Novel coronavirus SARS-CoV-2 (Covid-19) dynamics inside the human body.
Acute-Phase Proteins
/ antagonists & inhibitors
Angiotensin-Converting Enzyme 2
Anti-Inflammatory Agents
/ therapeutic use
Antiviral Agents
/ therapeutic use
Betacoronavirus
/ drug effects
Body Temperature
COVID-19
Coronavirus Infections
/ drug therapy
Cytokines
/ antagonists & inhibitors
Epithelial Cells
/ drug effects
Gene Expression Regulation
Host-Pathogen Interactions
/ drug effects
Humans
Lung
/ drug effects
Macrophages, Alveolar
/ drug effects
Nonlinear Dynamics
Pandemics
Peptidyl-Dipeptidase A
/ genetics
Pneumonia, Viral
/ drug therapy
Pulmonary Gas Exchange
/ drug effects
SARS-CoV-2
Spike Glycoprotein, Coronavirus
/ antagonists & inhibitors
Covid-19
cybernetics
gas exchange
inflammatory mediators
pressure difference
thermostat
Journal
Reviews in medical virology
ISSN: 1099-1654
Titre abrégé: Rev Med Virol
Pays: England
ID NLM: 9112448
Informations de publication
Date de publication:
09 2020
09 2020
Historique:
received:
20
05
2020
revised:
14
06
2020
accepted:
16
06
2020
pubmed:
21
7
2020
medline:
2
10
2020
entrez:
21
7
2020
Statut:
ppublish
Résumé
A knowledge-based cybernetic framework model representing the dynamics of SARS-CoV-2 inside the human body has been studied analytically and in silico to explore the pathophysiologic regulations. The following modeling methodology was developed as a platform to introduce a predictive tool supporting a therapeutic approach to Covid-19 disease. A time-dependent nonlinear system of ordinary differential equations model was constructed involving type-I cells, type-II cells, SARS-CoV-2 virus, inflammatory mediators, interleukins along with host pulmonary gas exchange rate, thermostat control, and mean pressure difference. This formalism introduced about 17 unknown parameters. Estimating these unknown parameters requires a mathematical association with the in vivo sparse data and the dynamic sensitivities of the model. The cybernetic model can simulate a dynamic response to the reduced pulmonary alveolar gas exchange rate, thermostat control, and mean pressure difference under a very critical condition based on equilibrium (steady state) values of the inflammatory mediators and system parameters. In silico analysis of the current cybernetical approach with system dynamical modeling can provide an intellectual framework to help experimentalists identify more active therapeutic approaches.
Identifiants
pubmed: 32686248
doi: 10.1002/rmv.2140
pmc: PMC7404608
doi:
Substances chimiques
Acute-Phase Proteins
0
Anti-Inflammatory Agents
0
Antiviral Agents
0
Cytokines
0
Spike Glycoprotein, Coronavirus
0
spike protein, SARS-CoV-2
0
Peptidyl-Dipeptidase A
EC 3.4.15.1
ACE2 protein, human
EC 3.4.17.23
Angiotensin-Converting Enzyme 2
EC 3.4.17.23
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
e2140Subventions
Organisme : University College London
Pays : International
Organisme : World Health Organization
Pays : International
Informations de copyright
© 2020 John Wiley & Sons, Ltd.
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