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Recombinant influenza A virus vaccines for the pathogenic human A/Hong Kong/97 (H5N1) viruses.
J Infect Dis. 1999 May; 179(5):1132-8.JI

Abstract

Recombinant reassortment technology was used to prepare H5N1 influenza vaccine strains containing a modified hemagglutinin (HA) gene and neuraminidase gene from the A/Hong Kong/156/97 and A/Hong Kong/483/97 isolates and the internal genes from the attenuated cold-adapted A/Ann Arbor/6/60 influenza virus strain. The HA cleavage site (HA1/HA2) of each H5N1 isolate was modified to resemble that of "low-pathogenic" avian strains. Five of 6 basic amino acids at the cleavage site were deleted, and a threonine was added upstream of the remaining arginine. The H5 HA cleavage site modification resulted in the expected trypsin-dependent phenotype without altering the antigenic character of the H5 HA molecule. The temperature-sensitive and cold-adapted phenotype of the attenuated parent virus was maintained in the recombinant strains, and they grew to 108.5-9.4 EID50/mL in eggs. Both H5N1 vaccine virus strains were safe and immunogenic in ferrets and protected chickens against wild-type H5N1 virus challenge.

Authors+Show Affiliations

Aviron, Mountain View, California Veterinary Diagnostic Laboratory CA System, Davis, CA, USA. sli@aviron.comNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

10191214

Citation

Li, S, et al. "Recombinant Influenza a Virus Vaccines for the Pathogenic Human A/Hong Kong/97 (H5N1) Viruses." The Journal of Infectious Diseases, vol. 179, no. 5, 1999, pp. 1132-8.
Li S, Liu C, Klimov A, et al. Recombinant influenza A virus vaccines for the pathogenic human A/Hong Kong/97 (H5N1) viruses. J Infect Dis. 1999;179(5):1132-8.
Li, S., Liu, C., Klimov, A., Subbarao, K., Perdue, M. L., Mo, D., Ji, Y., Woods, L., Hietala, S., & Bryant, M. (1999). Recombinant influenza A virus vaccines for the pathogenic human A/Hong Kong/97 (H5N1) viruses. The Journal of Infectious Diseases, 179(5), 1132-8.
Li S, et al. Recombinant Influenza a Virus Vaccines for the Pathogenic Human A/Hong Kong/97 (H5N1) Viruses. J Infect Dis. 1999;179(5):1132-8. PubMed PMID: 10191214.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Recombinant influenza A virus vaccines for the pathogenic human A/Hong Kong/97 (H5N1) viruses. AU - Li,S, AU - Liu,C, AU - Klimov,A, AU - Subbarao,K, AU - Perdue,M L, AU - Mo,D, AU - Ji,Y, AU - Woods,L, AU - Hietala,S, AU - Bryant,M, PY - 1999/4/7/pubmed PY - 2000/3/21/medline PY - 1999/4/7/entrez SP - 1132 EP - 8 JF - The Journal of infectious diseases JO - J Infect Dis VL - 179 IS - 5 N2 - Recombinant reassortment technology was used to prepare H5N1 influenza vaccine strains containing a modified hemagglutinin (HA) gene and neuraminidase gene from the A/Hong Kong/156/97 and A/Hong Kong/483/97 isolates and the internal genes from the attenuated cold-adapted A/Ann Arbor/6/60 influenza virus strain. The HA cleavage site (HA1/HA2) of each H5N1 isolate was modified to resemble that of "low-pathogenic" avian strains. Five of 6 basic amino acids at the cleavage site were deleted, and a threonine was added upstream of the remaining arginine. The H5 HA cleavage site modification resulted in the expected trypsin-dependent phenotype without altering the antigenic character of the H5 HA molecule. The temperature-sensitive and cold-adapted phenotype of the attenuated parent virus was maintained in the recombinant strains, and they grew to 108.5-9.4 EID50/mL in eggs. Both H5N1 vaccine virus strains were safe and immunogenic in ferrets and protected chickens against wild-type H5N1 virus challenge. SN - 0022-1899 UR - https://www.unboundmedicine.com/medline/citation/10191214/Recombinant_influenza_A_virus_vaccines_for_the_pathogenic_human_A/Hong_Kong/97__H5N1__viruses_ L2 - https://academic.oup.com/jid/article-lookup/doi/10.1086/314713 DB - PRIME DP - Unbound Medicine ER -