Literature DB >> 27997338

The EB66® cell line as a valuable cell substrate for MVA-based vaccines production.

Arnaud Léon1, Anne-Laure David2, Brice Madeline2, Laurence Guianvarc'h2, Elodie Dureau2, Patrick Champion-Arnaud2, Matthias Hebben2, Thierry Huss3, Benoît Chatrenet4, Klaus Schwamborn2.   

Abstract

The selection of a cell substrate is a critical step for the development and manufacturing of a viral vaccine candidate. Several parameters such as cell susceptibility and permissiveness to the viral pathogens but also performance in terms of viral antigens quality and production yields are important considerations when identifying the ideal match between a viral vaccine and cell substrate. The modified vaccinia virus Ankara (MVA) is a replication-deficient viral vector that holds great promise as a vaccine platform, however only limited cell substrates have been tested or are available for industrialization. Here we evaluate the duck embryo-derived EB66® cell line as potential cell substrate for MVA production. To this end, we used two recombinant MVA constructs and demonstrated that EB66® cells are propagating the tested MVA viruses very efficiently, while preserving viral attenuation and transgene expression for up to 20 serial passages. Furthermore we developed upstream and downstream processes that enable industrialization of the virus production. In conclusion, we showed that EB66® cells can be used as potent cell substrate for MVA-based vaccines and represent therefore an attractive alternative for vaccine production.
Copyright © 2016. Published by Elsevier Ltd.

Entities:  

Keywords:  EB66® cells; Manufacturing process; Modified vaccinia virus Ankara; Vaccine production

Mesh:

Substances:

Year:  2016        PMID: 27997338     DOI: 10.1016/j.vaccine.2016.10.043

Source DB:  PubMed          Journal:  Vaccine        ISSN: 0264-410X            Impact factor:   3.641


  4 in total

1.  The vaccinia virus based Sementis Copenhagen Vector vaccine against Zika and chikungunya is immunogenic in non-human primates.

Authors:  Natalie A Prow; Liang Liu; Mary K McCarthy; Kevin Walters; Raj Kalkeri; Jillian Geiger; Fusataka Koide; Tamara H Cooper; Preethi Eldi; Eri Nakayama; Kerrilyn R Diener; Paul M Howley; John D Hayball; Thomas E Morrison; Andreas Suhrbier
Journal:  NPJ Vaccines       Date:  2020-06-02       Impact factor: 7.344

2.  The vaccinia virus based Sementis Copenhagen Vector vaccine against Zika and chikungunya is immunogenic in non-human primates.

Authors:  Natalie A Prow; Liang Liu; Mary K McCarthy; Kevin Walters; Raj Kalkeri; Jillian Geiger; Fusataka Koide; Tamara H Cooper; Preethi Eldi; Eri Nakayama; Kerrilyn R Diener; Paul M Howley; John D Hayball; Thomas E Morrison; Andreas Suhrbier
Journal:  NPJ Vaccines       Date:  2020-06-02       Impact factor: 7.344

3.  Process intensification of EB66® cell cultivations leads to high-yield yellow fever and Zika virus production.

Authors:  Alexander Nikolay; Arnaud Léon; Klaus Schwamborn; Yvonne Genzel; Udo Reichl
Journal:  Appl Microbiol Biotechnol       Date:  2018-08-08       Impact factor: 4.813

4.  Three-dimensional culture of chicken primordial germ cells (cPGCs) in defined media containing the functional polymer FP003.

Authors:  Yi-Chen Chen; Wei-Che Chang; Shau-Ping Lin; Masataka Minami; Christian Jean; Hisato Hayashi; Sylvie Rival-Gervier; Tatsuro Kanaki; Shinn-Chih Wu; Bertrand Pain
Journal:  PLoS One       Date:  2018-09-21       Impact factor: 3.240

  4 in total

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