Autocrine and paracrine interferon signalling as ‘ring vaccination’ and ‘contact tracing’ strategies to suppress virus infection in a host
Abstract
The innate immune response, particularly the interferon response, represents a first line of defence against viral infections. The interferon molecules produced from infected cells act through autocrine and paracrine signalling to turn host cells into an antiviral state. Although the molecular mechanisms of IFN signalling have been well characterized, how the interferon response collectively contribute to the regulation of host cells to stop or suppress viral infection during early infection remain unclear. Here, we use mathematical models to delineate the roles of the autocrine and the paracrine signalling, and show that their impacts on viral spread are dependent on how infection proceeds. In particular, we found that when infection is well-mixed, the paracrine signalling is not as effective; by contrast, when infection spreads in a spatial manner, a likely scenario during initial infection in tissue, the paracrine signalling can impede the spread of infection by decreasing the number of susceptible cells close to the site of infection. Furthermore, we argue that the interferon response can be seen as a parallel to population-level epidemic prevention strategies such as ‘contact tracing’ or ‘ring vaccination’. Thus, our results here may have implications for the outbreak control at the population scale more broadly.
- Authors:
-
- North Carolina State Univ., Raleigh, NC (United States). Dept. of Mathematics
- North Carolina State Univ., Raleigh, NC (United States). School of Veterinary Medicine
- North Carolina State Univ., Raleigh, NC (United States). Dept. of Mathematics; Los Alamos National Lab. (LANL), Los Alamos, NM (United States). Theoretical Biology and Biophysics
- Publication Date:
- Research Org.:
- Triad National Security, LLC, Los Alamos, NM (United States); Los Alamos National Lab. (LANL), Los Alamos, NM (United States)
- Sponsoring Org.:
- USDOE National Nuclear Security Administration (NNSA)
- OSTI Identifier:
- 1815801
- Grant/Contract Number:
- 89233218CNA000001
- Resource Type:
- Accepted Manuscript
- Journal Name:
- Proceedings of the Royal Society B: Biological Sciences
- Additional Journal Information:
- Journal Volume: 288; Journal Issue: 1945; Journal ID: ISSN 0962-8452
- Publisher:
- The Royal Society Publishing
- Country of Publication:
- United States
- Language:
- English
- Subject:
- 59 BASIC BIOLOGICAL SCIENCES; interferon; innate immunity; ring vaccination; partial differential equations; cellular automata
Citation Formats
Michael Lavigne, G., Russell, Hayley, Sherry, Barbara, and Ke, Ruian. Autocrine and paracrine interferon signalling as ‘ring vaccination’ and ‘contact tracing’ strategies to suppress virus infection in a host. United States: N. p., 2021.
Web. doi:10.1098/rspb.2020.3002.
Michael Lavigne, G., Russell, Hayley, Sherry, Barbara, & Ke, Ruian. Autocrine and paracrine interferon signalling as ‘ring vaccination’ and ‘contact tracing’ strategies to suppress virus infection in a host. United States. https://doi.org/10.1098/rspb.2020.3002
Michael Lavigne, G., Russell, Hayley, Sherry, Barbara, and Ke, Ruian. Wed .
"Autocrine and paracrine interferon signalling as ‘ring vaccination’ and ‘contact tracing’ strategies to suppress virus infection in a host". United States. https://doi.org/10.1098/rspb.2020.3002. https://www.osti.gov/servlets/purl/1815801.
@article{osti_1815801,
title = {Autocrine and paracrine interferon signalling as ‘ring vaccination’ and ‘contact tracing’ strategies to suppress virus infection in a host},
author = {Michael Lavigne, G. and Russell, Hayley and Sherry, Barbara and Ke, Ruian},
abstractNote = {The innate immune response, particularly the interferon response, represents a first line of defence against viral infections. The interferon molecules produced from infected cells act through autocrine and paracrine signalling to turn host cells into an antiviral state. Although the molecular mechanisms of IFN signalling have been well characterized, how the interferon response collectively contribute to the regulation of host cells to stop or suppress viral infection during early infection remain unclear. Here, we use mathematical models to delineate the roles of the autocrine and the paracrine signalling, and show that their impacts on viral spread are dependent on how infection proceeds. In particular, we found that when infection is well-mixed, the paracrine signalling is not as effective; by contrast, when infection spreads in a spatial manner, a likely scenario during initial infection in tissue, the paracrine signalling can impede the spread of infection by decreasing the number of susceptible cells close to the site of infection. Furthermore, we argue that the interferon response can be seen as a parallel to population-level epidemic prevention strategies such as ‘contact tracing’ or ‘ring vaccination’. Thus, our results here may have implications for the outbreak control at the population scale more broadly.},
doi = {10.1098/rspb.2020.3002},
journal = {Proceedings of the Royal Society B: Biological Sciences},
number = 1945,
volume = 288,
place = {United States},
year = {Wed Feb 24 00:00:00 EST 2021},
month = {Wed Feb 24 00:00:00 EST 2021}
}
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