Baculovirus-derived hemagglutinin vaccines protect against lethal influenza infections by avian H5 and H7 subtypes

Baculoviruses were engineered to express hemagglutinin (HA) genes of recent avian influenza (AI) isolates of the H5 and H7 subtypes, The proteins were expressed as either intact (H7) or slightly truncated versions (H5). In bo th cases purified H4 proteins from insect cell cultures retained hemaggluti nation activity and formed rosettes in solution, indicating proper folding. Although immunogenic in this form, these proteins were more effective when administered subcutaneously in a water-in-oil emulsion. One or two-day-old specific pathogen free (SPF) White Rock chickens, free of maternal AI anti bodies, responded with variable serum Hi titers. but in some cases the tite rs were comparable to those achieved using whole virus preparations. Vaccin ation of three-week-old chickens with 1.0 mu g of protein per bird generate d a more consistent serum antibody response with an average geometric mean titer (GMT) of 121 (H5) and 293 (H7) at 21 days postvaccination. When chall enged with highly pathogenic strains of the corresponding AI subtypes, the vaccinated birds were completely protected against lethal infection and in some cases exhibited reduced or no cloacal shedding at 3 days postinfection . Vaccine protocols employing these recombinant HA proteins will not elicit an immune response against internal AI proteins and thus will not interfer e with epidemiological surveys of natural influenza infections in the field . (C) 1999 Elsevier Science Ltd. All rights reserved.