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Xiaowei LI, Kai YANG, Fanrong WANG, Xu LIU. Evaluative Value of Serum TNFSF14,TLR7,and sCD14-ST Levels in Assessing Disease Severity and Prognosis of Respiratory Syncytial Virus Infection-Related Pneumonia in Children[J]. Journal of Kunming Medical University.
Citation: Xiaowei LI, Kai YANG, Fanrong WANG, Xu LIU. Evaluative Value of Serum TNFSF14,TLR7,and sCD14-ST Levels in Assessing Disease Severity and Prognosis of Respiratory Syncytial Virus Infection-Related Pneumonia in Children[J]. Journal of Kunming Medical University.

Evaluative Value of Serum TNFSF14,TLR7,and sCD14-ST Levels in Assessing Disease Severity and Prognosis of Respiratory Syncytial Virus Infection-Related Pneumonia in Children

  • Received Date: 2025-09-03
  •   Objective  To investigate the significance of serum tumor necrosis factor superfamily member 14 (TNFSF14), toll-like receptor 7 (TLR7), and soluble cluster of differentiation 14 subtype (sCD14-ST) levels in evaluating disease severity and prognosis in children with pneumonia associated with respiratory syncytial virus (RSV) infection.   Methods  A total of 154 children with RSV infection-related pneumonia admitted between July 2024 and July 2025 were enrolled as the disease group, classified into mild group (n = 52) and severe group (n = 102) based on disease severity. Simultaneously, 154 healthy children who underwent routine physical examinations at our hospital served as the control group. Serum levels of TNFSF14, TLR7, and sCD14-ST were measured using ELISA. According to prognosis, patients were divided into poor prognosis group (n = 35) and good prognosis group (n = 119). ROC curve analysis was performed to evaluate the value of serum TNFSF14, TLR7, and sCD14-ST levels in assessing disease severity and prognosis in children with RSV infection-related pneumonia. Multivariate Logistic regression analysis was used to identify independent factors affecting poor prognosis.   Results  Serum levels of TNFSF14, TLR7, and sCD14-ST in the disease group were significantly higher than in the control group (P < 0.05). Compared with the mild group, children in the severe group showed significantly elevated serum levels of TNFSF14, TLR7, and sCD14-ST (P < 0.05). Spearman rank correlation analysis demonstrated that serum levels of TNFSF14, TLR7, and sCD14-ST showed significant positive correlations with chest X-ray (CXR) lesion extent grade at admission (all P <0.001), with TNFSF14 showing the strongest correlation (rs = 0.484) followed by TLR7 (rs = 0.421) and sCD14-ST (rs = 0.349). Stratified analysis showed that in the severe group, the correlations between all three markers and lesion extent grade (TNFSF14: rs = 0.525, TLR7: rs = 0.493, sCD14-ST: rs = 0.424; All P <0.001) were significantly stronger than in the mild group (TNFSF14: rs = 0.31, TLR7: rs = 0.27, sCD14-ST: rs = 0.24; all P <0.05). Compared with single marker detection, combined measurement of serum TNFSF14 (Z = 4.884, P < 0.001), TLR7 (Z = 2.792, P = 0.003), and sCD14-ST (Z = 4.803, P < 0.001) levels had a higher evaluation value for disease severity in children with RSV infection-related pneumonia. Significant differences were observed between the poor and good prognosis groups in lesion extent grade, lesion type, and presence of complications (P < 0.05). Compared with the good prognosis group, the poor prognosis group showed significantly elevated serum levels of TNFSF14, TLR7, and sCD14-ST (P < 0.05). Compared with individual detection, the combined detection of serum TNFSF14 (Z = 3.902, P < 0.001), TLR7 (Z = 3.434, P < 0.001), and sCD14-ST (Z = 2.394, P = 0.017) levels had a higher prognostic value for children with RSV pneumonia. Multivariate logistic regression analysis revealed that serum levels of TNFSF14 (OR = 4.351), TLR7 (OR = 2.635), sCD14-ST (OR = 1.695), diffuse infiltration (OR = 4.121), and presence of complications (OR = 3.570) were independent factors affecting poor prognosis in children with RSV infection-related pneumonia (P < 0.05).   Conclusion  Serum levels of TNFSF14, TLR7, and sCD14-ST are significantly elevated in children with RSV infection-related pneumonia. Combined detection of these three markers enhances the evaluation value for assessing disease severity and prognosis.
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