间接免疫荧光法测定职业性细菌抗原抗体滴度的自动图像分析。

P. Brauner, U. Jäckel
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引用次数: 2

摘要

接触高浓度生物气溶胶中的微生物的员工经常患呼吸系统疾病。然而,病因学,特别是微生物在发病机制中的潜在作用仍然需要阐明。因此,测定员工针对特定职业微生物抗原的抗体滴度可能导致潜在有害物种的鉴定。由于间接免疫荧光(IIF)易于实现,我们使用该技术分析人血清中的免疫反应。为了解决不利的观察者之间的变化,以及在传统的眼睛滴度测定中缺乏可量化的荧光数据,我们专门开发了一个自动图像分析的软件工具。“荧光分析仪”软件能够可靠地量化数字图像上抗体结合细菌细胞的荧光强度。随后,使用单细胞的荧光值计算非离散IgG滴度。我们在20名志愿者的血清中测试了这种方法,并检测了多种工作场所细菌分离株的滴度。此外,我们将基于图像的结果与传统的手动读数进行了比较,发现了显著的相关性和统计学上证实的可重复性。总之,我们成功地使用了“Fluorolyzer”来测定针对各种细菌的滴度,并证明了它作为可靠和有效分析职业暴露于生物气溶胶的免疫反应的有用工具的适用性。
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Automated Image Analysis for Determination of Antibody Titers Against Occupational Bacterial Antigens Using Indirect Immunofluorescence.
Employees who are exposed to high concentrations of microorganisms in bioaerosols frequently suffer from respiratory disorders. However, etiology and in particular potential roles of microorganisms in pathogenesis still need to be elucidated. Thus, determination of employees' antibody titers against specific occupational microbial antigens may lead to identification of potentially harmful species. Since indirect immunofluorescence (IIF) is easy to implement, we used this technique to analyze immunoreactions in human sera. In order to address disadvantageous inter-observer variations as well as the absence of quantifiable fluorescence data in conventional titer determination by eye, we specifically developed a software tool for automated image analysis. The 'Fluorolyzer' software is able to reliably quantify fluorescence intensities of antibody-bound bacterial cells on digital images. Subsequently, fluorescence values of single cells have been used to calculate non-discrete IgG titers. We tested this approach on multiple bacterial workplace isolates and determined titers in sera from 20 volunteers. Furthermore, we compared image-based results with the conventional manual readout and found significant correlation as well as statistically confirmed reproducibility. In conclusion, we successfully employed 'Fluorolyzer' for determination of titers against various bacterial species and demonstrated its applicability as a useful tool for reliable and efficient analysis of immune response toward occupational exposure to bioaerosols.
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