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Caroline E Wagner Person1 #679762 Caroline Wagner is an Assistant Professor in the Department of the Bioengineering at McGill University. | Research Interests - Population-level models for infectious disease dynamics
- Within-host disease models informed by host physicochemistry and pathogen/biofluid interactions
- Characterization of mucus/pathogen transport and interactions
- Design and development of bio-inspired mucin mimetic material
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+Citations (3) - CitationsAjouter une citationList by: CiterankMapLink[2] The role of mucosal barriers in disease progression and transmission
En citant: Nicole A. Bustos, Katharina Ribbeck, Caroline E. Wagner Publication date: 12 August 2023 Publication info: Advanced Drug Delivery Reviews, Volume 200, 2023,
115008, ISSN 0169-409X CitĂ© par: David Price 6:20 PM 15 November 2023 GMT Citerank: (2) 701020CANMOD â PublicationsPublications by CANMOD Members144B5ACA0, 715325Pathogens859FDEF6 URL: DOI: https://doi.org/10.1016/j.addr.2023.115008
| Extrait - [Advanced Drug Delivery Reviews, 12 August 2023.]
Mucus is a biological hydrogel that coats and protects all non-keratinized wet epithelial surfaces. Mucins, the primary structural components of mucus, are critical components of the gel layer that protect against invading pathogens. For communicable diseases, pathogen-mucin interactions contribute to the pathogenâs fate and the potential for disease progression in-host, as well as the potential for onward transmission. We begin by reviewing in-host mucus filtering mechanisms, including size filtering and interaction filtering, which regulate the permeability of mucus barriers to all molecules including pathogens. Next, we discuss the role of mucins in communicable diseases at the point of transmission (i.e. how the encapsulation of pathogens in emitted mucosal droplets externally to hosts may modulate pathogen infectivity and viability). Overall, mucosal barriers modulate both host susceptibility as well as the dynamics of population-level disease transmission. The study of mucins and their use in models and experimental systems are therefore crucial for understanding the mechanistic biophysical principles underlying disease transmission and the early stages of host infection. |
Link[3] Medium-term scenarios of COVID-19 as a function of immune uncertainties and chronic disease
En citant: Chadi M. Saad-Roy, Sinead E. Morris, Rachel E. Baker, Jeremy Farrar, Andrea L. Graham, Simon A. Levin, Caroline E. Wagner, C. Jessica. E. Metcalf, Bryan T. Grenfell Publication date: 30 August 2023 Publication info: J. R. Soc. Interface.202023024720230247 CitĂ© par: David Price 0:18 AM 28 November 2023 GMT Citerank: (4) 701020CANMOD â PublicationsPublications by CANMOD Members144B5ACA0, 704036Immunology859FDEF6, 704045Covid-19859FDEF6, 715952Long covid859FDEF6 URL: DOI: https://doi.org/10.1098/rsif.2023.0247
| Extrait - [Journal of the Royal Society of Interface, 30 August 2023]
As the SARS-CoV-2 trajectory continues, the longer-term immuno-epidemiology of COVID-19, the dynamics of Long COVID, and the impact of escape variants are important outstanding questions. We examine these remaining uncertainties with a simple modelling framework that accounts for multiple (antigenic) exposures via infection or vaccination. If immunity (to infection or Long COVID) accumulates rapidly with the valency of exposure, we find that infection levels and the burden of Long COVID are markedly reduced in the medium term. More pessimistic assumptions on host adaptive immune responses illustrate that the longer-term burden of COVID-19 may be elevated for years to come. However, we also find that these outcomes could be mitigated by the eventual introduction of a vaccine eliciting robust (i.e. durable, transmission-blocking and/or âevolution-proofâ) immunity. Overall, our work stresses the wide range of future scenarios that still remain, the importance of collecting real-world epidemiological data to identify likely outcomes, and the crucial need for the development of a highly effective transmission-blocking, durable and broadly protective vaccine. |
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