Citation
Desheva, J A., et al. "Characterization of an Influenza a H5N2 Reassortant as a Candidate for Live-attenuated and Inactivated Vaccines Against Highly Pathogenic H5N1 Viruses With Pandemic Potential." Vaccine, vol. 24, no. 47-48, 2006, pp. 6859-66.
Desheva JA, Lu XH, Rekstin AR, et al. Characterization of an influenza A H5N2 reassortant as a candidate for live-attenuated and inactivated vaccines against highly pathogenic H5N1 viruses with pandemic potential. Vaccine. 2006;24(47-48):6859-66.
Desheva, J. A., Lu, X. H., Rekstin, A. R., Rudenko, L. G., Swayne, D. E., Cox, N. J., Katz, J. M., & Klimov, A. I. (2006). Characterization of an influenza A H5N2 reassortant as a candidate for live-attenuated and inactivated vaccines against highly pathogenic H5N1 viruses with pandemic potential. Vaccine, 24(47-48), 6859-66.
Desheva JA, et al. Characterization of an Influenza a H5N2 Reassortant as a Candidate for Live-attenuated and Inactivated Vaccines Against Highly Pathogenic H5N1 Viruses With Pandemic Potential. Vaccine. 2006 Nov 17;24(47-48):6859-66. PubMed PMID: 17050041.
TY - JOUR
T1 - Characterization of an influenza A H5N2 reassortant as a candidate for live-attenuated and inactivated vaccines against highly pathogenic H5N1 viruses with pandemic potential.
AU - Desheva,J A,
AU - Lu,X H,
AU - Rekstin,A R,
AU - Rudenko,L G,
AU - Swayne,D E,
AU - Cox,N J,
AU - Katz,J M,
AU - Klimov,A I,
Y1 - 2006/06/28/
PY - 2006/04/02/received
PY - 2006/05/31/revised
PY - 2006/06/14/accepted
PY - 2006/10/20/pubmed
PY - 2007/1/5/medline
PY - 2006/10/20/entrez
SP - 6859
EP - 66
JF - Vaccine
JO - Vaccine
VL - 24
IS - 47-48
N2 - We generated a high-growth 7:1 reassortant (Len17/H5) that contained the hemagglutinin (HA) gene from non-pathogenic A/Duck/Potsdam/1402-6/86 (H5N2) virus and other genes from the cold-adapted (ca) attenuated A/Leningrad/134/17/57 (H2H2) strain. Len17/H5 demonstrated an attenuated phenotype in mice and did not infect chickens. Mice administered Len17/H5 either as a live-attenuated intranasal vaccine or as an inactivated intramuscular vaccine were substantially protected from lethal challenge with highly pathogenic A/Hong Kong/483/97 (H5N1) virus and were protected from pulmonary infection with antigenically distinct A/Hong Kong/213/2003 (H5N1) virus. The cross-protective effect correlated with the levels of virus-specific mucosal IgA and/or serum IgG antibodies. Our results suggest a new strategy of using classical genetic reassortment between a high-growth ca H2N2 strain and antigenically related non-pathogenic avian viruses to prepare live-attenuated and inactivated vaccines for influenza pandemic.
SN - 0264-410X
UR - https://www.unboundmedicine.com/medline/citation/17050041/Characterization_of_an_influenza_A_H5N2_reassortant_as_a_candidate_for_live_attenuated_and_inactivated_vaccines_against_highly_pathogenic_H5N1_viruses_with_pandemic_potential_
L2 - https://linkinghub.elsevier.com/retrieve/pii/S0264-410X(06)00742-0
DB - PRIME
DP - Unbound Medicine
ER -