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Preclinical toxicity assessment of a peptide-based antiPCSK9 vaccine in healthy mice - 13/01/23

Doi : 10.1016/j.biopha.2022.114170 
Amir Abbas Momtazi-Borojeni a, Maciej Banach b, c, Sayed Abbas Tabatabaei d, Amirhossein Sahebkar e, f, g,
a Noncommunicable Diseases Research Center, Neyshabur University of Medical Sciences, Neyshabur, Iran 
b Department of Preventive Cardiology and Lipidology, Medical University of Lodz, 93-338 Lodz, Poland 
c Cardiovascular Research Centre, University of Zielona Gora, 65-417 Zielona Gora, Poland 
d Department of Pathology, Mashhad University of Medical Sciences, Mashhad, Iran 
e Biotechnology Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran 
f Applied Biomedical Research Center, Mashhad University of Medical Sciences, Mashhad, Iran 
g Department of Biotechnology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran 

Corresponding author at: Biotechnology Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran.Biotechnology Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical SciencesMashhadIran.

Abstract

Background

Proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibition is a novel cholesterol-lowering treatment for decreasing the risk of atherosclerosis. We have previously shown that active immunization using the antiPCSK9 vaccine could decrease hypercholesterolemia and impede the development of atherosclerotic lesions in the experimental model of atherosclerosis. Here, we evaluated the toxicity of the vaccine in healthy mice.

Methods

Forty male and female albino mice were divided into 4 experimental groups, including vaccine female (10 mice) and male (10 mice) groups receiving the antiPCSK9 vaccine as well as the corresponding control female (10 mice) and male (10 mice) groups receiving the phosphate buffer. Vaccination was planned based on 4 subcutaneous injections of the vaccine formulation (10 µg/mouse) in bi-weekly intervals. The toxicity study was performed by the subacute protocol, 28 days after the last vaccine injection. To this end, the plasma levels of lipid indexes, urea, creatinine, AST, ALT, ALP, and fasting plasma glucose (FPG), as well as the CBC test were measured. To evaluate histopathological alterations, various tissues including the heart, liver, kidney, spleen, and brain were studied using hematoxylin & eosin (H&E) staining by an expert pathologist. The severity of damage to the tissue was considered based on the standard classification; grade 1 as light damage, grade 2 as moderate damage, grade 3 as near intense damage, and grade 4 as intense damage.

Results

The results showed non-significant changes of total cholesterol, LDL-C, triglyceride, HDL-C, FBS, creatinine, urea, AST, ALP, ALT, and PAB in the vaccinated mice when compared with control mice. The CBS test indicated that there were no significant changes in the levels of WBC, RBC, HGB, HCT, MCH, MCHC, PLT, LYM, NEUT, MCV, RDW-S, PDW, and MPV in the vaccinated mice when compared with control mice. Evaluating histopathological alterations in various tissues indicated no significant adverse effects in vaccinated mice when compared to control mice.

Conclusion

The findings of the present study indicate that antiPCSK9 is safe and exerts no adverse effects on the function of different organs and blood levels of cellular and biochemical biomarkers in healthy mice.

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Keywords : Antibody, Immunotherapy, PCSK9, Toxicity, Vaccine


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Article 114170- février 2023 Retour au numéro
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