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2554. Safety and Immunogenicity of NasoVAX, a Novel Intranasal Influenza Vaccine

BACKGROUND: NasoVAX is a replication-deficient adenovirus-based vaccine designed to express influenza hemagglutinin in nasal epithelial cells when given as a nasal spray. In preclinical studies, NasoVAX was associated with divergent strain protection. Prior preclinical and clinical studies with the...

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Autores principales: Tasker, Sybil, Krishnan, Vyjayanthi, Bart, Stephan, Suyundikov, Anvar, Booth, Peta-Gay, Wight O’Rourke, Anna, Zhang, Jianfeng, Georges, Bertrand, Roberts, Scot
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253025/
http://dx.doi.org/10.1093/ofid/ofy209.162
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author Tasker, Sybil
Krishnan, Vyjayanthi
Bart, Stephan
Suyundikov, Anvar
Booth, Peta-Gay
Wight O’Rourke, Anna
Zhang, Jianfeng
Georges, Bertrand
Roberts, Scot
author_facet Tasker, Sybil
Krishnan, Vyjayanthi
Bart, Stephan
Suyundikov, Anvar
Booth, Peta-Gay
Wight O’Rourke, Anna
Zhang, Jianfeng
Georges, Bertrand
Roberts, Scot
author_sort Tasker, Sybil
collection PubMed
description BACKGROUND: NasoVAX is a replication-deficient adenovirus-based vaccine designed to express influenza hemagglutinin in nasal epithelial cells when given as a nasal spray. In preclinical studies, NasoVAX was associated with divergent strain protection. Prior preclinical and clinical studies with the vector demonstrated lack of impact from baseline adenovirus immunity. METHODS: Sixty healthy adults were randomized to an A/California 2009-based monovalent NasoVAX formulation at doses of 10(9), 10(10), or 10(11) viral particles or saline placebo, all given as a 0.25 mL nasal spray in each nostril. Subjects were followed for safety, including solicited local and systemic side effects. Immune measures included hemagglutination inhibition (HAI) and neutralizing antibody (MN) at days 1, 15, 29, 90, and 180, and γ-interferon ELISpot at day 1 and 8. A parallel cohort of 20 similar subjects were dosed with Fluzone® injectable influenza vaccine containing an A/California 2009 component and had assessments at the same timepoints. The laboratory was blind to treatment assignment for these comparator samples. RESULTS: NasoVAX was well tolerated with no serious adverse events and no fever. Solicited symptoms such as nasal congestion, sore throat, and headache did not increase with dose and were not statistically different than placebo. Available immune response data are shown below. CONCLUSION: NasoVAX intranasal influenza vaccine was well tolerated and elicited comparable antibody responses and nearly 6-fold higher cellular immune responses than a licensed injectable vaccine. DISCLOSURES: S. Tasker, Altimmune, Inc: Employee and Shareholder, Salary. V. Krishnan, Altimmune, Inc.: Employee and Shareholder, Salary. S. Bart, Altimmune, Inc.: Research Contractor, fee for research services. A. Suyundikov, Altimmune, Inc.: Employee, Salary. P. G. Booth, Altimmune, Inc.: Research Contractor, fee for research services. A. Wight O’Rourke, Altimmune, Inc.: Employee and Shareholder, Salary. J. Zhang, Altimmune, Inc.: Employee and Shareholder, Salary. B. Georges, Altimmune, Inc.: Employee and Shareholder, Salary. S. Roberts, Altimmune, Inc.: Employee and Shareholder, Salary.
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spelling pubmed-62530252018-11-28 2554. Safety and Immunogenicity of NasoVAX, a Novel Intranasal Influenza Vaccine Tasker, Sybil Krishnan, Vyjayanthi Bart, Stephan Suyundikov, Anvar Booth, Peta-Gay Wight O’Rourke, Anna Zhang, Jianfeng Georges, Bertrand Roberts, Scot Open Forum Infect Dis Abstracts BACKGROUND: NasoVAX is a replication-deficient adenovirus-based vaccine designed to express influenza hemagglutinin in nasal epithelial cells when given as a nasal spray. In preclinical studies, NasoVAX was associated with divergent strain protection. Prior preclinical and clinical studies with the vector demonstrated lack of impact from baseline adenovirus immunity. METHODS: Sixty healthy adults were randomized to an A/California 2009-based monovalent NasoVAX formulation at doses of 10(9), 10(10), or 10(11) viral particles or saline placebo, all given as a 0.25 mL nasal spray in each nostril. Subjects were followed for safety, including solicited local and systemic side effects. Immune measures included hemagglutination inhibition (HAI) and neutralizing antibody (MN) at days 1, 15, 29, 90, and 180, and γ-interferon ELISpot at day 1 and 8. A parallel cohort of 20 similar subjects were dosed with Fluzone® injectable influenza vaccine containing an A/California 2009 component and had assessments at the same timepoints. The laboratory was blind to treatment assignment for these comparator samples. RESULTS: NasoVAX was well tolerated with no serious adverse events and no fever. Solicited symptoms such as nasal congestion, sore throat, and headache did not increase with dose and were not statistically different than placebo. Available immune response data are shown below. CONCLUSION: NasoVAX intranasal influenza vaccine was well tolerated and elicited comparable antibody responses and nearly 6-fold higher cellular immune responses than a licensed injectable vaccine. DISCLOSURES: S. Tasker, Altimmune, Inc: Employee and Shareholder, Salary. V. Krishnan, Altimmune, Inc.: Employee and Shareholder, Salary. S. Bart, Altimmune, Inc.: Research Contractor, fee for research services. A. Suyundikov, Altimmune, Inc.: Employee, Salary. P. G. Booth, Altimmune, Inc.: Research Contractor, fee for research services. A. Wight O’Rourke, Altimmune, Inc.: Employee and Shareholder, Salary. J. Zhang, Altimmune, Inc.: Employee and Shareholder, Salary. B. Georges, Altimmune, Inc.: Employee and Shareholder, Salary. S. Roberts, Altimmune, Inc.: Employee and Shareholder, Salary. Oxford University Press 2018-11-26 /pmc/articles/PMC6253025/ http://dx.doi.org/10.1093/ofid/ofy209.162 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Abstracts
Tasker, Sybil
Krishnan, Vyjayanthi
Bart, Stephan
Suyundikov, Anvar
Booth, Peta-Gay
Wight O’Rourke, Anna
Zhang, Jianfeng
Georges, Bertrand
Roberts, Scot
2554. Safety and Immunogenicity of NasoVAX, a Novel Intranasal Influenza Vaccine
title 2554. Safety and Immunogenicity of NasoVAX, a Novel Intranasal Influenza Vaccine
title_full 2554. Safety and Immunogenicity of NasoVAX, a Novel Intranasal Influenza Vaccine
title_fullStr 2554. Safety and Immunogenicity of NasoVAX, a Novel Intranasal Influenza Vaccine
title_full_unstemmed 2554. Safety and Immunogenicity of NasoVAX, a Novel Intranasal Influenza Vaccine
title_short 2554. Safety and Immunogenicity of NasoVAX, a Novel Intranasal Influenza Vaccine
title_sort 2554. safety and immunogenicity of nasovax, a novel intranasal influenza vaccine
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253025/
http://dx.doi.org/10.1093/ofid/ofy209.162
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