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Design of an HA2-based Escherichia coli expressed influenza immunogen that protects mice from pathogenic challenge
by
Casimiro, Danilo R.
, Lu, Xianghan
, Citron, Michael P.
, Joyce, Joseph G.
, Kim, Peter S.
, Hepler, Robert W.
, Heidecker, Gwendolyn J.
, Najar, Tariq Ahmad
, Liang, Xiaoping
, Varadarajan, Raghavan
, Bommakanti, Gayathri
, Meulen, Jan ter
, Shiver, John W.
, Callahan, Cheryl
in
Animals
/ Antibodies
/ Antibodies, Neutralizing - immunology
/ Antibodies, Viral - immunology
/ Antigens
/ Bacterial proteins
/ Binding Sites
/ Biological Sciences
/ Biophysics
/ Circular Dichroism
/ Disulfides
/ E coli
/ Escherichia coli
/ Escherichia coli - genetics
/ Escherichia coli - metabolism
/ Female
/ Gene expression
/ Genetic drift
/ Genetic mutation
/ genetic variation
/ Hemagglutinin Glycoproteins, Influenza Virus - chemistry
/ Hemagglutinin Glycoproteins, Influenza Virus - genetics
/ Hemagglutinin Glycoproteins, Influenza Virus - immunology
/ Hemagglutinin Glycoproteins, Influenza Virus - metabolism
/ Hydrogen-Ion Concentration
/ immune response
/ Immunogenicity
/ Inclusion bodies
/ Infection
/ Influenza
/ Influenza A virus - immunology
/ Influenza Vaccines - immunology
/ Mice
/ Mice, Inbred BALB C
/ Models, Molecular
/ Molecules
/ Mutation
/ neutralization
/ neutralizing antibodies
/ Orthomyxoviridae
/ Orthomyxoviridae Infections - immunology
/ Orthomyxoviridae Infections - prevention & control
/ pandemic
/ Pandemics
/ pH effects
/ Pressure
/ Protein Structure, Quaternary
/ Protein Structure, Tertiary
/ Public health
/ Receptors
/ Regional identity
/ Rodents
/ Vaccination
/ Vaccines
/ Viruses
2010
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Design of an HA2-based Escherichia coli expressed influenza immunogen that protects mice from pathogenic challenge
by
Casimiro, Danilo R.
, Lu, Xianghan
, Citron, Michael P.
, Joyce, Joseph G.
, Kim, Peter S.
, Hepler, Robert W.
, Heidecker, Gwendolyn J.
, Najar, Tariq Ahmad
, Liang, Xiaoping
, Varadarajan, Raghavan
, Bommakanti, Gayathri
, Meulen, Jan ter
, Shiver, John W.
, Callahan, Cheryl
in
Animals
/ Antibodies
/ Antibodies, Neutralizing - immunology
/ Antibodies, Viral - immunology
/ Antigens
/ Bacterial proteins
/ Binding Sites
/ Biological Sciences
/ Biophysics
/ Circular Dichroism
/ Disulfides
/ E coli
/ Escherichia coli
/ Escherichia coli - genetics
/ Escherichia coli - metabolism
/ Female
/ Gene expression
/ Genetic drift
/ Genetic mutation
/ genetic variation
/ Hemagglutinin Glycoproteins, Influenza Virus - chemistry
/ Hemagglutinin Glycoproteins, Influenza Virus - genetics
/ Hemagglutinin Glycoproteins, Influenza Virus - immunology
/ Hemagglutinin Glycoproteins, Influenza Virus - metabolism
/ Hydrogen-Ion Concentration
/ immune response
/ Immunogenicity
/ Inclusion bodies
/ Infection
/ Influenza
/ Influenza A virus - immunology
/ Influenza Vaccines - immunology
/ Mice
/ Mice, Inbred BALB C
/ Models, Molecular
/ Molecules
/ Mutation
/ neutralization
/ neutralizing antibodies
/ Orthomyxoviridae
/ Orthomyxoviridae Infections - immunology
/ Orthomyxoviridae Infections - prevention & control
/ pandemic
/ Pandemics
/ pH effects
/ Pressure
/ Protein Structure, Quaternary
/ Protein Structure, Tertiary
/ Public health
/ Receptors
/ Regional identity
/ Rodents
/ Vaccination
/ Vaccines
/ Viruses
2010
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Design of an HA2-based Escherichia coli expressed influenza immunogen that protects mice from pathogenic challenge
by
Casimiro, Danilo R.
