The Immunogenic Potential of PCSK9 Peptide Vaccine in Mice

Aim To evaluate the immunogenic potential of the carrier-free peptide-based anti-PCSK9 (proprotein convertase subtilisin/kexin 9) vaccine in albino mice. Methods The immunogenic pcsk9 peptide and 0.4% alum adjuvant were mixed thoroughly at a 1:1 ratio and used as a vaccine formulation. To assess the humoral immune response, animals' blood was sampled two weeks after the last immunization. The ELISA method was employed to measure serum anti-PCSK9 antibody titers, PCSK9 concentrations, and PCSK9/LDLR interaction. Results ELISA analysis showed significant induction of IgG antibody titers by PCSK9 peptide vaccine in vaccinated mice sera compared to the control mice (in male and female mice were 12000 +/- 586 and 11566 +/- 642, respectively, p<0.001). Mechanistic analyses showed a significant reduction in serum PCSK9 concentrations by vaccine-induced antibodies in vaccine groups compared to the control groups (in male mice by 29 +/- 5 ng/mL (22.4%), p<0.001 and female mice by 26 +/- 5 ng / mL (21.0%), p<0.001). Serum concentrations of PCSK9 in control and vaccine groups were 131 +/- 8.6 ng / mL and 102 +/- 8.1 ng/ml in male mice and 124 +/- 6 ng/ml and 98 +/- 10 ng/ml in female mice, respectively. Moreover, vaccine-induced antibodies inhibited the PCSK9-LDLR interaction in male and female groups by 34% and 26%, respectively. No significant difference was detected between the male and female groups in all tests (p>0.05). Conclusion According to our results, the PCSK9 peptide vaccine provoked the humoral immune system in albino mice to produce functional antibodies that inhibit plasma PCSK9. These effects were seen in both genders without any significant difference.

Automated summary

This study evaluated the immunogenic potential of a carrier-free peptide-based anti-PCSK9 vaccine in albino mice. The results showed that the vaccine induced a significant production of IgG antibodies and inhibited PCSK9 concentrations and its interaction with LDLR in the blood plasma.