3032b, MI-63, MI-126, MI-122, MI-142, MI-147, MI-219, MI-220, MI-221, MI-773, 3-(4-chlorophenyl)-3-((1-(hydroxymethyl)cyclopropyl)methoxy)-2-(4-nitrobenzyl)isoindolin-1-one, Serdemetan, AM-8553, CGM097, RO-2443, RO-5963, 5-[(3S)-3-(4-chlorophenyl)-4-[(R)-1-(4-chlorophenyl)ethyl]-2,5-dioxo-7-phenyl-1,4-diazepin-1-yl]valeric acid, 5-[(3S)-7-(2-bromophenyl)-3-(4-chlorophenyl)-4-[(R)-1-(4-chlorophenyl)ethyl]-2,5-dioxo-1,4-diazepin-1-yl]valeric acid, TDP521252, TDP665759, NSC279287, and pharmaceutically acceptable salts thereof.
10. The method of claim 7 , wherein the senescent foam cell macrophages are positive for p 16.
11. The method of claim 7 , wherein the amount of the compound, the formulation of the composition, and the length of the treatment period are effective in inhibiting formation of new atherosclerotic plaques in the subject during the therapeutic period.
12. The method of claim 7 , wherein the amount of the compound, the formulation of the composition, and the length of the treatment period are effective in stabilizing atherosclerotic plaques in the subject, thereby reducing the risk that the plaques will rupture during the therapeutic period.