Key result
Apo(a) DNA vaccine reduces neointima formation and vascular Lp(a) deposition in preclinical models.
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Lipoprotein(a) [Lp(a)] is an unique lipoprotein consisting of the glycoprotein apolipoprotein(a) [apo(a)] in low-density lipoprotein. Although Lp(a) is a well-known independent risk factor for cardiovascular disease; however, there is no drugs to decrease plasma Lp(a) level. Thus, to inhibit the biological activity of Lp(a), we developed DNA vaccine for apo(a) by the targeting to the selected 12 hydrophilic amino acids in the kringle-4 type 2 domain of apo(a). Hepatitis B virus core protein was used as an epitope carrier to enhance the immunogenicity. Intramuscular immunization with apo(a) vaccine resulted in the significant inhibition of neointima formation in carotid artery ligation model using Lp(a) transgenic mice, associated with anti-apo(a) antibody and decrease in vascular Lp(a) deposition. Overall, this study provided the first evidence that the pro-atherosclerotic actions of Lp(a) could be prevented by DNA vaccine directed against apo(a), suggesting a novel therapeutic strategy to treat cardiovascular diseases related to high Lp(a).
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Kyutoku et al. (2013) studied Cardiovascular diseases related to high Lp(a). DNA vaccine for apo(a) was evaluated on Neointima formation. Intramuscular immunization with a DNA vaccine directed against apo(a) significantly inhibited neointima formation and decreased vascular Lp(a) deposition in Lp(a) transgenic mice.
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