US20240238409
2024-07-18
Human necessities
A61K39/215
Multi-epitope vaccines are designed to target viral pathogens, specifically SARS-CoV-2, by incorporating or expressing multiple concatemers of epitopes derived from the virus. These vaccines aim to include epitopes from conserved viral proteins, ensuring a broader immune response. A significant focus is placed on expressing epitopes that can interact with all major histocompatibility complex (MHC) I and II alleles present in more than 1% of the target population, enhancing their effectiveness across diverse genetic backgrounds.
Current vaccines for SARS-CoV-2 primarily target the spike protein, which has shown high variability and mutation rates. This leads to concerns regarding their long-term efficacy and ability to immunize all individuals due to HLA variability. The spike protein has demonstrated limited antibody response in survivors, making it a less ideal target for universal vaccination strategies.
The human immune system's response to SARS-CoV-2 is significantly influenced by HLA molecules that present viral peptides to T-cells. HLA genes are highly polymorphic, meaning individuals may respond differently to the same vaccine based on their specific HLA alleles. Understanding these variations is crucial in developing effective vaccination strategies that can account for individual genetic differences and improve overall vaccine efficacy.
Epitope-based vaccines utilize short immunogenic peptide sequences that are recognized by T-cells. These vaccines offer several advantages over traditional methods, as they do not contain live pathogens and can be tailored to accommodate genetic variations in both the virus and the population's HLA profiles. The development process leverages advanced bioinformatics and machine-learning techniques for precise epitope prediction, facilitating the creation of effective vaccine candidates.
Various platforms are being explored for delivering these multi-epitope vaccines, including nucleic acid-based approaches. One promising method is the SAM (self-amplifying mRNA) platform, which allows for efficient expression of antigens with minimal doses required. This approach enhances safety and reduces production time compared to traditional vaccine development methods, making it a viable solution for addressing emerging infectious diseases like COVID-19.