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Adenovirus as a carrier for the development of influenza virus-free avian influenza vaccines

Identifieur interne : 000356 ( Ncbi/Merge ); précédent : 000355; suivant : 000357

Adenovirus as a carrier for the development of influenza virus-free avian influenza vaccines

Auteurs : De-Chu C. Tang ; Jianfeng Zhang ; Haroldo Toro ; Zhongkai Shi ; Kent R. Van Kampen

Source :

RBID : PMC:2778197

Abstract

A long-sought goal during the battle against avian influenza is to develop a new generation of vaccines capable of mass immunizing humans as well as poultry (the major source of avian influenza for human infections) in a timely manner. Although administration of the currently licensed influenza vaccine is effective in eliciting protective immunity against seasonal influenza, this approach is associated with a number of insurmountable problems for preventing an avian influenza pandemic. Many of the hurdles may be eliminated by developing new avian influenza vaccines that do not require the propagation of an influenza virus during vaccine production. Replication-competent adenovirus-free adenovirus vectors hold promise as a carrier for influenza virus-free avian influenza vaccines owing to their safety profile and rapid manufacture using cultured suspension cells in a serum-free medium. Simple and efficient mass-immunization protocols, including nasal spray for people and automated in ovo vaccination for poultry, convey another advantage for this class of vaccines. In contrast to parenteral injection of adenovirus vector, the potency of adenovirus-vectored nasal vaccine is not appreciably interfered by pre-existing immunity to adenovirus.


Url:
DOI: 10.1586/erv.09.1
PubMed: 19348562
PubMed Central: 2778197

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PMC:2778197

Le document en format XML

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<name sortKey="Tang, De Chu C" sort="Tang, De Chu C" uniqKey="Tang D" first="De-Chu C" last="Tang">De-Chu C. Tang</name>
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<name sortKey="Zhang, Jianfeng" sort="Zhang, Jianfeng" uniqKey="Zhang J" first="Jianfeng" last="Zhang">Jianfeng Zhang</name>
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<name sortKey="Toro, Haroldo" sort="Toro, Haroldo" uniqKey="Toro H" first="Haroldo" last="Toro">Haroldo Toro</name>
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<name sortKey="Shi, Zhongkai" sort="Shi, Zhongkai" uniqKey="Shi Z" first="Zhongkai" last="Shi">Zhongkai Shi</name>
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<p id="P1">A long-sought goal during the battle against avian influenza is to develop a new generation of vaccines capable of mass immunizing humans as well as poultry (the major source of avian influenza for human infections) in a timely manner. Although administration of the currently licensed influenza vaccine is effective in eliciting protective immunity against seasonal influenza, this approach is associated with a number of insurmountable problems for preventing an avian influenza pandemic. Many of the hurdles may be eliminated by developing new avian influenza vaccines that do not require the propagation of an influenza virus during vaccine production. Replication-competent adenovirus-free adenovirus vectors hold promise as a carrier for influenza virus-free avian influenza vaccines owing to their safety profile and rapid manufacture using cultured suspension cells in a serum-free medium. Simple and efficient mass-immunization protocols, including nasal spray for people and automated
<italic>in ovo</italic>
vaccination for poultry, convey another advantage for this class of vaccines. In contrast to parenteral injection of adenovirus vector, the potency of adenovirus-vectored nasal vaccine is not appreciably interfered by pre-existing immunity to adenovirus.</p>
</div>
</front>
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<pmc-comment>The publisher of this article does not allow downloading of the full text in XML form.</pmc-comment>
<pmc-dir>properties manuscript</pmc-dir>
<front>
<journal-meta>
<journal-id journal-id-type="nlm-journal-id">101155475</journal-id>
<journal-id journal-id-type="pubmed-jr-id">30416</journal-id>
<journal-id journal-id-type="nlm-ta">Expert Rev Vaccines</journal-id>
<journal-title>Expert review of vaccines</journal-title>
<issn pub-type="ppub">1476-0584</issn>
<issn pub-type="epub">1744-8395</issn>
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<article-id pub-id-type="pmid">19348562</article-id>
<article-id pub-id-type="pmc">2778197</article-id>
<article-id pub-id-type="doi">10.1586/erv.09.1</article-id>
<article-id pub-id-type="manuscript">NIHMS117538</article-id>
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<subj-group subj-group-type="heading">
<subject>Article</subject>
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<title-group>
<article-title>Adenovirus as a carrier for the development of influenza virus-free avian influenza vaccines</article-title>
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<contrib contrib-type="author">
<name>
<surname>Tang</surname>
<given-names>De-chu C</given-names>
</name>
<degrees>PhD</degrees>
<role>Founder</role>
<xref ref-type="corresp" rid="cor1"></xref>
<aff id="A1">Vice President of Research, and Chief Technical Officer, Vaxin Inc., 1500 First Avenue North, Birmingham, AL 35203, USA, Tel.: +1 205 909 3738, Fax: +1 205 307 6503,
<email>tang@vaxin.com</email>
</aff>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Zhang</surname>
<given-names>Jianfeng</given-names>
</name>
<degrees>PhD</degrees>
<role>Scientist</role>
<aff id="A2">Vaxin Inc., 1500 First Avenue North, Birmingham, AL 35203, USA, Tel.: +1 205 909 3740, Fax: +1 205 307 6503,
<email>zhang@vaxin.com</email>
</aff>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Toro</surname>
<given-names>Haroldo</given-names>
</name>
<degrees>DVM, PhD</degrees>
<role>Professor</role>
<aff id="A3">Department of Pathobiology, Auburn University, 264 Greene Hall, Auburn, AL 36849, USA, Tel.: +1 334 844 2662, Fax: +1 334 844 2652,
<email>torohar@vetmed.auburn.edu</email>
</aff>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Shi</surname>
<given-names>Zhongkai</given-names>
</name>
<degrees>MD</degrees>
<role>Scientist</role>
<aff id="A4">Vaxin Inc., 1500 First Avenue North, Birmingham, AL 35203, USA, Tel.: +1 205 909 3751, Fax: +1 205 307 6503,
<email>shi@vaxin.com</email>
</aff>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Van Kampen</surname>
<given-names>Kent R</given-names>
</name>
<degrees>DVM, PhD</degrees>
<role>Chief Operating Officer</role>
<aff id="A5">Vaxin Inc., 1500 First Avenue North, Birmingham, AL 35203, USA, Tel.: +1 205 909 3737, Fax: +1 205 307 6503,
<email>vankampen@vaxin.com</email>
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</contrib>
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<author-notes>
<corresp id="cor1">
<label></label>
Author for correspondence, Vaxin Inc., 1500 First Avenue North, Birmingham, AL 35203, USA, Tel.: +1 205 909 3738, Fax: +1 205 307 6503,
<email>tang@vaxin.com</email>
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<pub-date pub-type="nihms-submitted">
<day>18</day>
<month>5</month>
<year>2009</year>
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<pub-date pub-type="ppub">
<month>4</month>
<year>2009</year>
</pub-date>
<pub-date pub-type="pmc-release">
<day>1</day>
<month>2</month>
<year>2010</year>
</pub-date>
<volume>8</volume>
<issue>4</issue>
<fpage>469</fpage>
<lpage>481</lpage>
<permissions>
<copyright-statement>© 2009 Expert Reviews Ltd</copyright-statement>
<copyright-year>2009</copyright-year>
</permissions>
<abstract>
<p id="P1">A long-sought goal during the battle against avian influenza is to develop a new generation of vaccines capable of mass immunizing humans as well as poultry (the major source of avian influenza for human infections) in a timely manner. Although administration of the currently licensed influenza vaccine is effective in eliciting protective immunity against seasonal influenza, this approach is associated with a number of insurmountable problems for preventing an avian influenza pandemic. Many of the hurdles may be eliminated by developing new avian influenza vaccines that do not require the propagation of an influenza virus during vaccine production. Replication-competent adenovirus-free adenovirus vectors hold promise as a carrier for influenza virus-free avian influenza vaccines owing to their safety profile and rapid manufacture using cultured suspension cells in a serum-free medium. Simple and efficient mass-immunization protocols, including nasal spray for people and automated
<italic>in ovo</italic>
vaccination for poultry, convey another advantage for this class of vaccines. In contrast to parenteral injection of adenovirus vector, the potency of adenovirus-vectored nasal vaccine is not appreciably interfered by pre-existing immunity to adenovirus.</p>
</abstract>
<kwd-group>
<kwd>adenovirus</kwd>
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<contract-num rid="AI1">R44 AI068285-02 ||AI</contract-num>
<contract-num rid="AI1">R43 AI068285-01 ||AI</contract-num>
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