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DOI 10.1016/j.vaccine.2014.07.092

Медицинская библиотека · Vaccine · 2014

Characterization and immunogenicity in mice of recombinant influenza haemagglutinins produced in Leishmania tarentolae.

Pion Corinne, Courtois Virginie, Husson Stéphanie, Bernard Marie-Clotilde, Nicolai Marie-Claire, Talaga Philippe, Trannoy Emanuelle, Moste Catherine, Sodoyer Régis, Legastelois Isabelle

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

The membrane displayed antigen haemagglutinin (HA) from several influenza strains were expressed in the Leishmania tarentolae system. This non-conventional expression system based on a parasite of lizards, can be readily propagated to high cell density (>10(8)cells/mL) in a simple incubator at 26°C. The genes encoding HA proteins were cloned from six influenza strains, among these being a 2009 A/H1N1 pandemic strain from swine origin, namely A/California/07/09(H1N1). Soluble HA proteins were secreted into the cell culture medium and were easily and successfully purified via a His-Tag domain fused to the proteins. The overall process could be conducted in less than 3 months and resulted in a yield of approximately 1.5-5mg of HA per liter of biofermenter culture after purification. The recombinant HA proteins expressed by L. tarentolae were characterized by dynamic light scattering and were observed to be mostly monomeric. The L. tarentolae recombinant HA proteins were immunogenic in mice at a dose of 10μg when administered twice with an oil-in-water emulsion-based adjuvant. These results suggest that the L. tarentolae expression system may be an alternative to the current egg-based vaccine production.

Для цитирования: Pion Corinne, Courtois Virginie, Husson Stéphanie, Bernard Marie-Clotilde, Nicolai Marie-Claire, Talaga Philippe, Trannoy Emanuelle, Moste Catherine, Sodoyer Régis, Legastelois Isabelle. Characterization and immunogenicity in mice of recombinant influenza haemagglutinins produced in Leishmania tarentolae.. Vaccine. 2014. DOI: 10.1016/j.vaccine.2014.07.092.

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