Production of Influenza Virus Proteins Using Recombinant Insect Cells

Influenza vaccines have long been manufactured in embryonated chicken eggs. This method has some problems such as a long production period (about 6 months) and use of large amounts of infectious pathogens. Recently, the production of recombinant subunit vaccines using the baculovirus–insect cell sys...

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Main Authors: Matsuda Takuya, Tanijima Toshikazu, Masumi-Koizumi Kyoko, Katsuda Tomohisa, Yamaji Hideki
Format: Article
Language:English
Published: EDP Sciences 2021-01-01
Series:MATEC Web of Conferences
Online Access:https://www.matec-conferences.org/articles/matecconf/pdf/2021/02/matecconf_apcche21_07009.pdf
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spelling doaj-3e9649d354964a9a86a698ce1efd89af2021-01-15T10:19:30ZengEDP SciencesMATEC Web of Conferences2261-236X2021-01-013330700910.1051/matecconf/202133307009matecconf_apcche21_07009Production of Influenza Virus Proteins Using Recombinant Insect CellsMatsuda TakuyaTanijima ToshikazuMasumi-Koizumi KyokoKatsuda TomohisaYamaji HidekiInfluenza vaccines have long been manufactured in embryonated chicken eggs. This method has some problems such as a long production period (about 6 months) and use of large amounts of infectious pathogens. Recently, the production of recombinant subunit vaccines using the baculovirus–insect cell system has been extensively investigated. In this system, viral immunodominant components can be produced more rapidly and in a larger scale than in the conventional egg-based process. However, continuous production is virtually impossible because infection of recombinant baculovirus results in the death of host insect cells. In the present study, we established stably transformed insect cells that secreted influenza virus-like particles (VLPs) consisting of hemagglutinin (HA), the major protective antigen of influenza A virus, and matrix protein 1 (M1), another structural protein of the virus. Hemagglutination assay and transmission electron microscopy (TEM) suggested that HA produced by recombinant insect cells kept the hemagglutination activity and the morphology of the VLPs was similar to that of wild type influenza virus particles.https://www.matec-conferences.org/articles/matecconf/pdf/2021/02/matecconf_apcche21_07009.pdf
collection DOAJ
language English
format Article
sources DOAJ
author Matsuda Takuya
Tanijima Toshikazu
Masumi-Koizumi Kyoko
Katsuda Tomohisa
Yamaji Hideki
spellingShingle Matsuda Takuya
Tanijima Toshikazu
Masumi-Koizumi Kyoko
Katsuda Tomohisa
Yamaji Hideki
Production of Influenza Virus Proteins Using Recombinant Insect Cells
MATEC Web of Conferences
author_facet Matsuda Takuya
Tanijima Toshikazu
Masumi-Koizumi Kyoko
Katsuda Tomohisa
Yamaji Hideki
author_sort Matsuda Takuya
title Production of Influenza Virus Proteins Using Recombinant Insect Cells
title_short Production of Influenza Virus Proteins Using Recombinant Insect Cells
title_full Production of Influenza Virus Proteins Using Recombinant Insect Cells
title_fullStr Production of Influenza Virus Proteins Using Recombinant Insect Cells
title_full_unstemmed Production of Influenza Virus Proteins Using Recombinant Insect Cells
title_sort production of influenza virus proteins using recombinant insect cells
publisher EDP Sciences
series MATEC Web of Conferences
issn 2261-236X
publishDate 2021-01-01
description Influenza vaccines have long been manufactured in embryonated chicken eggs. This method has some problems such as a long production period (about 6 months) and use of large amounts of infectious pathogens. Recently, the production of recombinant subunit vaccines using the baculovirus–insect cell system has been extensively investigated. In this system, viral immunodominant components can be produced more rapidly and in a larger scale than in the conventional egg-based process. However, continuous production is virtually impossible because infection of recombinant baculovirus results in the death of host insect cells. In the present study, we established stably transformed insect cells that secreted influenza virus-like particles (VLPs) consisting of hemagglutinin (HA), the major protective antigen of influenza A virus, and matrix protein 1 (M1), another structural protein of the virus. Hemagglutination assay and transmission electron microscopy (TEM) suggested that HA produced by recombinant insect cells kept the hemagglutination activity and the morphology of the VLPs was similar to that of wild type influenza virus particles.
url https://www.matec-conferences.org/articles/matecconf/pdf/2021/02/matecconf_apcche21_07009.pdf
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