HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Broadly neutralizing DNA vaccine with specific mutation alters the antigenicity and sugar-binding activities of influenza hemagglutinin.

Abstract
The rapid genetic drift of influenza virus hemagglutinin is an obstacle to vaccine efficacy. Previously, we found that the consensus hemagglutinin DNA vaccine (pCHA5) can only elicit moderate neutralization activities toward the H5N1 clade 2.1 and clade 2.3 viruses. Two approaches were thus taken to improve the protection broadness of CHA5. The first one was to include certain surface amino acids that are characteristic of clade 2.3 viruses to improve the protection profiles. When we immunized mice with CHA5 harboring individual mutations, the antibodies elicited by CHA5 containing P157S elicited higher neutralizing activity against the clade 2.3 viruses. Likewise, the viruses pseudotyped with hemagglutinin containing 157S became more susceptible to neutralization. The second approach was to update the consensus sequence with more recent H5N1 strains, generating a second-generation DNA vaccine pCHA5II. We showed that pCHA5II was able to elicit higher cross-neutralization activities against all H5N1 viruses. Comparison of the neutralization profiles of CHA5 and CHA5II, and the animal challenge studies, revealed that CHA5II induced the broadest protection profile. We concluded that CHA5II combined with electroporation delivery is a promising strategy to induce antibodies with broad cross-reactivities against divergent H5N1 influenza viruses.
AuthorsMing-Wei Chen, Hsin-Yu Liao, Yaoxing Huang, Jia-Tsrong Jan, Chih-Cheng Huang, Chien-Tai Ren, Chung-Yi Wu, Ting-Jen Rachel Cheng, David D Ho, Chi-Huey Wong
JournalProceedings of the National Academy of Sciences of the United States of America (Proc Natl Acad Sci U S A) Vol. 108 Issue 9 Pg. 3510-5 (Mar 01 2011) ISSN: 1091-6490 [Electronic] United States
PMID21321237 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Amino Acids
  • Antigens, Viral
  • Hemagglutinin Glycoproteins, Influenza Virus
  • Immune Sera
  • Influenza Vaccines
  • Polysaccharides
  • Receptors, Virus
  • Vaccines, DNA
Topics
  • Amino Acid Sequence
  • Amino Acids (genetics)
  • Animals
  • Antigens, Viral (immunology)
  • Carbohydrate Metabolism (immunology)
  • Cell Line
  • Cross Protection (immunology)
  • Hemagglutinin Glycoproteins, Influenza Virus (chemistry, immunology)
  • Humans
  • Immune Sera (immunology)
  • Influenza A Virus, H5N1 Subtype (immunology)
  • Influenza Vaccines (immunology)
  • Mice
  • Mice, Inbred BALB C
  • Microarray Analysis
  • Molecular Sequence Data
  • Mutation (genetics)
  • Neutralization Tests
  • Orthomyxoviridae Infections (immunology, prevention & control, virology)
  • Polysaccharides (metabolism)
  • Protein Structure, Tertiary
  • Receptors, Virus (metabolism)
  • Vaccines, DNA (genetics, immunology)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: