New Pre-pandemic Influenza Vaccines: An Egg-and Adjuvant-independent Human Adenoviral Vector Strategy Induces Long-lasting Protective Immune Responses in Mice
Identifieur interne : 000669 ( Pmc/Checkpoint ); précédent : 000668; suivant : 000670New Pre-pandemic Influenza Vaccines: An Egg-and Adjuvant-independent Human Adenoviral Vector Strategy Induces Long-lasting Protective Immune Responses in Mice
Auteurs : Ma Hoelscher [Géorgie (pays)] ; L. Jayashankar [États-Unis] ; S. Garg [Géorgie (pays)] ; V. Veguilla [Géorgie (pays)] ; N. Singh [États-Unis] ; Jm Katz [Géorgie (pays)] ; Sk Mittal [États-Unis] ; S. Sambhara [Géorgie (pays)]Source :
- Clinical pharmacology and therapeutics [ 0009-9236 ] ; 2007.
Abstract
Highly pathogenic avian H5N1 influenza viruses that are currently circulating in southeast Asia may acquire the potential to cause the next influenza pandemic. A number of alternate approaches are being pursued to generate cross-protective, dose-sparing, safe, and effective vaccines, as traditional vaccine approaches, i.e., embryonated egg-grown, are not immunogenic. We developed a replication-incompetent adenoviral vector-based, adjuvant-and egg-independent pandemic influenza vaccine strategy as a potential alternative to conventional egg-derived vaccines. In this paper, we address suboptimal dose and longevity of vaccine-induced protective immunity and demonstrate that a vaccine dose as little as 1 × 106 plaque-forming unit (PFU) is sufficient to induce protective immune responses against a highly pathogenic H5N1 virus. Furthermore, the vaccine-induced humoral and cellular immune responses and protective immunity persisted at least for a year.
Url:
DOI: 10.1038/sj.clpt.6100418
PubMed: 17957181
PubMed Central: 2793094
Affiliations:
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<front><div type="abstract" xml:lang="en"><p id="P2">Highly pathogenic avian H5N1 influenza viruses that are currently circulating in southeast Asia may acquire the potential to cause the next influenza pandemic. A number of alternate approaches are being pursued to generate cross-protective, dose-sparing, safe, and effective vaccines, as traditional vaccine approaches, i.e., embryonated egg-grown, are not immunogenic. We developed a replication-incompetent adenoviral vector-based, adjuvant-and egg-independent pandemic influenza vaccine strategy as a potential alternative to conventional egg-derived vaccines. In this paper, we address suboptimal dose and longevity of vaccine-induced protective immunity and demonstrate that a vaccine dose as little as 1 × 10<sup>6</sup>
plaque-forming unit (PFU) is sufficient to induce protective immune responses against a highly pathogenic H5N1 virus. Furthermore, the vaccine-induced humoral and cellular immune responses and protective immunity persisted at least for a year.</p>
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<aff id="A1"><label>1</label>
Influenza Division, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia</aff>
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Department of Comparative Pathobiology, School of Veterinary Medicine, Purdue University, West Lafayette, Indiana</aff>
<author-notes><corresp id="cor1">Correspondence: S Sambhara (<email>ssambhara@cdc.gov</email>
) or SK Mittal (<email>mittal@purdue.edu</email>
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<fn id="FN1" fn-type="equal"><label>3</label>
<p id="P1">These authors contributed equally to this work.</p>
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<fn id="FN3" fn-type="conflict"><p id="P21"><bold>CONFLICT OF INTEREST</bold>
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<p id="P22">The authors declared no conflict of interest.</p>
</fn>
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<abstract><p id="P2">Highly pathogenic avian H5N1 influenza viruses that are currently circulating in southeast Asia may acquire the potential to cause the next influenza pandemic. A number of alternate approaches are being pursued to generate cross-protective, dose-sparing, safe, and effective vaccines, as traditional vaccine approaches, i.e., embryonated egg-grown, are not immunogenic. We developed a replication-incompetent adenoviral vector-based, adjuvant-and egg-independent pandemic influenza vaccine strategy as a potential alternative to conventional egg-derived vaccines. In this paper, we address suboptimal dose and longevity of vaccine-induced protective immunity and demonstrate that a vaccine dose as little as 1 × 10<sup>6</sup>
plaque-forming unit (PFU) is sufficient to induce protective immune responses against a highly pathogenic H5N1 virus. Furthermore, the vaccine-induced humoral and cellular immune responses and protective immunity persisted at least for a year.</p>
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