Especial Features of Immune Answer of Mice, Immunized by Different Types of Live Influenza Vaccines Candidate on Infection, Caused by Virulent Influenza Strain

Relevance. Live influenza vaccines are highly effective and currently used in the Russian Federation and the United States. Goal. To investigate especial features of immune response of mice, immunized by different types of live influenza vaccines and infected later by virulent influenza strain. Mate...

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Main Authors: S. . Markushin, W. . Kost, A. . Rtischev, I. . Akopova, I. . Koptyeva, K. . Lisovskaya
Format: Article
Language:Russian
Published: Numikom LLC 2016-10-01
Series:Эпидемиология и вакцинопрофилактика
Subjects:
Online Access:https://www.epidemvac.ru/jour/article/view/366
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author S. . Markushin
W. . Kost
A. . Rtischev
I. . Akopova
I. . Koptyeva
K. . Lisovskaya
author_facet S. . Markushin
W. . Kost
A. . Rtischev
I. . Akopova
I. . Koptyeva
K. . Lisovskaya
author_sort S. . Markushin
collection DOAJ
description Relevance. Live influenza vaccines are highly effective and currently used in the Russian Federation and the United States. Goal. To investigate especial features of immune response of mice, immunized by different types of live influenza vaccines and infected later by virulent influenza strain. Materials and methods. Mice were immunized by two types of live influenza vaccines candidate: cold-adapted (CA) reassortant, which inherited the 6 «internal» genes from the CA donor A/Krasnodar/101/35/59 (H2N2) and 2 genes encoding the surface proteins HA and NA from the virulent strain A/WSN/33 (H1N1) and site-specific mutants on the basis of A/WSN/33 strain, in the genome of which has been included mutations from genes of CA strains of influenza virus, encoding proteins of the polymerase complex. Immunized mice were then infected by a virulent A/WSN/33 strain of influenza virus. Results. It was shown that CA reassortant RKr35/WSN/33 and site-specific mutants Tr. № 5 and № 8 in contrast to the virulent A/WSN/33 strain were characterized by pronounced ts-phenotype and att-phenotype. Both types of live vaccines after two-time intranasal immunization induced in mice a relatively low level of humoral antibodies (log2 4,5 ± 1,2 - log2 6,0 ± 0,7). Despite the low level of induction of humoral response both types of live vaccines had similar marked protective efficiency. However, animals immunized with CA reassortant was characterized by a significant weight loss after infection with a virulent influenza strain (25%), while the infection of animals, immunized with site-specific mutants, by a similar dose of virulent flu strain has very little impact on their weight characteristics (8 - 13%). Conclusion. The data obtained indicate that antibodies to surface proteins of the virion, induced in the process of immunization, slightly inhibited the initial replication of the virulent strain and suggest that these differences in the symptoms of the infection depend on the characteristics of activated T-cell immunity. This circumstance could have a significant impact on metabolic processes in organism of infected animals.
