Antibody Titer Prediction from Serum Immunodiffusion Test of Patients with Paracoccidioidomycosis Using Infrared Spectroscopy and Chemometrics

Analytica Pub Date : 2023-09-06 DOI:10.3390/analytica4030028
A. Koehler, M. L. Scroferneker, Paulo Cezar de Moraes, Beatriz Aparecida Soares Pereira, R. S. Cavalcante, R. P. Mendes, V. Corbellini
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引用次数: 0

Abstract

Paracoccidioidomycosis (PCM) is a systemic mycosis caused by fungi of the genus Paracoccidioides. Serological tests are auxiliary in the diagnosis of PCM. However, the lack of standardization is a central problem in serodiagnosis and antibody titration. The objective of this study was to propose a methodology based on Fourier transform infrared spectroscopy (FTIR) for predicting antibody titers in patients with PCM. A total of 118 serum samples from patients with PCM were included, for which antibody titration using double immunodiffusion (DID) was previously performed. Serum samples were analyzed by attenuated total reflection (ATR)-FTIR and a supervised analysis with partial least squares regression (PLS) was used to predict the antibody titers. The PLS model with two latent variables and with the use of one orthogonal signal correction (OSC) showed a determination coefficient (R2) higher than 0.9999 for both the calibration and prediction set. The model was able to predict the antibody titers from patients with PCM with a minimal error. Therefore, modeling with FTIR/ATR and multivariate calibration proved to be a fast and highly accurate method for antibody titration, replacing the need for antigen production and performance of traditional serological tests.
用红外光谱和化学计量学预测副球孢子菌病患者血清免疫扩散试验的抗体滴度
副球孢子菌病(PCM)是一种由副球孢子菌属真菌引起的系统性真菌病。血清学检测是诊断PCM的辅助手段。然而,缺乏标准化是血清诊断和抗体滴定的中心问题。本研究的目的是提出一种基于傅立叶变换红外光谱(FTIR)预测PCM患者抗体滴度的方法。共纳入118份来自PCM患者的血清样本,之前使用双免疫扩散(DID)进行抗体滴定。血清样品采用衰减全反射(ATR)-FTIR分析,并采用偏最小二乘回归(PLS)的监督分析预测抗体滴度。采用单正交信号校正(OSC)的双潜变量PLS模型,校正集和预测集的决定系数(R2)均大于0.9999。该模型能够以最小的误差预测PCM患者的抗体滴度。因此,FTIR/ATR建模和多变量校准被证明是一种快速、高精度的抗体滴定方法,取代了对抗原产生和传统血清学测试性能的需要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
1.80
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0.00%
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