小儿重症肺炎病例血清中的 IL-21、IL-23 和 8-羟基-2′-脱氧鸟苷水平

N. Bayraktar, A. Güzelçi̇çek, Ali Öztürk, Mehmet Bayraktar, Hamza Erdoğdu
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摘要

背景:肺炎是大多数急性呼吸窘迫综合征(ARDS)病例的病因。引起肺炎的微生物种类繁多。除 DNA 外,RNA 病毒、革兰氏阴性菌和革兰氏阳性菌也会导致两种细胞因子失衡,即抗炎和促炎。细胞因子对败血症和其他感染性疾病的预后也有影响。本研究旨在检测 8-羟基-2'-脱氧鸟苷(8-OHdG)、IL-21、IL-23 和 c 反应蛋白(CRP),并比较细胞因子水平。这也是为了确定小儿肺炎患者的 CRP 和细胞因子水平是否与结果相关。材料和方法:在研究中,从前来儿科门诊就诊的约 43 名小儿肺炎患者和 43 名健康对照者身上抽血,以调查血清 IL-21、IL-23、8-OHdG 和 CRP 水平。生物标志物水平采用 ELISA 方法测定。使用 ATELLICA IM 分析仪测量血清 CRP 水平。结果小儿肺炎患者组的血清 CRP、8-OHdG、IL-21 和 IL-23 水平明显高于对照组。结论小儿肺炎患者血清中 IL-21、IL-23、8-OHdG 和 CRP 表达的增加是一个潜在的决定因素,表明 IL-21、IL-23 相关细胞因子可能在患者内皮细胞活化中发挥作用。8-OHdG氧化应激的增加在非小儿肺炎患者中更为明显,而在小儿肺炎患者中促炎性细胞因子则更高。然而,8-OHdG 可作为治疗目标来减轻炎症反应。还需要进一步研究这些发现对合并症的影响,并进行更大规模的测试。
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Serum Levels of IL-21, IL-23 and 8-hydroxy-2′-deoxyguanosine in Pediatric Severe Pneumonia Cases
Background: Pneumonia causes the majority of acute respiratory distress syndrome (ARDS) cases. The microbes that cause pneumonia are very diverse. In addition to DNA, RNA viruses, Gram-negative and Gram-positive bacteria cause two types of cytokine imbalances, anti-inflammatory and pro-inflammatory. It can also influence the progno-sis of sepsis and other infectious diseases. This study aims to search for 8-hydroxy-2'-deoxyguanosine (8-OHdG), IL-21, IL-23, and c-reactive protein (CRP) and compare cytokine levels. It is also to determine if Pediatric pneumonia patients CRP and cytokine levels correlate with results. Materials and Methods: In the study, blood was drawn from approximately 43 pediatric pneumonia patients and 43 healthy controls who came to the pediatric clinic to investigate serum IL-21, IL-23, 8-OHdG, and CRP levels. The levels of biomarkers were determined by ELISA method. Serum CRP levels were measured using the ATELLICA IM Analyzer. Results: Serum CRP, 8-OHdG, IL-21 and IL-23 levels were significantly higher in the pediatric pneumonia patient group than in the control group. Conclusions: Increased serum IL-21, IL-23, 8-OHdG and CRP expression in pediatric pneumonia patients is a poten-tial determinant suggesting that IL-21, IL-23-related cytokines may play a role in endothelial cell activation reported in patients. Increased 8-OHdG oxidative stress is more pronounced in patients without pediatric pneumonia while pro inflammatory cytokines are higher in pediatric pneumonia patients. However, it is used as a possible therapeu-tic target to reduce inflammation. Further study on the impact of these findings on comorbidities with larger num-ber test size is needed
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