| Literature DB >> 33529034 |
Armira Azuar1, Zhuoqing Li1, Mohini A Shibu1, Lili Zhao1, Yacheng Luo1, Ahmed O Shalash1, Zeinab G Khalil2, Robert J Capon2, Waleed M Hussein1, Istvan Toth1,2,3, Mariusz Skwarczynski1.
Abstract
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.Entities:
Year: 2021 PMID: 33529034 DOI: 10.1021/acs.jmedchem.0c01660
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446