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Updated: Jan 7, 2026

Separation of Immune Cell Subpopulations in Peripheral Blood Samples from Children with Infectious Mononucleosis
Published on: September 7, 2022
SARS-CoV-2 Infection Is Associated With an Increased Risk of Hospital-Treated Infectious Mononucleosis due to EBV:
Snieguole Vingeliene1, Huiqi Li2, Helena Backman3
1Clinical Epidemiology and Biostatistics, School of Medical Sciences, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.
COVID-19 infection, including milder cases, may increase the risk of developing Epstein-Barr virus infectious mononucleosis (EBV-IM). This suggests SARS-CoV-2 can cause lasting immune changes, potentially leading to conditions like EBV-IM.
Area of Science:
- Immunology
- Infectious Diseases
- Epidemiology
Background:
- Persistent immune dysregulation following SARS-CoV-2 infection is hypothesized to increase susceptibility to other infections.
- Epstein-Barr virus infectious mononucleosis (EBV-IM) is a common viral illness.
- The potential link between SARS-CoV-2 and subsequent EBV-IM has not been extensively studied.
Purpose of the Study:
- To investigate the association between SARS-CoV-2 infection and the subsequent diagnosis of EBV-IM.
- To determine if the severity of COVID-19 influences the risk of developing EBV-IM.
Main Methods:
- A population-based cohort study in Sweden (January 2020 - November 2022) included 9,978,860 participants aged 3-100 without prior EBV-IM diagnosis.
- Participants were categorized into: no COVID-19, SARS-CoV-2 positive PCR test only (less severe), and hospitalized COVID-19 (more severe).
- Cox regression analysis was used to estimate hazard ratios (HR) for EBV-IM, adjusting for demographic and clinical factors.
Main Results:
- The incidence rate of EBV-IM per 100,000 person-years was 4.6 (no COVID-19), 7.8 (PCR positive only), and 10.5 (hospitalized COVID-19).
- Adjusted HR for EBV-IM was 1.61 (95% CI 1.39-1.88) for SARS-CoV-2 PCR positive individuals and 5.71 (95% CI 3.33-9.79) for hospitalized COVID-19 patients, compared to those without COVID-19.
- A significant association was observed between SARS-CoV-2 infection and increased risk of EBV-IM, even in less severe cases.
Conclusions:
- SARS-CoV-2 infection is associated with a significantly increased risk of subsequent EBV-IM diagnosis.
- This association persists even with less severe acute SARS-CoV-2 infection, indicating potential immune perturbation.
- The findings suggest that COVID-19 may trigger delayed sequelae, such as EBV-IM, highlighting the broader impact on immune function.
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