Intranasal administration of a proteosome-influenza vaccine is well-tolerated and induces serum and nasal secretion influenza antibodies in healthy human subjects
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Treanor, J
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机构:Univ Rochester, Sch Med, Infect Dis Unit, Rochester, NY 14642 USA
Treanor, J
Nolan, C
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机构:Univ Rochester, Sch Med, Infect Dis Unit, Rochester, NY 14642 USA
Nolan, C
O'Brien, D
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机构:Univ Rochester, Sch Med, Infect Dis Unit, Rochester, NY 14642 USA
O'Brien, D
Burt, D
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机构:Univ Rochester, Sch Med, Infect Dis Unit, Rochester, NY 14642 USA
Burt, D
Lowell, G
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机构:Univ Rochester, Sch Med, Infect Dis Unit, Rochester, NY 14642 USA
Lowell, G
Linden, J
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机构:Univ Rochester, Sch Med, Infect Dis Unit, Rochester, NY 14642 USA
Linden, J
Fries, L
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机构:Univ Rochester, Sch Med, Infect Dis Unit, Rochester, NY 14642 USA
Fries, L
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[1] Univ Rochester, Sch Med, Infect Dis Unit, Rochester, NY 14642 USA
[2] ID Biomed Quebec, St Laurent, PQ H4S 2A1, Canada
Two randomized, blinded, active comparator-controlled trials of a prototype monovalent A/Beijing/262/95 (H1N1) - proteosome vaccine delivered by intranasal spray were performed in healthy adults. Overall, the intranasal proteosome-adjuvanted vaccine was well-tolerated with only mild stuffy nose and rhinorrhea seen more frequently in recipients of vaccine than in recipients of intranasal saline, and there were no serious adverse events. The intranasal proteosome-adjuvanted vaccine induced serum hernagglutination inhibiting (HAI) and nasal secretory IgA (sIgA) responses specific for the influenza antigen. Serum HAI responses were most influenced by the dosage level, whereas mucosal sIgA responses, although demonstrable with both single-dose and two-dose vaccine regimens, appeared to be greater in response to two-dose regimens (regardless of dose level). Further evaluation of mucosal influenza immunization using the proteosome adjuvant/delivery system is clearly warranted. (c) 2005 Elsevier Ltd. All rights reserved.