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开发一种新的 HISCL 自动化 CXCL9 免疫分析。

Development of a new HISCL automated CXCL9 immunoassay.

机构信息

Research and Development Division, Sysmex R&D Centre Europe GmbH, Falkenried 88, 20251, Hamburg, Germany.

Scientific Affairs, Sysmex Corporation, 1-3-2, Murotani, Nishi-Ku, Kobe, Hyogo, 651-14 2241, Japan.

出版信息

Sci Rep. 2023 Apr 1;13(1):5342. doi: 10.1038/s41598-023-32513-8.

Abstract

C-X-C motif chemokine ligand 9 (CXCL9), a candidate biomarker, reflects type 1 (T1) inflammation pathology. Here, we report the analytical performance and clinical characteristics of a new CXCL9 reagent for a fully automated immunoassay device. We evaluated the limits of blank, detection, and quantitation (LoQ) along with other efficacy parameters, and the ability of the assay to report patient health, COVID-19 status, and the presence of asthma and/or interstitial lung diseases (ILDs). The coefficient of variation for 5-day total precision using two instruments was 7% across two controls, serum, and plasma panels. LoQ of 2.2 pg/mL suggested the efficacy of the assay in detecting T1 inflammation in plasma or serum; no cross-reactivity or interference was observed. We identified high serum CXCL9 levels in samples from patients with acute COVID-19 infections (n = 57), chronic bird-related hypersensitivity pneumonitis (n = 61), asthma (n = 194), and ILDs (n = 84) compared to healthy individuals (< 39.0 pg/mL). Furthermore, CXCL9 levels increased with age in asthma patients, and an opposite trend was observed for T2 inflammatory factors. These results suggest the utility of the automated CXCL9 immunoassay for measuring CXCL9 in clinical samples and reflect its role in T1 inflammation.

摘要

C-X-C 基序趋化因子配体 9(CXCL9)是一种候选生物标志物,反映 1 型(T1)炎症病理学。在这里,我们报告了一种用于全自动免疫分析设备的新型 CXCL9 试剂的分析性能和临床特征。我们评估了空白、检测和定量(LoQ)以及其他功效参数的限值,以及该测定法报告患者健康状况、COVID-19 状态以及哮喘和/或间质性肺疾病(ILDs)存在的能力。使用两台仪器进行 5 天总精密度的变异系数在两个对照品、血清和血浆组中为 7%。2.2 pg/mL 的 LoQ 表明该测定法在检测血浆或血清中的 T1 炎症方面的功效;未观察到交叉反应或干扰。与健康个体(<39.0 pg/mL)相比,我们在患有急性 COVID-19 感染(n=57)、慢性与鸟类相关的过敏性肺炎(n=61)、哮喘(n=194)和 ILD(n=84)的患者样本中发现了高水平的血清 CXCL9。此外,在哮喘患者中,CXCL9 水平随年龄增加而增加,而 T2 炎症因子则呈现相反的趋势。这些结果表明,自动化 CXCL9 免疫分析在测量临床样本中的 CXCL9 方面具有实用性,并反映了其在 T1 炎症中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9561/10067825/2576e98d2c99/41598_2023_32513_Fig1_HTML.jpg

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