Interactions between respiratory viruses in US adults and children: a prospective cohort study
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Background
The relationship between recent viral infection and subsequent susceptibility to, or protection against, other viruses remains unclear, particularly across age groups and symptom status.
Methods
A prospective cohort study enrolled participants aged 6 months to 49 years in Washington and Oregon, USA, 2022–2024. Weekly nasal swabs were tested for SARS-CoV-2, respiratory syncytial virus (RSV), and influenza A/B; additional swabs were collected during symptomatic illness and were also tested for parainfluenza (PIV) 1–4, endemic human coronaviruses (hCOV), adenovirus, human metapneumovirus, human rhinovirus (hRV), and enteroviruses. Proportional hazards regression models were used to characterize associations between incident symptomatic infection (illness) and history of recent illness due to other viruses (within 1–7, 8–14, 15–30, 31–60, 61–90, 91–180 days), adjusted for geographic region, age, sex, daycare/school/work attendance, household size, and number of children in the household. For SARS-CoV-2, influenza, and RSV, these analyses were repeated to study incidence of infection (including asymptomatic cases).
Findings
Of 3,560 participants, 2,969 (83%) had ≥1 illness over 4,299 person-years. Adjusted hazard ratios (aHRs) in the short term (≤2 weeks) after an illness were predominantly below 1, indicating that recent viral illness was often associated with lower risk of subsequent illness with other viruses. Across age groups, recent hRV illness was associated with lower risk of hCOV, PIV, and RSV illness (aHRs 0.07–0.27). SARS-CoV-2 illness was associated with a higher short-term risk of adenovirus and PIV illness (aHRs 3.20–3.33). In children aged 6 months–4 years, recent influenza illness was associated with higher short-term risk of SARS-CoV-2 illness. Including asymptomatic infections generally attenuated these associations.
Interpretation
Some viral illnesses may alter short-term susceptibility to subsequent viral illnesses. Interactions may differ by age and symptom status.
Funding
US Centers for Disease Control and Prevention; Washington State Department of Health.
