补体激活产物C4d和终末补体复合物sC5b-9的增加与坏死性软组织感染的疾病严重程度和致命结果相关

IF 4.7 3区 医学 Q2 IMMUNOLOGY
Journal of Innate Immunity Pub Date : 2022-01-01 Epub Date: 2021-12-14 DOI:10.1159/000520496
Morten Hedetoft, Martin Bruun Madsen, Cecilie Bo Hansen, Ole Hyldegaard, Peter Garred
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引用次数: 0

摘要

在坏死性软组织感染(NSTI)中,高炎症负担是巨大的。补体系统是先天免疫反应的关键,可能是减少炎症反应的一个有希望的靶点,有可能改善临床结果。然而,在NSTI中,补体激活及其与疾病严重程度和生存的关系仍然未知。因此,我们前瞻性地招募了NSTI患者,并在入院时采血,在接下来的3天内每天采血一次。采用ELISA技术检测血浆C4c、C4d、C3bc、C3dg及末端补体复合体(TCC)。共纳入242例患者,中位年龄62岁,男性占60%。全因30天死亡率为17%(95%可信区间[CI] 13-23),随访率>98%。C4c、C3dg与简化急性生理评分II呈负相关(Rho -0.22, p < 0.001, Rho -0.17, p = 0.01)。感染性休克患者(n = 114,47 %)的基线TCC水平高于非休克患者(18比14,p < 0.001)。TCC与序贯器官衰竭评估(SOFA)评分相关(Rho 0.19, p = 0.004)。在多因素Cox回归分析(调整年龄、性别、合并症和SOFA评分)中,高基线C4d (>20 ng/mL)和高C4d和TCC(>31任意单位/mL)合并与30天死亡率增加相关(风险比[HR] 3.26, 95% CI 1.56-6.81, HR 5.12, 95% CI 2.15-12.23)。高水平的C4d和TCC均为负预测值0.87。总之,我们发现在NSTI患者中,补体激活与疾病的严重程度相关。高基线C4d和高C4d合并TCC与30天死亡率增加相关。基线C4d或TCC越低,生存率越高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Increase in the Complement Activation Product C4d and the Terminal Complement Complex sC5b-9 Is Associated with Disease Severity and a Fatal Outcome in Necrotizing Soft-Tissue Infection.

Increase in the Complement Activation Product C4d and the Terminal Complement Complex sC5b-9 Is Associated with Disease Severity and a Fatal Outcome in Necrotizing Soft-Tissue Infection.

Increase in the Complement Activation Product C4d and the Terminal Complement Complex sC5b-9 Is Associated with Disease Severity and a Fatal Outcome in Necrotizing Soft-Tissue Infection.

Increase in the Complement Activation Product C4d and the Terminal Complement Complex sC5b-9 Is Associated with Disease Severity and a Fatal Outcome in Necrotizing Soft-Tissue Infection.

The hyperinflammatory burden is immense in necrotizing soft-tissue infection (NSTI). The complement system is a key during the innate immune response and may be a promising target to reduce the inflammatory response, potentially improving the clinical outcome. However, complement activation and its association to disease severity and survival remain unknown in NSTI. Therefore, we prospectively enrolled patients with NSTI and sampled blood at admission and once daily for the following 3 days. Plasma C4c, C4d, C3bc, and C3dg and the terminal complement complex (TCC) were evaluated using ELISA techniques. In total, 242 patients were included with a median age of 62 years, with a 60% male predominance. All-cause 30-day mortality was 17% (95% confidence interval [CI] 13-23) with a follow-up of >98%. C4c and C3dg were negatively correlated with Simplified Acute Physiology Score II (Rho -0.22, p < 0.001 and Rho -0.17, p = 0.01). Patients with septic shock (n = 114, 47%) had higher levels of baseline TCC than those in non-shock patients (18 vs. 14, p < 0.001). TCC correlated with the Sequential Organ Failure Assessment (SOFA) score (Rho 0.19, p = 0.004). In multivariate Cox regression analysis (adjusted for age, sex, comorbidity, and SOFA score), high baseline C4d (>20 ng/mL) and the combination of high C4d and TCC (>31 arbitrary units/mL) were associated with increased 30-day mortality (hazard ratio [HR] 3.26, 95% CI 1.56-6.81 and HR 5.12, 95% CI 2.15-12.23, respectively). High levels of both C4d and TCC demonstrated a negative predictive value of 0.87. In conclusion, we found that in patients with NSTI, complement activation correlated with the severity of the disease. High baseline C4d and combination of high C4d and TCC are associated with increased 30-day mortality. Low baseline C4d or TCC indicates a higher probability of survival.

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来源期刊
Journal of Innate Immunity
Journal of Innate Immunity 医学-免疫学
CiteScore
10.50
自引率
1.90%
发文量
35
审稿时长
7.5 months
期刊介绍: The ''Journal of Innate Immunity'' is a bimonthly journal covering all aspects within the area of innate immunity, including evolution of the immune system, molecular biology of cells involved in innate immunity, pattern recognition and signals of ‘danger’, microbial corruption, host response and inflammation, mucosal immunity, complement and coagulation, sepsis and septic shock, molecular genomics, and development of immunotherapies. The journal publishes original research articles, short communications, reviews, commentaries and letters to the editors. In addition to regular papers, some issues feature a special section with a thematic focus.
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