Progress and Challenges toward the Development of Vaccines against Avian Infectious Bronchitis
Identifieur interne : 000534 ( Pmc/Checkpoint ); précédent : 000533; suivant : 000535Progress and Challenges toward the Development of Vaccines against Avian Infectious Bronchitis
Auteurs : Faruku Bande [Malaisie, Nigeria] ; Siti Suri Arshad [Malaisie] ; Mohd Hair Bejo [Malaisie] ; Hassan Moeini [Allemagne] ; Abdul Rahman Omar [Malaisie]Source :
- Journal of Immunology Research [ 2314-8861 ] ; 2015.
Abstract
Avian infectious bronchitis (IB) is a widely distributed poultry disease that has huge economic impact on poultry industry. The continuous emergence of new IBV genotypes and lack of cross protection among different IBV genotypes have been an important challenge. Although live attenuated IB vaccines remarkably induce potent immune response, the potential risk of reversion to virulence, neutralization by the maternal antibodies, and recombination and mutation events are important concern on their usage. On the other hand, inactivated vaccines induce a weaker immune response and may require multiple dosing and/or the use of adjuvants that probably have potential safety risks and increased economic burdens. Consequently, alternative IB vaccines are widely sought. Recent advances in recombinant DNA technology have resulted in experimental IB vaccines that show promise in antibody and T-cells responses, comparable to live attenuated vaccines. Recombinant DNA vaccines have also been enhanced to target multiple serotypes and their efficacy has been improved using delivery vectors, nanoadjuvants, and
Url:
DOI: 10.1155/2015/424860
PubMed: 25954763
PubMed Central: 4411447
Affiliations:
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PMC:4411447Le document en format XML
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<front><div type="abstract" xml:lang="en"><p>Avian infectious bronchitis (IB) is a widely distributed poultry disease that has huge economic impact on poultry industry. The continuous emergence of new IBV genotypes and lack of cross protection among different IBV genotypes have been an important challenge. Although live attenuated IB vaccines remarkably induce potent immune response, the potential risk of reversion to virulence, neutralization by the maternal antibodies, and recombination and mutation events are important concern on their usage. On the other hand, inactivated vaccines induce a weaker immune response and may require multiple dosing and/or the use of adjuvants that probably have potential safety risks and increased economic burdens. Consequently, alternative IB vaccines are widely sought. Recent advances in recombinant DNA technology have resulted in experimental IB vaccines that show promise in antibody and T-cells responses, comparable to live attenuated vaccines. Recombinant DNA vaccines have also been enhanced to target multiple serotypes and their efficacy has been improved using delivery vectors, nanoadjuvants, and <italic>in ovo</italic>
vaccination approaches. Although most recombinant IB DNA vaccines are yet to be licensed, it is expected that these types of vaccines may hold sway as future vaccines for inducing a cross protection against multiple IBV serotypes.</p>
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<pmc article-type="research-article"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">J Immunol Res</journal-id>
<journal-id journal-id-type="iso-abbrev">J Immunol Res</journal-id>
<journal-id journal-id-type="publisher-id">JIR</journal-id>
<journal-title-group><journal-title>Journal of Immunology Research</journal-title>
</journal-title-group>
<issn pub-type="ppub">2314-8861</issn>
<issn pub-type="epub">2314-7156</issn>
<publisher><publisher-name>Hindawi Publishing Corporation</publisher-name>
</publisher>
</journal-meta>
<article-meta><article-id pub-id-type="pmid">25954763</article-id>
<article-id pub-id-type="pmc">4411447</article-id>
<article-id pub-id-type="doi">10.1155/2015/424860</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Review Article</subject>
</subj-group>
</article-categories>
<title-group><article-title>Progress and Challenges toward the Development of Vaccines against Avian Infectious Bronchitis</article-title>
</title-group>
<contrib-group><contrib contrib-type="author"><name><surname>Bande</surname>
<given-names>Faruku</given-names>
</name>
<xref ref-type="aff" rid="I1"><sup>1</sup>
</xref>
<xref ref-type="aff" rid="I2"><sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Arshad</surname>
<given-names>Siti Suri</given-names>
</name>
<xref ref-type="aff" rid="I1"><sup>1</sup>
</xref>
<xref ref-type="corresp" rid="cor1"><sup>*</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Hair Bejo</surname>
<given-names>Mohd</given-names>
</name>
<xref ref-type="aff" rid="I1"><sup>1</sup>
</xref>
<xref ref-type="aff" rid="I3"><sup>3</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Moeini</surname>
<given-names>Hassan</given-names>
</name>
<xref ref-type="aff" rid="I4"><sup>4</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Omar</surname>
<given-names>Abdul Rahman</given-names>
</name>
<xref ref-type="aff" rid="I1"><sup>1</sup>
</xref>
</contrib>
</contrib-group>
<aff id="I1"><sup>1</sup>
Department of Veterinary Pathology and Microbiology, Faculty of Veterinary Medicine, Universiti Putra Malaysia (UPM), 43400 Serdang, Selangor, Malaysia</aff>
<aff id="I2"><sup>2</sup>
Department of Veterinary Services, Ministry of Animal Health and Fisheries Development, PMB 2109, Usman Faruk Secretariat, Sokoto 840221, Sokoto State, Nigeria</aff>
