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The Interaction of Influenza Virus Haemagglutinin with Phospholipid Vesicles — Morphological and Immunological Studies

¹ Division of Virology, National Institute for Biological Standards and Control, Holly Hill, Hampstead, London NW3 6RB
² Chester Beatty Research Institute, Fulham Road, London SW3
³ Clinical Research Centre, Northwick Park Hospital, Watford Road, Harrow, Middlesex, U.K.

HA—lipid spheres or ‘virosomes’ were prepared using neutral or negatively charged, but not positively charged, phospholipids. Virosomes were similar in size and shape to native virus particles although the HA subunits were at least twofold less numerous on the virosomes. The HA subunits were attached by their narrow end to the lipid bilayer, and could be removed by digestion with bromelain. However, HA subunits released from intact virus by digestion with bromelain, which removed the hydrophobic tail of the molecule, could not attach to liposomes. Measurements of HA spikes before (mean length 14.2 ± 0.9 nm) and after attachment to liposomes (mean length 13.3 ± 0.7 nm) and examination of freeze-fractured virosomes indicated that the HA did not penetrate deeply into the lipid bilayer. Similarly, HA subunits did not penetrate deeply into the lipid of virus particles. NP and M proteins could be attached to liposomes but could not be visualized by electron microscopy. Virosomes were taken up by Vero cells by viropexis with no evidence of fusion. Incorporation of HA or NP on to virosomes resulted in increased immunogenicity compared to free HA subunits or NP respectively. This adjuvant activity was not apparent in simple mixtures of HA and liposomes. The antibody induced by HA subunits, virions and virosomes reacted similarly with strain-specific (SS) antigenic determinants of the haemagglutinin.

Received 18 July 1980; accepted 22 September 1980.