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Science 10 August 2007:
Vol. 317. no. 5839, pp. 825 - 828
DOI: 10.1126/science.1135165

Reports

Immunization by Avian H5 Influenza Hemagglutinin Mutants with Altered Receptor Binding Specificity

Zhi-Yong Yang,1* Chih-Jen Wei,1* Wing-Pui Kong,1 Lan Wu,1 Ling Xu,1 David F. Smith,2 Gary J. Nabel1{dagger}

Influenza virus entry is mediated by the receptor binding domain (RBD) of its spike, the hemagglutinin (HA). Adaptation of avian viruses to humans is associated with HA specificity for {alpha}2,6- rather than {alpha}2,3-linked sialic acid (SA) receptors. Here, we define mutations in influenza A subtype H5N1 (avian) HA that alter its specificity for SA either by decreasing {alpha}2,3- or increasing {alpha}2,6-SA recognition. RBD mutants were used to develop vaccines and monoclonal antibodies that neutralized new variants. Structure-based modification of HA specificity can guide the development of preemptive vaccines and therapeutic monoclonal antibodies that can be evaluated before the emergence of human-adapted H5N1 strains.

1 Vaccine Research Center, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health, Building 40, Room 4502, Mailstop Code MSC-3005, 40 Convent Drive, Bethesda, MD 20892, USA.
2 Emory University School of Medicine, 1510 Clifton Road NE, Room 4035, Atlanta, GA 30322, USA.

* These authors contributed equally to this work.

{dagger} To whom correspondence should be addressed. E-mail: gnabel{at}nih.gov

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