Poly(hydrophobic amino acid)-Based Self-Adjuvanting Nanoparticles for Group A Streptococcus Vaccine Delivery.
Armira AzuarZhuoqing LiMohini A ShibuLili ZhaoYacheng LuoAhmed O ShalashZeinab G KhalilRobert J CaponWaleed M HusseinIstvan TothMariusz SkwarczynskiPublished in: Journal of medicinal chemistry (2021)
Peptide antigens have been widely used in the development of vaccines, especially for those against autoimmunity-inducing pathogens and cancers. However, peptide-based vaccines require adjuvant and/or a delivery system to stimulate desired immune responses. Here, we explored the potential of self-adjuvanting poly(hydrophobic amino acids) (pHAAs) to deliver peptide-based vaccine against Group A Streptococcus (GAS). We designed and synthesized self-assembled nanoparticles with a variety of conjugates bearing a peptide antigen (J8-PADRE) and polymerized hydrophobic amino acids to evaluate the effects of structural arrangement and pHAAs properties on a system's ability to induce humoral immune responses. Immunogenicity of the developed conjugates was also compared to commercially available human adjuvants. We found that a linear conjugate bearing J8-PADRE and 15 copies of leucine induced equally effective, or greater, immune responses than commercial adjuvants. Our fully defined, adjuvant-free, single molecule-based vaccine induced the production of antibodies capable of killing GAS bacteria.
Keyphrases
- immune response
- amino acid
- single molecule
- dendritic cells
- high glucose
- endothelial cells
- early stage
- ionic liquid
- diabetic rats
- cancer therapy
- toll like receptor
- candida albicans
- room temperature
- biofilm formation
- atomic force microscopy
- risk assessment
- oxidative stress
- inflammatory response
- aqueous solution
- living cells
- cystic fibrosis
- induced pluripotent stem cells
- climate change