Attenuated interferon-γ following injury is associated with chronic critical illness.

IF 2.9 2区 医学 Q2 CRITICAL CARE MEDICINE
Joseph Cuschieri, Lucy Z Kornblith, Hashem Kalthoum, Sophia Cuschieri, Shibani Pati, Adrian Piliponsky
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引用次数: 0

Abstract

Objective: Altered genomic expression of interferon (IFN)-γ has been demonstrated to be associated with the development of organ failure following severe injury. Altered expression of IFN-γ on innate immunity and long-term outcomes have not been previously examined. The purpose of this study was to determine the effect that IFN-γ plays on monocyte function and development of chronic critical illness (CCI).

Methods: Severely injured patients were prospectively evaluated in a development cohort (n = 124). Blood was drawn within 12 hours of injury. Plasma IFN-γ was determined by immune-assay. Clinical and outcome data were prospectively obtained for 1 year. Within this development cohort, a plasma IFN-γ level associated with CCI was determined. This IFN-γ level was analyzed within a separate prospective validation cohort (n = 78). Blood samples in this validation cohort underwent analysis for monocyte activation.

Results: In the development cohort, an IFN-γ ≤ 50 pg/mL was associated with the development of CCI. This IFN-γ level was independently associated with CCI in the developmental cohort after adjusting for age, Injury Severity Score, lactate concentration, and blood transfusions. An IFN-γ ≤ 50 pg/mL within the validation cohort was associated with a statistically significant increase in CCI, nosocomial infection, poor discharge disposition, and 1-year mortality (25% vs. 4%, p = 0.005). Consistent with the development of CCI, attenuated IFN-γ was associated with decreased monocyte activation and surface human leukocyte antigen-DR expression.

Conclusion: Decreased IFN-γ is predictive of CCI development. This reduction in IFN-γ is associated with a reduction in human leukocyte antigen-DR and monocyte activation, which may result in the development of CCI, increased nosocomial infections, and poor long-term outcomes. Interferon-γ levels early following injury may be useful as a biomarker for prognosis and to serve to identify patients who could benefit from IFN-γ administration or other novel therapeutic interventions to prevent long-term complications.

Level of evidence: Prognostic and Epidemiological; Level III.

损伤后干扰素γ衰减与慢性危重疾病相关。
目的:干扰素(IFN)-γ的基因组表达改变已被证明与严重损伤后器官衰竭的发展有关。IFN-γ表达的改变对先天免疫和长期结果的影响此前尚未得到研究。本研究的目的是确定IFN-γ对单核细胞功能和慢性危重症(CCI)发展的影响。方法:对124例严重损伤患者进行前瞻性研究。受伤后12小时内抽血。免疫法测定血浆IFN-γ。前瞻性地获得了1年的临床和结局数据。在这个发展队列中,血浆IFN-γ水平与CCI相关。IFN-γ水平在单独的前瞻性验证队列中进行分析(n = 78)。该验证队列的血液样本进行了单核细胞活化分析。结果:在发展队列中,IFN-γ≤50 pg/mL与CCI的发展相关。在调整年龄、损伤严重程度评分、乳酸浓度和输血后,发育队列中IFN-γ水平与CCI独立相关。验证队列中IFN-γ≤50 pg/mL与CCI、医院感染、出院处置不良和1年死亡率的统计学显著增加相关(25% vs. 4%, p = 0.005)。与CCI的发展一致,减弱的IFN-γ与单核细胞活化和表面人白细胞抗原- dr表达降低有关。结论:IFN-γ降低可预测CCI的发展。IFN-γ的减少与人类白细胞抗原dr和单核细胞活化的减少有关,这可能导致CCI的发展,增加医院感染和不良的长期预后。损伤后早期干扰素-γ水平可作为预后的生物标志物,并可用于识别可从干扰素-γ给药或其他新型治疗干预措施中获益的患者,以预防长期并发症。证据水平:预后和流行病学;第三层次。
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来源期刊
CiteScore
6.00
自引率
11.80%
发文量
637
审稿时长
2.7 months
期刊介绍: The Journal of Trauma and Acute Care Surgery® is designed to provide the scientific basis to optimize care of the severely injured and critically ill surgical patient. Thus, the Journal has a high priority for basic and translation research to fulfill this objectives. Additionally, the Journal is enthusiastic to publish randomized prospective clinical studies to establish care predicated on a mechanistic foundation. Finally, the Journal is seeking systematic reviews, guidelines and algorithms that incorporate the best evidence available.
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