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Estimates of the collective immunity to COVID-19 derived from a stochastic cellular automaton based framework
In the context of the propagation of infectious diseases, when a sufficient degree of immunisation is achieved within a population, the spread of the disease is ended or significantly decreased, leading to collective immunity, meaning the indirect protection given by immune individuals to susceptibl...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9206103/ https://www.ncbi.nlm.nih.gov/pubmed/35757184 http://dx.doi.org/10.1007/s11047-022-09893-3 |
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author | Lima, Isaías Balbi, Pedro Paulo |
author_facet | Lima, Isaías Balbi, Pedro Paulo |
author_sort | Lima, Isaías |
collection | PubMed |
description | In the context of the propagation of infectious diseases, when a sufficient degree of immunisation is achieved within a population, the spread of the disease is ended or significantly decreased, leading to collective immunity, meaning the indirect protection given by immune individuals to susceptible individuals. Here we describe the estimates of the collective immunity to COVID-19 from a stochastic cellular automaton based model designed to emulate the spread of SARS-CoV-2 in a population of static individuals interacting only via a Moore neighbourhood of radius one, with a view to analyze the impact of initially immune individuals on the dynamics of COVID-19. This impact was measured by comparing a progression of initial immunity ratio—the percentage of immunised individuals before patient zero starts infecting its neighbourhood—from 0 to 95% of the initial population, with the number of susceptible individuals not contaminated, the peak value of active cases, the total number of deaths and the emulated pandemic duration in days. The influence of this range of immunities over the model was tested with different parameterisations regarding the uncertainties involved in the model such as the durations of the cellular automaton states, the contamination contributions of each state and the state transition probabilities. A collective immunity threshold of [Formula: see text] on average was obtained from this procedure, under four distinct parameterisations, which is in tune with the estimates of the currently available medical literature, even increasing the uncertainty of the input parameters. |
format | Online Article Text |
id | pubmed-9206103 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-92061032022-06-21 Estimates of the collective immunity to COVID-19 derived from a stochastic cellular automaton based framework Lima, Isaías Balbi, Pedro Paulo Nat Comput Article In the context of the propagation of infectious diseases, when a sufficient degree of immunisation is achieved within a population, the spread of the disease is ended or significantly decreased, leading to collective immunity, meaning the indirect protection given by immune individuals to susceptible individuals. Here we describe the estimates of the collective immunity to COVID-19 from a stochastic cellular automaton based model designed to emulate the spread of SARS-CoV-2 in a population of static individuals interacting only via a Moore neighbourhood of radius one, with a view to analyze the impact of initially immune individuals on the dynamics of COVID-19. This impact was measured by comparing a progression of initial immunity ratio—the percentage of immunised individuals before patient zero starts infecting its neighbourhood—from 0 to 95% of the initial population, with the number of susceptible individuals not contaminated, the peak value of active cases, the total number of deaths and the emulated pandemic duration in days. The influence of this range of immunities over the model was tested with different parameterisations regarding the uncertainties involved in the model such as the durations of the cellular automaton states, the contamination contributions of each state and the state transition probabilities. A collective immunity threshold of [Formula: see text] on average was obtained from this procedure, under four distinct parameterisations, which is in tune with the estimates of the currently available medical literature, even increasing the uncertainty of the input parameters. Springer Netherlands 2022-06-18 2022 /pmc/articles/PMC9206103/ /pubmed/35757184 http://dx.doi.org/10.1007/s11047-022-09893-3 Text en © The Author(s), under exclusive licence to Springer Nature B.V. 2022 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Article Lima, Isaías Balbi, Pedro Paulo Estimates of the collective immunity to COVID-19 derived from a stochastic cellular automaton based framework |
title | Estimates of the collective immunity to COVID-19 derived from a stochastic cellular automaton based framework |
title_full | Estimates of the collective immunity to COVID-19 derived from a stochastic cellular automaton based framework |
title_fullStr | Estimates of the collective immunity to COVID-19 derived from a stochastic cellular automaton based framework |
title_full_unstemmed | Estimates of the collective immunity to COVID-19 derived from a stochastic cellular automaton based framework |
title_short | Estimates of the collective immunity to COVID-19 derived from a stochastic cellular automaton based framework |
title_sort | estimates of the collective immunity to covid-19 derived from a stochastic cellular automaton based framework |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9206103/ https://www.ncbi.nlm.nih.gov/pubmed/35757184 http://dx.doi.org/10.1007/s11047-022-09893-3 |
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