Apolipoprotein A-I(Milano) (apoA-I(M)) is a natural variant of apoA-I characterized by a cysteine for arginine substitution at position 173 of the primary sequence. ApoA-I(M) carriers have much less atherosclerosis than expected from their very low plasma high-density lipoprotein (HDL) cholesterol levels, suggesting that the variant might be protective. Synthetic HDL (sHDL) made with a recombinant form of the dimeric A-I(M) (A-I(M)/A-I(M)) and phospholipids given in single or multiple injections is effective in inducing the regression of atherosclerotic plaques, preventing arterial restenosis, and limiting cardiac dysfunction after ischemia/reperfusion injury. In a phase II trial in patients with acute coronary syndromes, a short-term treatment with A-I(M)/A-I(M) sHDL caused a remarkable reduction of atheroma burden. Although at early stages of drug development, A-I(M)/A-I(M) sHDL holds vast promise for the treatment of a variety of cardiovascular diseases in humans

Recombinant apolipoprotein A-IMilano for the treatment of cardiovascular diseases / L. Calabresi, C. Sirtori, R. Paoletti, G. Franceschini. - In: CURRENT ATHEROSCLEROSIS REPORTS. - ISSN 1523-3804. - 8:2(2006), pp. 163-167. [10.1007/s11883-006-0054-4]

Recombinant apolipoprotein A-IMilano for the treatment of cardiovascular diseases

L. Calabresi
Primo
;
C. Sirtori
Secondo
;
R. Paoletti
Penultimo
;
G. Franceschini
Ultimo
2006

Abstract

Apolipoprotein A-I(Milano) (apoA-I(M)) is a natural variant of apoA-I characterized by a cysteine for arginine substitution at position 173 of the primary sequence. ApoA-I(M) carriers have much less atherosclerosis than expected from their very low plasma high-density lipoprotein (HDL) cholesterol levels, suggesting that the variant might be protective. Synthetic HDL (sHDL) made with a recombinant form of the dimeric A-I(M) (A-I(M)/A-I(M)) and phospholipids given in single or multiple injections is effective in inducing the regression of atherosclerotic plaques, preventing arterial restenosis, and limiting cardiac dysfunction after ischemia/reperfusion injury. In a phase II trial in patients with acute coronary syndromes, a short-term treatment with A-I(M)/A-I(M) sHDL caused a remarkable reduction of atheroma burden. Although at early stages of drug development, A-I(M)/A-I(M) sHDL holds vast promise for the treatment of a variety of cardiovascular diseases in humans
Settore BIO/14 - Farmacologia
2006
http://www.current-reports.com/article_frame.cfm?PubID=AT08-2-1-10&Type=Article
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/28934
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