In vitro Antiviral Activity of Recombinant Antibodies of IgG and IgA Isotypes to Hemagglutinin of the Influenza A Virus
- 作者: Argentova V.V.1, Aliev T.K.2, Zarubaev V.V.3, Klotchenko S.A.3, Shtro A.A.3, Sergeeva M.V.3, Toporova V.A.4, Dolgikh D.A.1,4, Sveshnikov P.G.5, Vasin V.A.3, Kirpichnikov M.P.1,4
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隶属关系:
- Department of Bioengineering, Faculty of Biology
- Department of Chemical Enzymology, Faculty of Chemistry
- Research Institute of Influenza
- Shemyakin–Ovchinnikov Institute of Bioorganic Chemistry
- Russian Research Center for Molecular Diagnostics and Therapy
- 期: 卷 51, 编号 6 (2017)
- 页面: 804-812
- 栏目: Current Trends in the Application of Monoclonal Antibodies Special Issue
- URL: https://journals.rcsi.science/0026-8933/article/view/163293
- DOI: https://doi.org/10.1134/S0026893317060024
- ID: 163293
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详细
Seasonal and highly infectious strains of the influenza A and influenza B viruses cause millions of cases of severe complications in elderly people, children, and patients with immune diseases each year. Immunoglobulin A (IgA), which is an active component of humoral immunity, can prevent the spread of the virus in the upper respiratory tract. The preparation and study of the properties of recombinant virus-specific IgA could be an important approach to finding new means of preventing and treating influenza. Based on CHO DG44 cells, we developed stable monoclonal cell lines that produce monomeric and dimeric antibodies FI6-IgA1 and FI6-IgA2m1 to hemagglutinin (HA) of the influenza A virus. When studying the productivity, growth, and stability of the obtained clones, we found that the dimeric form of antibodies of IgA1 isotype is superior to other forms. The dimeric form of IgA antibodies plays a key role in mucosal immunity. Recognizing the prospects of using dimeric IgA as prophylactic and therapeutic mucosal drugs for viral infections, we studied their virus-neutralizing and antiviral activities on MDCK cell culture and compared them with the antibodies of the IgG1 isotype. This study presents the data on antiviral and virus-neutralizing activities of the FI6-IgA1 dimers to seasonal and highly infectious strains of influenza A virus.
作者简介
V. Argentova
Department of Bioengineering, Faculty of Biology
编辑信件的主要联系方式.
Email: vicarg@rambler.ru
俄罗斯联邦, Moscow, 119234
T. Aliev
Department of Chemical Enzymology, Faculty of Chemistry
Email: vicarg@rambler.ru
俄罗斯联邦, Moscow, 119991
V. Zarubaev
Research Institute of Influenza
Email: vicarg@rambler.ru
俄罗斯联邦, St. Petersburg, 197376
S. Klotchenko
Research Institute of Influenza
Email: vicarg@rambler.ru
俄罗斯联邦, St. Petersburg, 197376
A. Shtro
Research Institute of Influenza
Email: vicarg@rambler.ru
俄罗斯联邦, St. Petersburg, 197376
M. Sergeeva
Research Institute of Influenza
Email: vicarg@rambler.ru
俄罗斯联邦, St. Petersburg, 197376
V. Toporova
Shemyakin–Ovchinnikov Institute of Bioorganic Chemistry
Email: vicarg@rambler.ru
俄罗斯联邦, Moscow, 117997
D. Dolgikh
Department of Bioengineering, Faculty of Biology; Shemyakin–Ovchinnikov Institute of Bioorganic Chemistry
Email: vicarg@rambler.ru
俄罗斯联邦, Moscow, 119234; Moscow, 117997
P. Sveshnikov
Russian Research Center for Molecular Diagnostics and Therapy
Email: vicarg@rambler.ru
俄罗斯联邦, Moscow, 117149
V. Vasin
Research Institute of Influenza
Email: vicarg@rambler.ru
俄罗斯联邦, St. Petersburg, 197376
M. Kirpichnikov
Department of Bioengineering, Faculty of Biology; Shemyakin–Ovchinnikov Institute of Bioorganic Chemistry
Email: vicarg@rambler.ru
俄罗斯联邦, Moscow, 119234; Moscow, 117997
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