The Analysis of B-Cell Epitopes of Influenza Virus Hemagglutinin
Identifieur interne : 000403 ( Main/Exploration ); précédent : 000402; suivant : 000404The Analysis of B-Cell Epitopes of Influenza Virus Hemagglutinin
Auteurs : D. N. Shcherbinin ; S. V. Alekseeva ; M. M. Shmarov ; Yu. A. Smirnov ; B. S. Naroditskiy ; A. L. GintsburgSource :
- Acta Naturae [ 2075-8251 ] ; 2016.
Abstract
Vaccination has been successfully used to prevent influenza for a long time. Influenza virus hemagglutinin (HA), which induces a humoral immune response in humans and protection against the flu, is the main antigenic component of modern influenza vaccines. However, new seasonal and pandemic influenza virus variants with altered structures of HA occasionally occur. This allows the pathogen to avoid neutralization with antibodies produced in response to previous vaccination. Development of a vaccine with the new variants of HA acting as antigens takes a long time. Therefore, during an epidemic, it is important to have passive immunization agents to prevent and treat influenza, which can be monoclonal or single-domain antibodies with universal specificity (broad-spectrum agents). We considered antibodies to conserved epitopes of influenza virus antigens as universal ones. In this paper, we tried to characterize the main B-cell epitopes of hemagglutinin and analyze our own and literature data on broadly neutralizing antibodies. We conducted a computer analysis of the best known conformational epitopes of influenza virus HAs using materials of different databases. The analysis showed that the core of the HA molecule, whose antibodies demonstrate pronounced heterosubtypic activity, can be used as a target for the search for and development of broad-spectrum antibodies to the influenza virus.
Url:
PubMed: 27099781
PubMed Central: 4837568
Affiliations:
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N." last="Shcherbinin">D. N. Shcherbinin</name><affiliation><nlm:aff id="AF1">Federal State Budgetary Institution “Federal Research Centre for Epidemiology and Microbiology named after the honorary academician N.F. Gamaleya” of the Ministry of Health of the Russian Federation, Gamaleya str. 18, Moscow, Russian Federation, 123098</nlm:aff><wicri:noCountry code="subfield">123098</wicri:noCountry></affiliation></author><author><name sortKey="Alekseeva, S V" sort="Alekseeva, S V" uniqKey="Alekseeva S" first="S. V." last="Alekseeva">S. V. Alekseeva</name><affiliation><nlm:aff id="AF1">Federal State Budgetary Institution “Federal Research Centre for Epidemiology and Microbiology named after the honorary academician N.F. Gamaleya” of the Ministry of Health of the Russian Federation, Gamaleya str. 18, Moscow, Russian Federation, 123098</nlm:aff><wicri:noCountry code="subfield">123098</wicri:noCountry></affiliation></author><author><name sortKey="Shmarov, M M" sort="Shmarov, M M" uniqKey="Shmarov M" first="M. M." last="Shmarov">M. M. Shmarov</name><affiliation><nlm:aff id="AF1">Federal State Budgetary Institution “Federal Research Centre for Epidemiology and Microbiology named after the honorary academician N.F. Gamaleya” of the Ministry of Health of the Russian Federation, Gamaleya str. 18, Moscow, Russian Federation, 123098</nlm:aff><wicri:noCountry code="subfield">123098</wicri:noCountry></affiliation></author><author><name sortKey="Smirnov, Yu A" sort="Smirnov, Yu A" uniqKey="Smirnov Y" first="Yu. A." last="Smirnov">Yu. A. Smirnov</name><affiliation><nlm:aff id="AF1">Federal State Budgetary Institution “Federal Research Centre for Epidemiology and Microbiology named after the honorary academician N.F. Gamaleya” of the Ministry of Health of the Russian Federation, Gamaleya str. 18, Moscow, Russian Federation, 123098</nlm:aff><wicri:noCountry code="subfield">123098</wicri:noCountry></affiliation></author><author><name sortKey="Naroditskiy, B S" sort="Naroditskiy, B S" uniqKey="Naroditskiy B" first="B. S." last="Naroditskiy">B. S. Naroditskiy</name><affiliation><nlm:aff id="AF1">Federal State Budgetary Institution “Federal Research Centre for Epidemiology and Microbiology named after the honorary academician N.F. Gamaleya” of the Ministry of Health of the Russian Federation, Gamaleya str. 18, Moscow, Russian Federation, 123098</nlm:aff><wicri:noCountry code="subfield">123098</wicri:noCountry></affiliation></author><author><name sortKey="Gintsburg, A L" sort="Gintsburg, A L" uniqKey="Gintsburg A" first="A. L." last="Gintsburg">A. L. Gintsburg</name><affiliation><nlm:aff id="AF1">Federal State Budgetary Institution “Federal Research Centre for Epidemiology and Microbiology named after the honorary academician N.F. Gamaleya” of the Ministry of Health of the Russian Federation, Gamaleya str. 18, Moscow, Russian Federation, 123098</nlm:aff><wicri:noCountry code="subfield">123098</wicri:noCountry></affiliation></author></analytic><series><title level="j">Acta Naturae</title><idno type="ISSN">2075-8251</idno><imprint><date when="2016">2016</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>Vaccination has been successfully used to prevent influenza for a long time.
Influenza virus hemagglutinin (HA), which induces a humoral immune response in
humans and protection against the flu, is the main antigenic component of
modern influenza vaccines. However, new seasonal and pandemic influenza virus
variants with altered structures of HA occasionally occur. This allows the
pathogen to avoid neutralization with antibodies produced in response to
previous vaccination. Development of a vaccine with the new variants of HA
acting as antigens takes a long time. Therefore, during an epidemic, it is
important to have passive immunization agents to prevent and treat influenza,
which can be monoclonal or single-domain antibodies with universal specificity
(broad-spectrum agents). We considered antibodies to conserved epitopes of
influenza virus antigens as universal ones. In this paper, we tried to
characterize the main B-cell epitopes of hemagglutinin and analyze our own and
literature data on broadly neutralizing antibodies. We conducted a computer
analysis of the best known conformational epitopes of influenza virus HAs using
materials of different databases. The analysis showed that the core of the HA
molecule, whose antibodies demonstrate pronounced heterosubtypic activity, can
be used as a target for the search for and development of broad-spectrum
antibodies to the influenza virus.
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Gintsburg</name><name sortKey="Naroditskiy, B S" sort="Naroditskiy, B S" uniqKey="Naroditskiy B" first="B. S." last="Naroditskiy">B. S. Naroditskiy</name><name sortKey="Shcherbinin, D N" sort="Shcherbinin, D N" uniqKey="Shcherbinin D" first="D. N." last="Shcherbinin">D. N. Shcherbinin</name><name sortKey="Shmarov, M M" sort="Shmarov, M M" uniqKey="Shmarov M" first="M. M." last="Shmarov">M. M. Shmarov</name><name sortKey="Smirnov, Yu A" sort="Smirnov, Yu A" uniqKey="Smirnov Y" first="Yu. A." last="Smirnov">Yu. A. Smirnov</name></noCountry></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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