Department II of Respiratory Medicine, National Clinical Research Center for Respiratory Diseases, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, People's Republic of China.
Division of Pulmonology, Department of Pediatrics, Third Affiliated Hospital of Zhengzhou University, Henan, People's Republic of China.
Emerg Microbes Infect. 2024 Dec;13(1):2324078. doi: 10.1080/22221751.2024.2324078. Epub 2024 Apr 4.
Paediatric pneumonia (MPP) is a heterogeneous disease with a diverse spectrum of clinical phenotypes. No studies have demonstrated the relationship between underlying endotypes and clinical phenotypes as well as prognosis about this disease. Thus, we conducted a multicentre prospective longitudinal study on children hospitalized for MPP between June 2021 and March 2023, with the end of follow-up in August 2023. Blood samples were collected and processed at multiple time points. Multiplex cytokine assay was performed to characterize serum cytokine profiles and their dynamic changes after admission. Cluster analysis based on different clinical phenotypes was conducted. Among the included 196 patients, the levels of serum IL-17A and IL-6 showed remarkable variabilities. Four cytokine clusters based on the two cytokines and four clinical groups were identified. Significant elevation of IL-17A mainly correlated with diffuse bronchiolitis and lobar lesion by airway mucus hypersecretions, while that of IL-6 was largely associated with lobar lesion which later developed into lung necrosis. Besides, glucocorticoid therapy failed to inhibit IL-17A, and markedly elevated IL-17A and IL-6 levels may correlate with lower airway obliterans. Our study provides critical relationship between molecular signatures (endotypes) and clustered clinical phenotypes in paediatric patients with MPP.
儿童肺炎(MPP)是一种异质性疾病,具有多种临床表型。目前尚无研究表明该疾病的潜在表型与临床表型以及预后之间的关系。因此,我们于 2021 年 6 月至 2023 年 3 月期间对因 MPP 住院的儿童进行了一项多中心前瞻性纵向研究,随访于 2023 年 8 月结束。在多个时间点采集并处理血样。采用多重细胞因子检测法分析血清细胞因子谱及其入院后的动态变化。根据不同的临床表型进行聚类分析。在纳入的 196 例患儿中,血清 IL-17A 和 IL-6 水平表现出显著的变异性。根据这两种细胞因子和四个临床组确定了四个细胞因子簇。IL-17A 的显著升高主要与气道黏液高分泌引起的弥漫性细支气管炎和肺叶病变有关,而 IL-6 的升高则与后来发展为肺坏死的肺叶病变密切相关。此外,糖皮质激素治疗未能抑制 IL-17A,而明显升高的 IL-17A 和 IL-6 水平可能与小气道闭塞有关。我们的研究为 MPP 患儿的分子特征(表型)与聚类临床表型之间提供了重要的关系。