Association between HLA-DR Expression and Multidrug-resistant Infection in Patients with Severe Acute Pancreatitis

被引:11
|
作者
Yu, Zhu-xi [1 ]
Chen, Xian-cheng [1 ]
Zhang, Bei-yuan [1 ]
Liu, Ning [1 ]
Gu, Qin [1 ]
机构
[1] Nanjing Univ, Sch Med, Drum Tower Hosp, Dept Crit Care Med, Nanjing 210008, Peoples R China
基金
中国国家自然科学基金;
关键词
severe acute pancreatitis (SAP); immunomonitoring; human leukocyte antigenantigen D-related (HLA-DR); multidrug-resistant infection; SECONDARY INFECTION; RISK-FACTORS; MORTALITY; MONOCYTES;
D O I
10.1007/s11596-018-1899-9
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Multidrug-resistant (MDR) bacterial infection is a common complication of severe acute pancreatitis (SAP). This study aimed to explore the association between human leukocyte antigen-antigen D-related (HLA-DR) expression and multidrug-resistant infection in patients with SAP. A total of 24 SAP patients who were admitted to Nanjing Drum Tower Hospital between May 2015 and December 2016 were enrolled in the study. The percentages of CD4+, CD8+, natural killer (NK), and HLA-DR (CD14+) cells and the CD4+/CD8+ cell ratio on days 1,7,14, and 28 after admission were determined by flow cytometry. Eighteen patients presented with the symptoms of infection. Among them, 55.6% patients (10/18) developed MDR infection. The most common causative MDR organisms were Enterobacter cloacae and Acinetobacter baumannii. The CD4+/CD8+ cell ratio and the percentage of NK cells were similar between patients with non-MDR and patients with MDR infections. In patients without infection, the HLA-DR percentage was maintained at a high level throughout the 28 days. Compared to the patients without any infection, the HLA-DR percentage in patients with non-MDR infection was reduced on day 1 but increased and reached similar levels on day 28. In patients with MDR infection, the HLA-DR percentage remained below normal levels at all-time points. It was concluded that persistent down-regulation of HLA-DR expression is associated with MDR bacterial infection in patients with SAP.
引用
收藏
页码:449 / 454
页数:6
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