Background: Hepatitis B is a severe overwhelming infection. Hepatitis B is a viral infection that attacks liver cells, causing inflammation and damage to the liver. Infection is usually confined to hepatocytes. Over 2 billion people have been infected with hepatitis B virus at some point. Immunity arises from natural infection or from administration of vaccines. Purpose of the survey: Development of an RNA vaccine against lethal hepatitis B surface antigen of hepatitis B virus.
Research type: screening experiment research. Methodology: In our study, we victimized bioinformatics to engineer an RNA vaccine from hepatitis B surfactant antigen. Lipid nanoparticles with a particle size of 150 nanometers were utilized as a vaccine delivery system. Result: The vaccine has shown an efficacy of 81% in preclinical animal studies and an efficacy of 79% in human clinical studies (Phase 1/2 clinical trials). It exhibited moderate biological activity and had fewer side effects than other standard vaccines. The effect lasted for a long time.
Conclusion:
Our RNA-HBV vaccine was a promising prophylactic vaccine against fatal hepatitis B virus infection.
Kassab, M. (2024). Development of lipid nano particles RNA vaccine against hepatitis B surface antigens of hepatitis B virus. International Journal of Health Sciences (Egypt), 2(2), 74-83. doi: 10.21608/ijhegy.2023.203375.1018
MLA
Mohammed M Kassab. "Development of lipid nano particles RNA vaccine against hepatitis B surface antigens of hepatitis B virus", International Journal of Health Sciences (Egypt), 2, 2, 2024, 74-83. doi: 10.21608/ijhegy.2023.203375.1018
HARVARD
Kassab, M. (2024). 'Development of lipid nano particles RNA vaccine against hepatitis B surface antigens of hepatitis B virus', International Journal of Health Sciences (Egypt), 2(2), pp. 74-83. doi: 10.21608/ijhegy.2023.203375.1018
VANCOUVER
Kassab, M. Development of lipid nano particles RNA vaccine against hepatitis B surface antigens of hepatitis B virus. International Journal of Health Sciences (Egypt), 2024; 2(2): 74-83. doi: 10.21608/ijhegy.2023.203375.1018