, Lu, Xianghan
, Citron, Michael P.
, Joyce, Joseph G.
, Kim, Peter S.
, Hepler, Robert W.
, Heidecker, Gwendolyn J.
, Najar, Tariq Ahmad
, Liang, Xiaoping
, Varadarajan, Raghavan
, Bommakanti, Gayathri
, Meulen, Jan ter
, Shiver, John W.
, Callahan, Cheryl
in
Animals
/ Antibodies
/ Antibodies, Neutralizing - immunology
/ Antibodies, Viral - immunology
/ Antigens
/ Bacterial proteins
/ Binding Sites
/ Biological Sciences
/ Biophysics
/ Circular Dichroism
/ Disulfides
/ E coli
/ Escherichia coli
/ Escherichia coli - genetics
/ Escherichia coli - metabolism
/ Female
/ Gene expression
/ Genetic drift
/ Genetic mutation
/ genetic variation
/ Hemagglutinin Glycoproteins, Influenza Virus - chemistry
/ Hemagglutinin Glycoproteins, Influenza Virus - genetics
/ Hemagglutinin Glycoproteins, Influenza Virus - immunology
/ Hemagglutinin Glycoproteins, Influenza Virus - metabolism
/ Hydrogen-Ion Concentration
/ immune response
/ Immunogenicity
/ Inclusion bodies
/ Infection
/ Influenza
/ Influenza A virus - immunology
/ Influenza Vaccines - immunology
/ Mice
/ Mice, Inbred BALB C
/ Models, Molecular
/ Molecules
/ Mutation
/ neutralization
/ neutralizing antibodies
/ Orthomyxoviridae
/ Orthomyxoviridae Infections - immunology
/ Orthomyxoviridae Infections - prevention & control
/ pandemic
/ Pandemics
/ pH effects
/ Pressure
/ Protein Structure, Quaternary
/ Protein Structure, Tertiary
/ Public health
/ Receptors
/ Regional identity
/ Rodents
/ Vaccination
/ Vaccines
/ Viruses
2010
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Design of an HA2-based Escherichia coli expressed influenza immunogen that protects mice from pathogenic challenge
Journal Article
Design of an HA2-based Escherichia coli expressed influenza immunogen that protects mice from pathogenic challenge
2010
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Overview
Influenza HA is the primary target of neutralizing antibodies during infection, and its sequence undergoes genetic drift and shift in response to immune pressure. The receptor binding HA1 subunit of HA shows much higher sequence variability relative to the metastable, fusion-active HA2 subunit, presumably because neutralizing antibodies are primarily targeted against the former in natural infection. We have designed an HA2-based immunogen using a protein minimization approach that incorporates designed mutations to destabilize the low pH conformation of HA2. The resulting construct (HA6) was expressed in Escherichia coli and refolded from inclusion bodies. Biophysical studies and mutational analysis of the protein indicate that it is folded into the desired neutral pH conformation competent to bind the broadly neutralizing HA2 directed monoclonal 12D1, not the low pH conformation observed in previous studies. HA6 was highly immunogenic in mice and the mice were protected against lethal challenge by the homologous A/HK/68 mouse-adapted virus. An HA6-like construct from another H3 strain (A/Phil/2/82) also protected mice against A/HK/68 challenge. Regions included in HA6 are highly conserved within a subtype and are fairly well conserved within a clade. Targeting the highly conserved HA2 subunit with a bacterially produced immunogen is a vaccine strategy that may aid in pandemic preparedness.
Publisher
National Academy of Sciences,National Acad Sciences
Subject
/ Antibodies, Neutralizing - immunology
/ Antibodies, Viral - immunology
/ Antigens
/ E coli
/ Escherichia coli - metabolism
/ Female
/ Hemagglutinin Glycoproteins, Influenza Virus - chemistry
/ Hemagglutinin Glycoproteins, Influenza Virus - genetics
/ Hemagglutinin Glycoproteins, Influenza Virus - immunology
/ Hemagglutinin Glycoproteins, Influenza Virus - metabolism
/ Influenza A virus - immunology
/ Influenza Vaccines - immunology
/ Mice
/ Mutation
/ Orthomyxoviridae Infections - immunology
/ Orthomyxoviridae Infections - prevention & control
/ pandemic
/ Pressure
/ Protein Structure, Quaternary
/ Rodents
/ Vaccines
/ Viruses
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