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本文引用的文献

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Clinical utility analysis of the Hoxb8 mast cell activation test for the diagnosis of peanut allergy.用于诊断花生过敏的Hoxb8肥大细胞活化试验的临床效用分析
Allergy. 2025 Jan;80(1):215-226. doi: 10.1111/all.16341. Epub 2024 Sep 28.
2
A Streamlined Strategy for Basophil Activation Testing in a Multicenter Phase III Clinical Trial.多中心III期临床试验中嗜碱性粒细胞激活试验的简化策略
J Allergy Clin Immunol Pract. 2024 Dec;12(12):3383-3392.e8. doi: 10.1016/j.jaip.2024.09.007. Epub 2024 Sep 14.
3
Identification of a New and Effective Marker Combination for a Standardized and Automated Bin-Based Basophil Activation Test (BAT) Analysis.鉴定用于标准化和自动化基于分箱的嗜碱性粒细胞活化试验(BAT)分析的新型有效标志物组合。
Diagnostics (Basel). 2024 Sep 4;14(17):1959. doi: 10.3390/diagnostics14171959.
4
Blood stored in EDTA tubes provides accurate peanut basophil activation test results for 48 hours.EDTA 管中储存的血液可在 48 小时内提供准确的花生嗜碱性粒细胞激活试验结果。
Ann Allergy Asthma Immunol. 2024 Oct;133(4):445-452.e5. doi: 10.1016/j.anai.2024.06.022. Epub 2024 Jul 3.
5
Basophil activation in insect venom allergy: comparison of an established test using liquid reagents with a test using 5-color tubes with dried antibody reagents.昆虫毒液过敏中的嗜碱性粒细胞激活:使用液体试剂的既定检测方法与使用带有干燥抗体制剂的五色管检测方法的比较。
BMC Immunol. 2024 Apr 27;25(1):23. doi: 10.1186/s12865-024-00616-0.
6
Flow-based basophil activation test in immediate drug hypersensitivity. An EAACI task force position paper.速发型药物超敏反应中基于流式细胞术的嗜碱性粒细胞活化试验。欧洲变态反应和临床免疫学会(EAACI)工作组立场文件
Allergy. 2024 Mar;79(3):580-600. doi: 10.1111/all.15957. Epub 2023 Dec 12.
7
Combining avidin with CD63 improves basophil activation test accuracy in classifying peanut allergy.结合亲和素与 CD63 可提高嗜碱性粒细胞激活试验对花生过敏分类的准确性。
Allergy. 2024 Feb;79(2):445-455. doi: 10.1111/all.15930. Epub 2023 Nov 2.
8
EAACI guidelines on the diagnosis of IgE-mediated food allergy.EAACI 指南:IgE 介导的食物过敏诊断。
Allergy. 2023 Dec;78(12):3057-3076. doi: 10.1111/all.15902. Epub 2023 Oct 10.
9
EAACI task force report: A consensus protocol for the basophil activation test for collaboration and external quality assurance.欧洲变态反应和临床免疫学会(EAACI)特别工作组报告:嗜碱性粒细胞活化试验协作与外部质量保证的共识方案
Allergy. 2024 Feb;79(2):290-293. doi: 10.1111/all.15907. Epub 2023 Oct 5.
10
Towards standardizing basophil identification by flow cytometry.迈向流式细胞术鉴定嗜碱性粒细胞的标准化。
Front Allergy. 2023 Mar 3;4:1133378. doi: 10.3389/falgy.2023.1133378. eCollection 2023.

一种用于简化嗜碱性粒细胞活化试验的手动微流控样品制备至分析工作流程。

A hand-operated microfluidic sample preparation-to-analysis workflow for simplifying the basophil activation test.

作者信息

Castaño Nicolas, Chua Kaiser, Nguyen An, Marshall Wyeth, Hofmann Grady H, Lee Jonathan, Tsai Mindy, Sindher Sayantani B, Nadeau Kari C, Chinthrajah R Sharon, Galli Stephen J, Tang Sindy K Y

机构信息

Department of Mechanical Engineering, Stanford University, USA.

Department of Pathology, Stanford University, USA.

出版信息

Lab Chip. 2025 Jul 23;25(15):3779-3791. doi: 10.1039/d5lc00037h.

DOI:10.1039/d5lc00037h
PMID:40600291
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12315523/
Abstract

Access to the basophil activation test (BAT) has been hindered by the requirement for fresh blood analysis, specialized laboratory equipment, and advanced technical expertise. To address these issues, we have developed a hand-operated microfluidic sample preparation "μF-prep" device to perform the most time sensitive steps of the assay and stabilize the sample, effectively extending the time window before flow cytometry analysis. The μF-prep device performs concurrent basophil stimulation and staining for eight conditions in parallel. Barcoded staining of basophils allows the pooling of all conditions into one lyse/fix buffer tube for sample stabilization. After flow cytometry analysis, an XGBoost-enabled analysis pipeline unpools the eight conditions and generates basophil counts and activation levels directly from raw flow cytometry data. To characterize the μF-prep device, we stimulate whole blood samples from peanut-allergic and non-allergic donors. We compare μF-prep with a conventional BAT sample preparation protocol ("conv-prep"), and assess the stability of stimulated samples stored in the lyse/fix buffer. The μF-prep device performs sample preparation with <2 minutes of active user engagement. Our analysis pipeline shows excellent agreement with manual gating analysis. Compared with conv-prep, μF-prep exhibits similar activation levels at peanut doses of 1-100 ng mL, maximum activation levels, area under the dose response curve, and EC values. Activation levels of basophils from anonymous and presumed non-allergic donors in samples stored in the lyse/fix buffer for up to 7 days at 4 °C are similar to those analyzed on day 0. In summary, we demonstrate the potential of μF-prep to facilitate access to the BAT by simplifying sample preparation, stabilizing samples to remove the need for overnight blood shipping for flow cytometry analysis, and automating the data analysis pipeline.

摘要

由于需要进行新鲜血液分析、使用专门的实验室设备以及具备先进的技术专长,嗜碱性粒细胞活化试验(BAT)的应用受到了限制。为了解决这些问题,我们开发了一种手动微流控样品制备“μF-prep”装置,以执行该检测中最对时间敏感的步骤并稳定样品,从而有效延长流式细胞术分析前的时间窗口。μF-prep装置可并行对八个条件同时进行嗜碱性粒细胞刺激和染色。对嗜碱性粒细胞进行条形码染色可将所有条件的样本汇集到一个裂解/固定缓冲管中以稳定样品。在进行流式细胞术分析后,一个启用XGBoost的分析流程会将八个条件解池,并直接从原始流式细胞术数据生成嗜碱性粒细胞计数和活化水平。为了表征μF-prep装置,我们刺激了来自花生过敏和非过敏供体的全血样本。我们将μF-prep与传统的BAT样品制备方案(“conv-prep”)进行比较,并评估储存在裂解/固定缓冲液中的刺激样本的稳定性。μF-prep装置在用户主动操作不到2分钟的时间内即可完成样品制备。我们的分析流程与手动设门分析显示出极佳的一致性。与conv-prep相比,在花生剂量为1-100 ng/mL时,μF-prep表现出相似的活化水平、最大活化水平、剂量反应曲线下面积和EC值。储存在裂解/固定缓冲液中的来自匿名且假定为非过敏供体的嗜碱性粒细胞样本,在4℃下保存长达7天,其活化水平与第0天分析的样本相似。总之,我们证明了μF-prep通过简化样品制备、稳定样品以消除流式细胞术分析所需的隔夜血液运输需求以及使数据分析流程自动化,从而促进BAT应用的潜力。