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Safety and Immunogenicity of 26-Valent Group A Streptococcus Vaccine in Healthy Adult Volunteers
Author(s) -
Shelly McNeil,
Scott A. Halperin,
Joanne M. Langley,
B R Smith,
Andrew E. Warren,
Geoffrey P. Sharratt,
Darlene Baxendale,
Mark A. Reddish,
Minhua Hu,
Steven D. Stroop,
Joel Linden,
Louis Fries,
Peter Vink,
James B. Dale
Publication year - 2005
Publication title -
clinical infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.44
H-Index - 336
eISSN - 1537-6591
pISSN - 1058-4838
DOI - 10.1086/444458
Subject(s) - immunogenicity , medicine , reactogenicity , antibody , antigen , streptococcus pyogenes , streptococcus , immunology , antibody titer , pharyngitis , antibody opsonization , microbiology and biotechnology , titer , virology , biology , staphylococcus aureus , bacteria , genetics , opsonin
Group A streptococcus (GAS) causes illness ranging from uncomplicated pharyngitis to life-threatening necrotizing fasciitis, toxic shock, and rheumatic fever. Attempts to develop an M protein-based vaccine have been hindered by the fact that some M proteins elicit both protective antibodies and antibodies that cross-react with human tissues. New molecular techniques have allowed the previous obstacles to be largely overcome.

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