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Weili LI, Danhua RU, Dan XIE, Jing ZHANG, Ya CHANG, Zhaoxin YANG. Correlation between Serum IL-10,CTL and EB Virus Associated Infectious Mononucleosis Complicated with Liver Damage in Children[J]. Journal of Kunming Medical University.
Citation: Weili LI, Danhua RU, Dan XIE, Jing ZHANG, Ya CHANG, Zhaoxin YANG. Correlation between Serum IL-10,CTL and EB Virus Associated Infectious Mononucleosis Complicated with Liver Damage in Children[J]. Journal of Kunming Medical University.

Correlation between Serum IL-10,CTL and EB Virus Associated Infectious Mononucleosis Complicated with Liver Damage in Children

  •   Objective   To investigate the correlation between serum interleukin-10 (IL-10), cytotoxic T lymphocytes (CTL) and Epstein Barr virus (EBV)-associated infectious mononucleosis (IM) complicated with liver damage in children.   Methods   A prospective study was conducted on 215 children with EBV-associated IM admitted to Hainan Hospital of Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Children's Hospital of Wujiang District, Suzhou and Handan First Hospital from September 2021 to May 2025. Participants were divided into complicated group (with hepatic impairment) and non-complicated group (without hepatic impairment) based on the presence or absence of concurrent hepatic impairment. Additionally, 215 healthy children during the same period were selected as the control group. Clinical data, serum IL-10 and CTL levels were compared among groups. Restricted cubic spline (RCS) analysis was used to assess the correlation between serum IL-10, CTL, and hepatic impairment in children with EBV-associated IM. Logistic regression analysis was performed to identify relevant factors affecting hepatic impairment in children with EBV-associated IM. Receiver operating characteristic (ROC) curves were used to evaluate the predictive value of serum IL-10, CTL, and their combination for hepatic impairment in children with EBV-associated IM.   Results  Pre-treatment serum IL-10 and CTL levels in children with EBV-associated IM were higher than those in the control group (P < 0.05). EBV DNA in the complicated group was higher than in the non-complicated group (P < 0.05). Pre-treatment and 3-day post-treatment IL-10 and CTL levels in the complicated group were significantly higher than in the non-complicated group, with statistical significance (P < 0.05). RCS model analysis revealed optimal fitting when the number of knots was 3, with significant likelihood ratio test (P < 0.05). Serum IL-10 demonstrated a "U"-shaped dose-response relationship with hepatic impairment in children with EBV-associated IM (P < 0.05), with a high-risk threshold of 14.90 pg/mL. CTL showed a non-linear relationship with hepatic impairment, characterized by gradual stability followed by elevation (P < 0.05), with a high-risk threshold of 46.10%. Logistic regression analysis showed that after adjusting for EBV DNA, IL-10>14.90 pg/mL and CTL>46.10% remained independent risk factors for hepatic impairment in children with EBV-associated IM (P < 0.05). ROC curve analysis showed that the AUC value of IL-10+CTL (0.850, 95%CI: 0.795-0.895) was significantly higher than the individual AUC values of either marker (P < 0.05). Pre-treatment and 3-day post-treatment IL-10 and CTL levels in children with moderate hepatic impairment were significantly higher than in those with mild impairment, with statistical significance (P < 0.05).   Conclusion  Serum IL-10 and CTL are correlated with hepatic impairment in children with EBV-associated IM, with high-risk thresholds of 14.90 pg/mL and 46.10%, respectively. Combined detection of both markers enhances the predictive value for concurrent hepatic impairment and provides clinical guidance.
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