
SARS-CoV-2 co-infection with influenza virus, respiratory syncytial virus or adenovirus
,
As many countries reduce the use of such measures,
we expect SARS-CoV-2 to circulate with other respiratory viruses, increasing the likelihood of concomitant infections.
,
The clinical outcome of respiratory viral co-infections with SARS-CoV-2 is unknown.
Details on patient recruitment, inclusion criteria, testing and statistical analyzes are included in appendix (pp. 2-3). Ethical approval was given by the South Central-Oxford C Research Ethics Committee in England (13 / SC / 0149), Scotland A Research Ethics Committee (20 / SS / 0028) and the WHO Ethics Review Committee (RPC571 and RPC572, April, 2013).
TableMultivariate model of the effect of co-infection compared to SARS-CoV-2 monoinfection
The model is adjusted for the following confounders: age, gender, number of comorbidities, treatment with corticosteroids, days since the onset of the pandemic, co-infection, and 4C Mortality Score. OR = odds ratio.
This study had several strengths. First, it is the largest study of people with COVID-19 undergoing further testing for endemic respiratory viruses, reporting 583 confirmed co-infections and 6382 confirmed SARS-CoV-2 monoinfections. Second, we recruited patients over a duration of 18 months. Finally, we report outcome data for most patients.
we assume that viral co-infection was present at the time of hospitalization in most study patients. Finally, because influenza virus vaccination data were not recorded in the database and since most patients were admitted before COVID-19 vaccinations were available, we were unable to determine the effect of influenza virus or SARS-CoV-2 vaccination on the outcome in monoinfected and co-infected patients.
As public health restrictions are lifted, respiratory virus co-infections are more likely to occur in future winters. The marked increase in risk among patients with concomitant infection has several implications for the policy. First, our results provide further support for vaccination against both SARS-CoV-2 and influenza virus. Second, they suggest that testing for influenza virus is important in hospitalized patients with COVID-19 to identify patients at risk and a cohort of patients who may have different responses to immunomodulatory and antiviral therapy.
All authors declare support from the National Institute for Health Research (NIHR), Medical Research Council (MRC), NIHR Health Protection Unit (HPRU) in Emerging and Zoonotic Infections at the University of Liverpool, NIHR HPRU in Respiratory Infections at Imperial College London, NIHR Biomedical Research Center at Imperial College London and the NIHR Clinical Research Network. JKB and ABD report on grants from the UK Department of Health and Social Care (DHSC) during the conduct of the study and grants from the Wellcome Trust. PJMO reports personal fees from consulting firms (ie GlaxoSmithKline, Janssen, Bavarian Nordic, Pfizer and Cepheid) and for the European Respiratory Society; grants from MRC, MRC Global Challenge Research Fund, EU, NIHR Biomedical Research Center, MRC – GlaxoSmithKline, Wellcome Trust and NIHR (HPRU in Respiratory Infection); and is an NIHR senior investigator, not related to this correspondence. PJMO’s role as president of the British Society for Immunology was unpaid, but travel and accommodation at some meetings were paid for by the company. JKB reports grants from MRC. MGS reports grants from DHSC, NIHR UK, MRC, HPRU in Emerging and Zoonotic Infections and the University of Liverpool during the course of the study and is chair of the Scientific Advisory Committee and a minority shareholder in Integrum Scientific, unrelated to this Correspondence. GHG, MGS and JKB contributed equally. ISARIC4C investigators are listed in the appendix.
Supplementary material
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Published: March 25, 2022
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