Fiona Smaill

Fiona Smaill


Research Focus & Metrics

Academic Career Length

31Years (1996-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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28 October 2014 in Cochrane Database of Systematic Reviews
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Journal Article
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FSFiona Smaill
Fiona Smaill
RGRosalie M Grivell
Rosalie M Grivell

24 September 2008 in European Journal of Clinical Investigation
Verified
Journal Article
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JSJ. Schnarr
J. Schnarr
FSFiona Smaill
Fiona Smaill

18 April 2007
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Reference Entry
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FSFiona Smaill
Fiona Smaill
JVJuan C Vazquez
Juan C Vazquez

25 November 2019 in Cochrane Database of Systematic Reviews
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Journal Article
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FSFiona Smaill
Fiona Smaill
JVJuan C Vazquez
Juan C Vazquez

7 August 2015 in Cochrane Database of Systematic Reviews
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Journal Article
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FSFiona Smaill
Fiona Smaill
JVJuan C Vazquez
Juan C Vazquez

8 February 2022 in JCI Insight
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Journal Article
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MJMangalakumari Jeyanathan
Mangalakumari Jeyanathan
DFDominik K. Fritz
Dominik K. Fritz
SASam Afkhami
Sam Afkhami
EAEmilio Aguirre
Emilio Aguirre
KHKaren J. Howie
Karen J. Howie
FSFiona Smaill
Fiona Smaill
Background: Adenovirus-vectored (Ad-vectored) vaccines are typically administered via i.m. injection to humans and are incapable of inducing respiratory mucosal immunity. However, aerosol delivery of Ad-vectored vaccines remains poorly characterized, and its ability to induce mucosal immunity in humans is unknown. This phase Ib trial evaluated the safety and immunogenicity of human serotype-5 Ad-vectored tuberculosis (TB) vaccine (AdHu5Ag85A) delivered to humans via inhaled aerosol or i.m. injection. Methods: Thirty-one healthy, previously BCG-vaccinated adults were enrolled. AdHu5Ag85A was administered by single-dose aerosol using Aeroneb Solo Nebulizer or by i.m. injection. The study consisted of the low-dose (LD) aerosol, high-dose (HD) aerosol, and i.m. groups. The adverse events were assessed at various times after vaccination. Immunogenicity data were collected from the peripheral blood and bronchoalveolar lavage samples at baseline, as well as at select time points after vaccination. Results: The nebulized aerosol droplets were < 5.39 μm in size. Both LD and HD of AdHu5Ag85A administered by aerosol inhalation and i.m. injection were safe and well tolerated. Both aerosol doses, particularly LD, but not i.m., vaccination markedly induced airway tissue–resident memory CD4 + and CD8 + T cells of polyfunctionality. While as expected, i.m. vaccination induced Ag85A-specific T cell responses in the blood, the LD aerosol vaccination also elicited such T cells in the blood. Furthermore, the LD aerosol vaccination induced persisting transcriptional changes in alveolar macrophages. Conclusion: Inhaled aerosol delivery of Ad-vectored vaccine is a safe and superior way to elicit respiratory mucosal immunity. This study warrants further development of aerosol vaccine strategies against respiratory pathogens, including TB and COVID-19. Trial registration: ClinicalTrial.gov, NCT02337270. Funding: The Canadian Institutes for Health Research (CIHR) and the Natural Sciences and Engineering Research Council of Canada funded this work.