TY - JOUR
T1 - Self-adjuvanting polyacrylic nanoparticulate delivery system for group A streptococcus (GAS) vaccine
AU - Zaman, Mehfuz
AU - Skwarczynski, Mariusz
AU - Malcolm, Jessica M.
AU - Urbani, Carl N.
AU - Jia, Zhongfan
AU - Batzloff, Michael R.
AU - Good, Michael F.
AU - Monteiro, Michael J.
AU - Toth, Istvan
PY - 2011/4
Y1 - 2011/4
N2 - Infection with Streptococcus pyogenes, commonly known as group A Streptococcus (GAS), is responsible for acute and postinfectious complications, including rheumatic fever and rheumatic heart disease (RHD). RHD is a global health burden, and Australia's indigenous population has one of the highest incidences of RHD worldwide. A potential peptide (J14) vaccine candidate has been previously identified from the C-terminal region of the M protein. However, such peptide-based vaccine development is hampered by a lack of carriers and adjuvants suitable for humans use. We have developed a fully synthetic peptide subunit vaccine candidate based on polyacrylate dendritic polymer. Intranasal administration of this nanoparticulate construct without additional adjuvant induced J14-specific IgG, which was also capable of in vitro opsonization of GAS, highlighting the potential of self-adjuvanting polyacrylate nanoparticle-based construct as a peptide vaccine delivery platform that may afford promising opportunities for treating systemic GAS infection. From the Clinical Editor: Polyacrylate dendrimers offer a unique approach to a nasally administered vaccine for addressing rheumatic heart disease. This paper describes the delivery of the J14 peptide, a C-terminal derivative of M-protein in group A Streptococcus.
AB - Infection with Streptococcus pyogenes, commonly known as group A Streptococcus (GAS), is responsible for acute and postinfectious complications, including rheumatic fever and rheumatic heart disease (RHD). RHD is a global health burden, and Australia's indigenous population has one of the highest incidences of RHD worldwide. A potential peptide (J14) vaccine candidate has been previously identified from the C-terminal region of the M protein. However, such peptide-based vaccine development is hampered by a lack of carriers and adjuvants suitable for humans use. We have developed a fully synthetic peptide subunit vaccine candidate based on polyacrylate dendritic polymer. Intranasal administration of this nanoparticulate construct without additional adjuvant induced J14-specific IgG, which was also capable of in vitro opsonization of GAS, highlighting the potential of self-adjuvanting polyacrylate nanoparticle-based construct as a peptide vaccine delivery platform that may afford promising opportunities for treating systemic GAS infection. From the Clinical Editor: Polyacrylate dendrimers offer a unique approach to a nasally administered vaccine for addressing rheumatic heart disease. This paper describes the delivery of the J14 peptide, a C-terminal derivative of M-protein in group A Streptococcus.
KW - Dendrimer
KW - Group A Streptococcus
KW - Intranasal immunization
KW - Self-adjuvanting vaccine
KW - Self-assembled nanoparticles
UR - http://www.scopus.com/inward/record.url?scp=79952747701&partnerID=8YFLogxK
U2 - 10.1016/j.nano.2010.10.002
DO - 10.1016/j.nano.2010.10.002
M3 - Article
C2 - 21034860
AN - SCOPUS:79952747701
SN - 1549-9634
VL - 7
SP - 168
EP - 173
JO - Nanomedicine: Nanotechnology, Biology, and Medicine
JF - Nanomedicine: Nanotechnology, Biology, and Medicine
IS - 2
ER -