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spelling doaj-art-f494736c05e545fbaa2dfb70d6fbf3e22025-08-04T13:01:59ZrusNumikom LLCЭпидемиология и вакцинопрофилактика2073-30462619-04942016-10-01155798510.31631/2073-3046-2016-15-5-79-85365Especial Features of Immune Answer of Mice, Immunized by Different Types of Live Influenza Vaccines Candidate on Infection, Caused by Virulent Influenza StrainS. . Markushin0W. . Kost1A. . Rtischev2I. . Akopova3I. . Koptyeva4K. . Lisovskaya5Mechnikov Research Institute for Vaccines and SeraMechnikov Research Institute for Vaccines and SeraMechnikov Research Institute for Vaccines and SeraMechnikov Research Institute for Vaccines and SeraMechnikov Research Institute for Vaccines and SeraMechnikov Research Institute for Vaccines and SeraRelevance. Live influenza vaccines are highly effective and currently used in the Russian Federation and the United States. Goal. To investigate especial features of immune response of mice, immunized by different types of live influenza vaccines and infected later by virulent influenza strain. Materials and methods. Mice were immunized by two types of live influenza vaccines candidate: cold-adapted (CA) reassortant, which inherited the 6 «internal» genes from the CA donor A/Krasnodar/101/35/59 (H2N2) and 2 genes encoding the surface proteins HA and NA from the virulent strain A/WSN/33 (H1N1) and site-specific mutants on the basis of A/WSN/33 strain, in the genome of which has been included mutations from genes of CA strains of influenza virus, encoding proteins of the polymerase complex. Immunized mice were then infected by a virulent A/WSN/33 strain of influenza virus. Results. It was shown that CA reassortant RKr35/WSN/33 and site-specific mutants Tr. № 5 and № 8 in contrast to the virulent A/WSN/33 strain were characterized by pronounced ts-phenotype and att-phenotype. Both types of live vaccines after two-time intranasal immunization induced in mice a relatively low level of humoral antibodies (log2 4,5 ± 1,2 - log2 6,0 ± 0,7). Despite the low level of induction of humoral response both types of live vaccines had similar marked protective efficiency. However, animals immunized with CA reassortant was characterized by a significant weight loss after infection with a virulent influenza strain (25%), while the infection of animals, immunized with site-specific mutants, by a similar dose of virulent flu strain has very little impact on their weight characteristics (8 - 13%). Conclusion. The data obtained indicate that antibodies to surface proteins of the virion, induced in the process of immunization, slightly inhibited the initial replication of the virulent strain and suggest that these differences in the symptoms of the infection depend on the characteristics of activated T-cell immunity. This circumstance could have a significant impact on metabolic processes in organism of infected animals.https://www.epidemvac.ru/jour/article/view/366вирус гриппахолодоадаптированные живые гриппозные вакциныхолодоадаптированные (ха) реассортантысайт-специфические мутантыиммунизацияфенотипические признакиinfluenza viruscold-adapted live influenza vaccinessite-specific mutantsimmunizationphenotypic markers
spellingShingle S. . Markushin
W. . Kost
A. . Rtischev
I. . Akopova
I. . Koptyeva
K. . Lisovskaya
Especial Features of Immune Answer of Mice, Immunized by Different Types of Live Influenza Vaccines Candidate on Infection, Caused by Virulent Influenza Strain
Эпидемиология и вакцинопрофилактика
вирус гриппа
холодоадаптированные живые гриппозные вакцины
холодоадаптированные (ха) реассортанты
сайт-специфические мутанты
иммунизация
фенотипические признаки
influenza virus
cold-adapted live influenza vaccines
site-specific mutants
immunization
phenotypic markers
title Especial Features of Immune Answer of Mice, Immunized by Different Types of Live Influenza Vaccines Candidate on Infection, Caused by Virulent Influenza Strain
title_full Especial Features of Immune Answer of Mice, Immunized by Different Types of Live Influenza Vaccines Candidate on Infection, Caused by Virulent Influenza Strain
title_fullStr Especial Features of Immune Answer of Mice, Immunized by Different Types of Live Influenza Vaccines Candidate on Infection, Caused by Virulent Influenza Strain
title_full_unstemmed Especial Features of Immune Answer of Mice, Immunized by Different Types of Live Influenza Vaccines Candidate on Infection, Caused by Virulent Influenza Strain
title_short Especial Features of Immune Answer of Mice, Immunized by Different Types of Live Influenza Vaccines Candidate on Infection, Caused by Virulent Influenza Strain
title_sort especial features of immune answer of mice immunized by different types of live influenza vaccines candidate on infection caused by virulent influenza strain
topic вирус гриппа
холодоадаптированные живые гриппозные вакцины
холодоадаптированные (ха) реассортанты
сайт-специфические мутанты
иммунизация
фенотипические признаки
influenza virus
cold-adapted live influenza vaccines
site-specific mutants
immunization
phenotypic markers
url https://www.epidemvac.ru/jour/article/view/366
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