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Separation of Immune Cell Subpopulations in Peripheral Blood Samples from Children with Infectious Mononucleosis
Published on: September 7, 2022
Association between Epstein-Barr viral load and duration of hospitalization in pediatric infectious mononucleosis: a
Zhi Yang1, Zongtao Ma2, Qingfeng Fang1
1Department of Pediatric Infectious Disease, Anhui Provincial Children's Hospital, Hefei, China.
Insights
High Epstein-Barr virus (EBV) DNA load in children indicates more severe illness, including liver injury and complications, leading to longer hospital stays. Monitoring EBV viral load can help identify at-risk children early.
Area of Science:
- Pediatric Infectious Diseases
- Virology
- Clinical Medicine
Background:
- Epstein-Barr virus (EBV) infection presents diverse clinical outcomes in children, from mild to severe. The impact of EBV DNA load on disease severity and progression is not fully understood.
- Understanding EBV's clinical heterogeneity is crucial for effective pediatric management.
Purpose of the Study:
- To determine the correlation between Epstein-Barr virus (EBV) DNA load and clinical features, treatment outcomes, and prognosis in pediatric patients.
- To assess the role of EBV viral load in disease severity and hospitalization duration.
Main Methods:
- A cohort of 192 children with EBV infection was analyzed, stratified into high (n=99) and low (n=93) EBV DNA load groups.
- Clinical data, treatment, viral dynamics, complications, and hospitalization length were compared between groups.
- Multivariate Cox regression identified factors influencing hospitalization duration.
Main Results:
- The high EBV DNA load group showed significantly higher peak ALT, AST, and atypical lymphocytes, with more frequent glucocorticoid use and prolonged hospitalization (p<0.001).
- Higher incidence of overall complications (p<0.001) and splenomegaly (p=0.001) were observed in the high viral load group.
- High viral load (HR=0.528) and splenomegaly (HR=0.665) independently predicted longer hospital stays.
Conclusions:
- Elevated EBV DNA load in children is linked to severe hepatic injury, increased complications, and extended hospitalization.
- Viral load monitoring is valuable for early risk stratification and predicting unfavorable outcomes in pediatric EBV infections.
Background:
Epstein-Barr virus (EBV) infection exhibits considerable heterogeneity in clinical manifestations among children, ranging from self-limiting symptoms to severe complications. The role of viral load in disease progression remains incompletely understood.
Objective:
To investigate the relationship between EBV DNA load levels and clinical characteristics, treatment response, and prognosis in pediatric patients.
Methods:
A total of 192 children diagnosed with EBV infection and admitted to our hospital between January 2022 and October 2025 were included in the final analysis. Based on plasma EBV DNA levels at admission, patients were stratified into a high viral load group (n = 99) and a low viral load group (n = 93). Baseline clinical data, treatment regimens, virological and serological dynamics, incidence of complications, and length of hospital stay were collected and compared between the two groups. A multivariate Cox proportional hazards regression model was employed to identify independent factors influencing hospitalization duration.
Results:
Comparative analysis of baseline characteristics revealed that the high viral load group exhibited significantly elevated peak alanine aminotransferase (ALT) (p < 0.001), peak aspartate aminotransferase (AST) (p < 0.001), and proportion of atypical lymphocytes (p = 0.036) relative to the low viral load group. Regarding treatment, glucocorticoid administration was more frequent in the high viral load group (p = 0.002), and the duration of hospitalization was prolonged (p < 0.001). Virologically, EBV DNA levels were higher in the high viral load group both at admission (all p < 0.001), with significant reduction observed in both groups by discharge (all p < 0.001). The incidence of overall complications (p < 0.001) and splenomegaly (p = 0.001) was greater in the high viral load group. Multivariate Cox regression analysis, with hospitalization duration as the dependent variable, identified high viral load (HR = 0.528, p < 0.001) and splenomegaly (HR = 0.665, p = 0.016) as independent predictors of prolonged hospital stay.
Conclusion:
High EBV DNA load is independently associated with more severe hepatic injury, increased risk of complications, greater need for immunomodulatory therapy, and extended hospitalization. Viral load monitoring may facilitate early identification of children at high risk of unfavorable clinical outcomes.
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