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Live-attenuated influenza vaccines based on premature termination | 59059
Journal of Infectious Diseases & Preventive Medicine

Journal of Infectious Diseases & Preventive Medicine
Open Access

ISSN: 2329-8731

Live-attenuated influenza vaccines based on premature termination codon (PTC)- harboring viruses


Joint Event on Infection Congress 2020 & Tropical Diseases 2020

February 24-25, 2020 | Berlin, Germany

Huan Xu

North China Pharmaceutical Company, China

Scientific Tracks Abstracts: J Infect Dis Prev Med

Abstract :

The conversion of life-threatening viruses into live but avirulent vaccines represents a revolution in vaccinology. In a proof-of-principle study, we expanded the genetic code of the genome of influenza a virus via a transgenic cell line containing orthogonal translation machinery. This generated premature termination codon (PTC)–harboring viruses that exerted full infectivity but were replication-incompetent in conventional cells. Genome-wide optimization of the sites for incorporation of multiple PTCs resulted in highly reproductive and genetically stable progeny viruses in transgenic cells. In mouse, ferret and guinea pig models vaccination with PTC viruses elicited robust humoral, mucosal and T cell-mediated immunity against antigenically distinct influenza viruses and even neutralized existing infecting strains. The methods presented here may become a general approach for generating live virus vaccines that can be adapted to almost any virus.
Recent Publications:
• Longlong S and Huan X (2016) Generation of influenza a viruses as live but replication-incompetent virus vaccines. Science 354(6316):1170-1173.
• Huan X (2016) Re-exploration of the codon context effect on amber codon-guided incorporation of noncanonical amino acids in E. coli by the blue-white screening assay. ChemBioChem. 17(13):1250-1256.
• Bo Z and Huan X (2015) development of next generation of therapeutic IFN-alpha2b via genetic code expansion. Acta Biomater. 19:100-111.
• Ziwei Z and Huan X (2017) Construction of an inducible stable cell line for efficient incorporation of unnatural amino acids in mammalian cells. BBRC 489(4):490-496.
• Yongxiang Z, Fei Y, Yiming W, Longlong S and Huan X (2015) Broaden the versatility of lentiviral vector as a tool in nucleic acid research via genetic code expansion. Nucleic Acids Res., 43(11):e73.

Biography :

Huan Xu has her expertise in discovery of new biotechnology drugs including recombinant long-lasting protein, bispecific antibody and vaccines. She received her bachelor and doctoral degree both from Peking University. After graduation, she joined the North China Pharmaceutical Company as a senior scientist. The methods presented here utilize expansion of the genetic code (Lei Wang 2001) of influenza a virus. It may become a general approach for generating live virus vaccines.

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