Prediction of outcome using CD14++CD16-, CD14++CD16+ and CD14+CD16++ monocyte subpopulations in patients with complicated intra-abdominal infections.

IF 5.5 3区 医学 Q1 IMMUNOLOGY
Medical Microbiology and Immunology Pub Date : 2023-10-01 Epub Date: 2023-09-08 DOI:10.1007/s00430-023-00779-4
Evgeni Dimitrov, Krasimira Halacheva, Georgi Minkov, Emil Enchev, Yovcho Yovtchev
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引用次数: 0

Abstract

There is still no study investigating the prognostic performance of CD14++CD16-, CD14++CD16+ and CD14+CD16++ monocyte subpopulations in complicated intra-abdominal infections (cIAIs); therefore, we aimed to evaluate the association between monocyte subtypes and outcome in such patients. A single-center prospective study was conducted at a University Hospital Stara Zagora between November 2018 and August 2021. Preoperatively and on the 3rd postoperative day (POD), we measured the levels of CD14++CD16-, CD14++CD16+ and CD14+CD16++ monocytes in peripheral blood using flow cytometry in 62 patients with cIAIs and 31 healthy controls. Nine of the 62 patients died during hospitalization. Survivors had higher pre-surgery percentages of CD14++CD16- classical monocytes and higher percentage of these cells predicted favorable outcome in ROC analysis (AUROC = 0.781, p = 0.008). The CD14++CD16+ intermediate monocyte percentages were higher in non-survivors both pre- and postoperatively but only the higher preoperative values predicted a lethal outcome (AUROC = 0.722, p = 0.035). For CD14+CD16++ non-classical monocytes, non-survivors had lower percentages on day 3 post-surgery and low percentage was predictive of lethal outcome (AUROC = 0.752, p = 0.046). Perioperative levels of monocyte subpopulations in peripheral blood show a great potential for prognostication of outcome in patients with cIAIs.

Abstract Image

应用CD14++CD16-、CD14++CCD16+和CD14+CD16++单核细胞亚群预测复杂腹腔内感染患者的预后。
目前还没有研究CD14++CD16-、CD14++CCD16+和CD14+CD16++单核细胞亚群在复杂腹腔感染(cIAI)中的预后表现;因此,我们旨在评估单核细胞亚型与此类患者预后之间的关系。2018年11月至2021年8月,在Stara Zagora大学医院进行了一项单中心前瞻性研究。在术前和术后第3天(POD),我们使用流式细胞术测量了62名cAII患者和31名健康对照者外周血中CD14++CD16-、CD14++CCD16+和CD14+CD16++单核细胞的水平。62名患者中有9人在住院期间死亡。幸存者术前CD14++CD16-经典单核细胞的百分比较高,这些细胞的百分比在ROC分析中预测了良好的结果(AUROC = 0.781,p = 0.008)。CD14++CD16+中间单核细胞百分比在未存活的患者术前和术后均较高,但只有术前较高的值才能预测致死结果(AUROC = 0.722,p = 0.035)。对于CD14+CD16++非经典单核细胞,非幸存者在手术后第3天的百分比较低,低百分比可预测致死结果(AUROC = 0.752,p = 0.046)。外周血中单核细胞亚群的围手术期水平显示出预测cAIs患者预后的巨大潜力。
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来源期刊
CiteScore
10.60
自引率
0.00%
发文量
29
审稿时长
1 months
期刊介绍: Medical Microbiology and Immunology (MMIM) publishes key findings on all aspects of the interrelationship between infectious agents and the immune system of their hosts. The journal´s main focus is original research work on intrinsic, innate or adaptive immune responses to viral, bacterial, fungal and parasitic (protozoan and helminthic) infections and on the virulence of the respective infectious pathogens. MMIM covers basic, translational as well as clinical research in infectious diseases and infectious disease immunology. Basic research using cell cultures, organoid, and animal models are welcome, provided that the models have a clinical correlate and address a relevant medical question. The journal also considers manuscripts on the epidemiology of infectious diseases, including the emergence and epidemic spreading of pathogens and the development of resistance to anti-infective therapies, and on novel vaccines and other innovative measurements of prevention. The following categories of manuscripts will not be considered for publication in MMIM: submissions of preliminary work, of merely descriptive data sets without investigation of mechanisms or of limited global interest, manuscripts on existing or novel anti-infective compounds, which focus on pharmaceutical or pharmacological aspects of the drugs, manuscripts on existing or modified vaccines, unless they report on experimental or clinical efficacy studies or provide new immunological information on their mode of action, manuscripts on the diagnostics of infectious diseases, unless they offer a novel concept to solve a pending diagnostic problem, case reports or case series, unless they are embedded in a study that focuses on the anti-infectious immune response and/or on the virulence of a pathogen.
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