Poly(hydrophobic amino acid)-Based Self-Adjuvanting Nanoparticles for Group A Streptococcus Vaccine Delivery

被引:39
作者
Azuar, Armira [1 ]
Li, Zhuoqing [1 ]
Shibu, Mohini A. [1 ]
Zhao, Lili [1 ]
Luo, Yacheng [1 ]
Shalash, Ahmed O. [1 ]
Khalil, Zeinab G. [2 ]
Capon, Robert J. [2 ]
Hussein, Waleed M. [1 ]
Toth, Istvan [3 ,4 ]
Skwarczynski, Mariusz [1 ]
机构
[1] Univ Queensland, Sch Chem & Mol Biosci, St Lucia, Qld 4072, Australia
[2] Univ Queensland, Inst Mol Biosci, St Lucia, Qld 4072, Australia
[3] Univ Queensland, Sch Chem & Mol Biosci, Inst Mol Biosci, St Lucia, Qld 4072, Australia
[4] Univ Queensland, Sch Pharm, St Lucia, Qld 4072, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
D O I
10.1021/acs.jmedchem.0c01660
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Peptide antigens have been widely used in the development of vaccines, especially for those against auto-immunity-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.
引用
收藏
页码:2648 / 2658
页数:11
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