<aff id="I3"><sup>3</sup>
Laboratory of Vaccine and Immunotherapeutics, Institute of Bioscience, Universiti Putra Malaysia (UPM), 43400 Serdang, Selangor, Malaysia</aff>
<aff id="I4"><sup>4</sup>
Department of Virus-Associated Tumours (F100), German Cancer Research Centre, Im Neuenheimer Feld 242, 69120 Heidelberg, Germany</aff>
<author-notes><corresp id="cor1">*Siti Suri Arshad: <email>suri@upm.edu.my</email>
</corresp>
<fn fn-type="other"><p>Academic Editor: Peirong Jiao</p>
</fn>
</author-notes>
<pub-date pub-type="ppub"><year>2015</year>
</pub-date>
<pub-date pub-type="epub"><day>14</day>
<month>4</month>
<year>2015</year>
</pub-date>
<volume>2015</volume>
<elocation-id>424860</elocation-id>
<history><date date-type="received"><day>27</day>
<month>12</month>
<year>2014</year>
</date>
<date date-type="rev-recd"><day>20</day>
<month>3</month>
<year>2015</year>
</date>
<date date-type="accepted"><day>23</day>
<month>3</month>
<year>2015</year>
</date>
</history>
<permissions><copyright-statement>Copyright © 2015 Faruku Bande et al.</copyright-statement>
<copyright-year>2015</copyright-year>
<license xlink:href="https://creativecommons.org/licenses/by/3.0/"><license-p>This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
</license>
</permissions>
<abstract><p>Avian infectious bronchitis (IB) is a widely distributed poultry disease that has huge economic impact on poultry industry. The continuous emergence of new IBV genotypes and lack of cross protection among different IBV genotypes have been an important challenge. Although live attenuated IB vaccines remarkably induce potent immune response, the potential risk of reversion to virulence, neutralization by the maternal antibodies, and recombination and mutation events are important concern on their usage. On the other hand, inactivated vaccines induce a weaker immune response and may require multiple dosing and/or the use of adjuvants that probably have potential safety risks and increased economic burdens. Consequently, alternative IB vaccines are widely sought. Recent advances in recombinant DNA technology have resulted in experimental IB vaccines that show promise in antibody and T-cells responses, comparable to live attenuated vaccines. Recombinant DNA vaccines have also been enhanced to target multiple serotypes and their efficacy has been improved using delivery vectors, nanoadjuvants, and <italic>in ovo</italic>
vaccination approaches. Although most recombinant IB DNA vaccines are yet to be licensed, it is expected that these types of vaccines may hold sway as future vaccines for inducing a cross protection against multiple IBV serotypes.</p>
</abstract>
</article-meta>
</front>
<floats-group><fig id="fig1" orientation="portrait" position="float"><label>Figure 1</label>
<caption><p><italic>Predicted 3-dimensional structure of S1-glycoprotein (a) and nucleocapsid protein (b), determinants of Massachusetts strain of avian infectious bronchitis virus.</italic>
Structures are drawn using SWISS homology modeller available online at <ext-link ext-link-type="uri" xlink:href="http://swissmodel.expasy.org/">http://swissmodel.expasy.org/</ext-link>
.</p>
</caption>
<graphic xlink:href="JIR2015-424860.001"></graphic>
</fig>
<fig id="fig2" orientation="portrait" position="float"><label>Figure 2</label>
<caption><p><italic>Neighbour-joining phylogenetics showing relationship in S1-glycoprotein of classical (pink) and variant (blue) IBV strains.</italic>
The tree reliability was assessed using 1000-bootstrap confidence and branching pattern is supported by 91.7–100% bootstraps values and associated taxa show 82% pairwise identity. Phylogenetic analysis was carried out using Geneious software version R8.</p>
</caption>
<graphic xlink:href="JIR2015-424860.002"></graphic>
</fig>
<fig id="fig3" orientation="portrait" position="float"><label>Figure 3</label>
<caption><p>Summary of major IB vaccines and important limitations associated with the vaccine types.</p>
</caption>
<graphic xlink:href="JIR2015-424860.003"></graphic>
</fig>
</floats-group>
</pmc>
<affiliations><list><country><li>Allemagne</li>
<li>Malaisie</li>
<li>Nigeria</li>
</country>
<region><li>Bade-Wurtemberg</li>
<li>District de Karlsruhe</li>
</region>
<settlement><li>Heidelberg</li>
</settlement>
</list>
<tree><country name="Malaisie"><noRegion><name sortKey="Bande, Faruku" sort="Bande, Faruku" uniqKey="Bande F" first="Faruku" last="Bande">Faruku Bande</name>
</noRegion>
<name sortKey="Arshad, Siti Suri" sort="Arshad, Siti Suri" uniqKey="Arshad S" first="Siti Suri" last="Arshad">Siti Suri Arshad</name>
<name sortKey="Hair Bejo, Mohd" sort="Hair Bejo, Mohd" uniqKey="Hair Bejo M" first="Mohd" last="Hair Bejo">Mohd Hair Bejo</name>
<name sortKey="Hair Bejo, Mohd" sort="Hair Bejo, Mohd" uniqKey="Hair Bejo M" first="Mohd" last="Hair Bejo">Mohd Hair Bejo</name>
<name sortKey="Omar, Abdul Rahman" sort="Omar, Abdul Rahman" uniqKey="Omar A" first="Abdul Rahman" last="Omar">Abdul Rahman Omar</name>
</country>
<country name="Nigeria"><noRegion><name sortKey="Bande, Faruku" sort="Bande, Faruku" uniqKey="Bande F" first="Faruku" last="Bande">Faruku Bande</name>
</noRegion>
</country>
<country name="Allemagne"><region name="Bade-Wurtemberg"><name sortKey="Moeini, Hassan" sort="Moeini, Hassan" uniqKey="Moeini H" first="Hassan" last="Moeini">Hassan Moeini</name>
</region>
</country>
</tree>
</affiliations>
</record>
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