Assessing sepsis-induced immunosuppression to predict positive blood cultures.

IF 5.7 2区 医学 Q1 IMMUNOLOGY
Frontiers in Immunology Pub Date : 2024-11-04 eCollection Date: 2024-01-01 DOI:10.3389/fimmu.2024.1447523
Enrique Hernández-Jiménez, Erika P Plata-Menchaca, Damaris Berbel, Guillem López de Egea, Macarena Dastis-Arias, Laura García-Tejada, Fabrizio Sbraga, Pierre Malchair, Nadia García Muñoz, Alejandra Larrad Blasco, Eva Molina Ramírez, Xose Pérez Fernández, Joan Sabater Riera, Arnau Ulsamer
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引用次数: 0

Abstract

Introduction: Bacteremia is a life-threatening condition that can progress to sepsis and septic shock, leading to significant mortality in the emergency department (ED). The standard diagnostic method, blood culture, is time-consuming and prone to false positives and false negatives. Although not widely accepted, several clinical and artificial intelligence-based algorithms have been recently developed to predict bacteremia. However, these strategies require further identification of new variables to improve their diagnostic accuracy. This study proposes a novel strategy to predict positive blood cultures by assessing sepsis-induced immunosuppression status through endotoxin tolerance assessment.

Methods: Optimal assay conditions have been explored and tested in sepsis-suspected patients meeting the Sepsis-3 criteria. Blood samples were collected at ED admission, and endotoxin (lipopolysaccharide, LPS) challenge was performed to evaluate the innate immune response through cytokine profiling.

Results: Clinical variables, immune cell population biomarkers, and cytokine levels (tumor necrosis factor [TNFα], IL-1β, IL-6, IL-8, and IL-10) were measured. Patients with positive blood cultures exhibited significantly lower TNFα production after LPS challenge than did those with negative blood cultures. The study also included a validation cohort to confirm that the response was consistent.

Discussion: The results of this study highlight the innate immune system immunosuppression state as a critical parameter for sepsis diagnosis. Notably, the present study identified a reduction in monocyte populations and specific cytokine profiles as potential predictive markers. This study showed that the LPS challenge can be used to effectively distinguish between patients with bloodstream infection leading to sepsis and those whose blood cultures are negative, providinga rapid and reliable diagnostic tool to predict positive blood cultures. The potential applicability of these findings could enhance clinical practice in terms of the accuracy and promptness of sepsis diagnosis in the ED, improving patient outcomes through timely and appropriate treatment.

评估败血症引起的免疫抑制,预测血培养阳性。
导言:菌血症是一种危及生命的疾病,可发展为败血症和脓毒性休克,导致急诊科(ED)患者大量死亡。标准诊断方法是血液培养,这种方法耗时长,而且容易出现假阳性和假阴性。尽管尚未被广泛接受,但最近已开发出几种基于临床和人工智能的算法来预测菌血症。然而,这些策略需要进一步确定新的变量,以提高其诊断准确性。本研究提出了一种通过内毒素耐受性评估脓毒症诱导的免疫抑制状态来预测血培养阳性的新策略:方法:在符合败血症-3 标准的败血症疑似患者中探索并测试了最佳检测条件。在急诊室入院时采集血液样本,进行内毒素(脂多糖,LPS)挑战,通过细胞因子谱分析评估先天性免疫反应:结果:测量了临床变量、免疫细胞群生物标志物和细胞因子水平(肿瘤坏死因子[TNFα]、IL-1β、IL-6、IL-8 和 IL-10)。血液培养呈阳性的患者在接受 LPS 挑战后,TNFα 的产生量明显低于血液培养呈阴性的患者。该研究还包括一个验证队列,以确认反应是一致的:讨论:本研究结果强调了先天性免疫系统免疫抑制状态是脓毒症诊断的关键参数。值得注意的是,本研究发现单核细胞群和特定细胞因子谱的减少是潜在的预测标志物。本研究表明,LPS 挑战可用于有效区分导致败血症的血流感染患者和血培养阴性的患者,为预测血培养阳性提供了快速可靠的诊断工具。这些研究结果的潜在适用性可提高急诊室脓毒症诊断的准确性和及时性,通过及时和适当的治疗改善患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.80
自引率
11.00%
发文量
7153
审稿时长
14 weeks
期刊介绍: Frontiers in Immunology is a leading journal in its field, publishing rigorously peer-reviewed research across basic, translational and clinical immunology. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Immunology is the official Journal of the International Union of Immunological Societies (IUIS). Encompassing the entire field of Immunology, this journal welcomes papers that investigate basic mechanisms of immune system development and function, with a particular emphasis given to the description of the clinical and immunological phenotype of human immune disorders, and on the definition of their molecular basis.
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