Nanotechnology Research Center, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad 91775-1365, Iran.
Department of Pharmacodynamy and Toxicology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran.
Biomed Pharmacother. 2016 Jul;81:468-473. doi: 10.1016/j.biopha.2016.04.035. Epub 2016 Apr 30.
To evaluate atheroprotective effects of different doses of cholesteryl ester transfer protein (CETP) vaccine, three doses of Tetanus toxoid-CETP (TT-CETP) peptide including 10, 50 and 100/rabbit, termed FA10, FA50, FA100, respectively, were administered in rabbit model of atherosclerosis.
Animals were vaccinated subcutaneously (S.C.) with 100μl of vaccine in presence of complete Freund's adjuvant (CFA) for the first administration. Rabbits were boosted 4 times at 3 weeks intervals with the same peptide dose formulated in incomplete Freund's adjuvant (IFA). Animals were fed with diet supplemented with 2% cholesterol from week 11 to week 19. Anti-TT-CETP specific antibody and CETP activity in sera were determined. Therapeutic response was examined by tracking plasma lipoprotein levels (HDL-C, LDL-C and total cholesterol), and pathologic observation of intima/media thickness at the site of aortic lesions.
All TT-CETP vaccine doses generated strong anti TT-CETP antibody response. CETP activity reduced in rabbits vaccinated with FA100 (P=0.031). FA100 showed significant increase in level of HDL-C rather than control group (P=0.006). However, no significant reduction were found in atherosclerotic lesion when compared to control.
Inhibition of CETP activity and increased HDL-C were found with FA100, but the vaccine failed to prevent aortic lesion development in immunized rabbits when compared to control. Our result supports the hypothesis stated that CETP may not be an attractive therapeutic target for the prevention of cardiovascular disease.
评估不同剂量的胆固醇酯转移蛋白(CETP)疫苗的动脉保护作用,将三种破伤风类毒素-CETP(TT-CETP)肽疫苗(每只兔子分别给予 10、50 和 100μg,分别称为 FA10、FA50 和 FA100)用于动脉粥样硬化兔模型。
动物用完全弗氏佐剂(CFA)皮下(S.C.)接种 100μl 疫苗进行首次免疫。兔子在第 3 周间隔用相同剂量的肽在不完全弗氏佐剂(IFA)中加强免疫 4 次。从第 11 周到第 19 周,动物用补充有 2%胆固醇的饮食喂养。测定血清中抗 TT-CETP 特异性抗体和 CETP 活性。通过跟踪脂蛋白水平(HDL-C、LDL-C 和总胆固醇)和主动脉病变部位内膜/中膜厚度的病理观察来检查治疗反应。
所有 TT-CETP 疫苗剂量均产生强烈的抗 TT-CETP 抗体反应。FA100 组 CETP 活性降低(P=0.031)。FA100 组 HDL-C 水平显著升高(P=0.006),而与对照组相比无显著差异。然而,与对照组相比,动脉粥样硬化病变无明显减少。
FA100 可抑制 CETP 活性并增加 HDL-C,但与对照组相比,该疫苗未能预防免疫兔子的主动脉病变发展。我们的结果支持这样一种假设,即 CETP 可能不是预防心血管疾病的有吸引力的治疗靶点。