École du Val-De-Grâce, Service de Santé des Armées, Paris 75005, France.
Hospices Civils de Lyon, Hôpital Edouard Herriot, Laboratoire d'Immunologie, Lyon F-69003, France; EA 7426 "Pathophysiology of Injury-Induced Immunosuppression (Université Claude Bernard Lyon 1-Hospices Civils de Lyon - BioMérieux), Edouard Herriot Hospital, Lyon, France.
Cytokine. 2018 Apr;104:78-84. doi: 10.1016/j.cyto.2017.09.029. Epub 2017 Sep 30.
Functional testing protocols are thought to be the gold standard for the exploration of the immune system. However, in terms of routine analysis, they present numerous drawbacks and consequently their use is mainly limited to research applications. In the clinical context of septic shock, characterized by marked lymphocyte alterations, a new approach for lymphocyte intracellular cytokine measurement in whole blood upon was evaluated in a proof-of-concept study. Following lymphocyte activation, simultaneous intracellular labeling of Interferon-γ (IFN-γ), Tumor Necrosis Factor-α (TNF-α), and Interleukin-2 (IL-2) was performed in CD4 and CD8 T cells (identified by surface marking). The analysis was carried out by flow cytometry (6 colors). Results obtained in septic patients (n=22) were compared to those of healthy volunteers (n=8). Independently of lymphopenia, there were significant differences between groups. In particular there was significant decrease in the production of IL-2 and TNF-α in septic patients, while the production of IFN-γ was not significantly altered. Polyfunctional results showed that patients presented with increased percentages of triple negative lymphocytes. In contrast, volunteers had higher proportions of triple positive cells. The approach could be performed in a robust and consistent way, taking 4.5h to complete. Moreover, clear differences could be observed between clinical groups with this modified method. These characteristics illustrate the potential of this novel whole blood protocol for clinical applications. However, further research is required to determine the applicability compared to alternative test and to evaluate clinical performances in larger cohorts of patients.
功能测试方案被认为是探索免疫系统的金标准。然而,就常规分析而言,它们存在许多缺点,因此主要限于研究应用。在以淋巴细胞明显改变为特征的脓毒性休克的临床情况下,在概念验证研究中评估了一种新的全血淋巴细胞内细胞因子测量方法。在淋巴细胞激活后,通过流式细胞术(6 色)对 CD4 和 CD8 T 细胞(通过表面标记识别)同时进行干扰素-γ(IFN-γ)、肿瘤坏死因子-α(TNF-α)和白细胞介素-2(IL-2)的细胞内标记。在脓毒症患者(n=22)中获得的结果与健康志愿者(n=8)进行了比较。独立于淋巴细胞减少,组间存在显著差异。特别是,脓毒症患者的 IL-2 和 TNF-α产生显著减少,而 IFN-γ的产生没有显著改变。多功能结果表明,患者表现出增加的三阴性淋巴细胞百分比。相比之下,志愿者具有更高比例的三阳性细胞。该方法可以以稳健和一致的方式进行,完成需要 4.5 小时。此外,通过这种改良方法可以观察到临床组之间的明显差异。这些特征说明了这种新型全血方案在临床应用中的潜力。然而,需要进一步研究来确定与替代测试相比的适用性,并在更大的患者队列中评估临床性能。