Protection of Mice with Recombinant Influenza Virus Neuraminidase
Author(s) -
Edwin D. Kilbourne,
Barbara A. Pokorny,
Bert E. Johansson,
Ian Brett,
Youli Milev,
James T. Matthews
Publication year - 2004
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/381123
Subject(s) - neuraminidase , virology , virus , recombinant dna , hemagglutinin (influenza) , biology , glycoprotein , influenza a virus , orthomyxoviridae , recombinant virus , antibody , h5n1 genetic structure , microbiology and biotechnology , immunology , medicine , infectious disease (medical specialty) , disease , covid-19 , gene , biochemistry , pathology
Contemporary influenza vaccines are standardized with respect to their content of hemagglutinin, the major virus antigen. Although the immunizing effect of viral neuraminidase--the less abundant of the 2 major surface glycoproteins--has been well documented in experimental animals, the importance of the purified recombinant protein has not yet been adequately assessed in animals or humans. We demonstrate that different lots of a baculovirus-derived recombinant N2 protein, in the absence of other influenza virus proteins, can induce neuraminidase-specific antibodies, reduce the replication of both homologous and heterovariant virus in mice, and suppress disease, as it is manifested by total body weight loss.
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