State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, National Clinical Research Center for Infectious Diseases, Zhejiang University School of Medicine, Hangzhou, China.
Intensive Care Unit, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Ann Clin Microbiol Antimicrob. 2024 Aug 24;23(1):79. doi: 10.1186/s12941-024-00739-7.
The aim of this work was to assess dynamic cytokine profiles associated with bloodstream infection (BSI) caused by Klebsiella pneumoniae (Kpn) and investigate the clinical features associated with mortality.
A total of 114 patients with positive BSI-Kpn and 12 sepsis individuals without blood positive bacteria culture were followed up. Cytokine profiles were analyzed by multiplex immunoassay on the first, third, seventh and fourteenth day after diagnosis. The test cytokines included arginase, interferon-gamma (IFN-γ), tumor necrosis factor alpha (TNF-α), interleukin (IL)-1β, IL-4, IL-6, IL-10, IL-12 (p70), and IL-23. The minimum inhibitory concentration (MIC) of 24 antibiotics were tested for BSI-Kpn. Risk factors associated with the 30-day mortality and 120-day mortality were evaluated using logistic analyses and nomogram.
There were 55 out of 114 patients with BSI-Kpn were included. All isolates showed high susceptibility rate to novel avibactam combinations. The level of arginase was the highest in carbapenem-resistant Kpn (CRKP) patients. The AUCs of arginase, TNF-α and IL-4 reached 0.726, 0.495, and 0.549, respectively, whereas the AUC for the combination of these three cytokines was 0.805. Notably, 120-day mortality in patients with CRKP was higher than carbapenem-sensitive K. pneumoniae (CSKP). Furthermore, the long-term and high levels of IL-6 and IL-10 were associated with death.
High expression of arginase is correlated with CRKP. In addition, BSI-CRKP could result in indolent clinic course but poor long-term prognosis. Continuous increase of IL-6 and IL-10 were associated with mortality.
本研究旨在评估与肺炎克雷伯菌(Kpn)引起的血流感染(BSI)相关的动态细胞因子谱,并探讨与死亡率相关的临床特征。
对 114 例 BSI-Kpn 阳性患者和 12 例血培养无阳性细菌的败血症患者进行随访。在诊断后的第 1、3、7 和 14 天,通过多重免疫分析法分析细胞因子谱。检测的细胞因子包括精氨酸酶、干扰素-γ(IFN-γ)、肿瘤坏死因子-α(TNF-α)、白细胞介素(IL)-1β、IL-4、IL-6、IL-10、IL-12(p70)和 IL-23。对 BSI-Kpn 进行了 24 种抗生素的最小抑菌浓度(MIC)检测。采用逻辑分析和列线图评估与 30 天死亡率和 120 天死亡率相关的危险因素。
在 114 例 BSI-Kpn 患者中,有 55 例被纳入研究。所有分离株对新型头孢他啶-阿维巴坦组合均显示出高敏感性。碳青霉烯耐药肺炎克雷伯菌(CRKP)患者精氨酸酶水平最高。精氨酸酶、TNF-α和 IL-4 的 AUC 分别达到 0.726、0.495 和 0.549,而这三种细胞因子的组合 AUC 为 0.805。值得注意的是,CRKP 患者的 120 天死亡率高于碳青霉烯敏感肺炎克雷伯菌(CSKP)。此外,长期和高水平的 IL-6 和 IL-10 与死亡相关。
精氨酸酶的高表达与 CRKP 相关。此外,BSI-CRKP 可能导致慢性临床过程,但预后较差。IL-6 和 IL-10 的持续增加与死亡率相关。