Modelling the effectiveness of antiviral treatment strategies to prevent household transmission of acute respiratory viruses.

Publication date: Dec 01, 2024

Households are a major driver of transmission of acute respiratory viruses, such as SARS-CoV-2 or Influenza. Until now antiviral treatments have mostly been used as a curative treatment in symptomatic individuals. During an outbreak, more aggressive strategies involving pre- or post-exposure prophylaxis (PrEP or PEP) could be employed to further reduce the risk of severe disease but also prevent transmission to household contacts. In order to understand the effectiveness of such strategies and the factors that may modulate them, we developed a multi-scale model that follows the infection at both the individual-level (viral dynamics) and the population-level (transmission dynamics) in households. Using a simulation study we explored different antiviral treatment strategies, evaluating their effectiveness on reducing the transmission risk and the virological burden in households for a range of virus characteristics (e. g., secondary attack rate-SAR, or time to peak viral load). We found that when the index case can be identified and treated before symptom onset, both transmission and virological burden are reduced by > 75% for most SAR values and time to peak viral load, with minimal benefit to treat additionally household contacts. While treatment initiated after index symptom onset does not reduce the risk of transmission, it can still reduce the virological burden in the household, a proxy for severe disease and subsequent transmission risk outside the household. In that case optimal strategies involve treatment of both index case and household contacts as PEP, with efficacy > 50% when peak viral load occurs after symptom onset, and 30-50% otherwise. In all the considered cases, antiviral treatment strategies were optimal for SAR ranging 20-60%, and for larger household sizes. This study highlights the opportunity of antiviral drug-based interventions in households during an outbreak to minimize viral transmission and disease burden.

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Concepts Keywords
Antiviral Antiviral Agents
Curative Antiviral Agents
Driver Computational Biology
Viruses Computer Simulation
COVID-19
COVID-19 Drug Treatment
Family Characteristics
Humans
Influenza, Human
Post-Exposure Prophylaxis
SARS-CoV-2
Viral Load

Semantics

Type Source Name
disease MESH Influenza
disease MESH infection
disease MESH viral load
disease IDO symptom
drug DRUGBANK Trestolone
drug DRUGBANK Etodolac
disease IDO history
disease IDO process
pathway REACTOME Reproduction
drug DRUGBANK Coenzyme M
disease MESH viral infections
disease MESH community transmission
drug DRUGBANK Diethylstilbestrol
disease IDO intervention
drug DRUGBANK Tropicamide
disease IDO contact tracing
disease IDO host
disease IDO immune response
disease IDO infected population
drug DRUGBANK Aspartame
disease IDO production
pathway KEGG Viral replication
disease MESH reinfection
disease MESH secondary infections
disease MESH viral shedding
drug DRUGBANK Methylergometrine
disease IDO contagiousness
drug DRUGBANK Ranitidine
disease IDO pathogen
disease MESH over treatment
drug DRUGBANK Methionine
disease MESH SARS CoV 2 infection
disease MESH Emerging infectious diseases
drug DRUGBANK Ritonavir
disease MESH Infectious Diseases
disease MESH Opportunistic Infections
drug DRUGBANK Guanosine
disease IDO susceptibility
disease IDO infectivity
drug DRUGBANK Hydroxychloroquine

Original Article

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