Abstract

In the aging process, the presence of interleukin (IL)-17-producing CD4+CD28-NKG2D+T cells (called pathogenic CD4+ T cells) is strongly associated with inflammation and the development of various diseases. Thus, their presence needs to be monitored. The emergence of attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopy empowered with machine learning is a breakthrough in the field of medical diagnostics. This study aimed to discriminate between the elderly with a low percentage (LP; ≤3%) and a high percentage (HP; ≥6%) of pathogenic CD4+CD28-NKG2D+IL17+ T cells by utilizing ATR-FTIR coupled with machine learning algorithms. ATR spectra of serum, exosome, and HDL from both groups were explored in this study. Only exosome spectra in the 1700–1500 cm−1 region exhibited possible discrimination for the LP and HP groups based on principal component analysis (PCA). Furthermore, partial least square-discriminant analysis (PLS-DA) could differentiate both groups using the 1700–1500 cm−1 region of exosome ATR spectra with 64% accuracy, 69% sensitivity, and 61% specificity. To obtain better classification performance, several spectral models were then established using advanced machine learning algorithms, including J48 decision tree, support vector machine (SVM), random forest (RF), and neural network (NN). Herein, NN was considered to be the best model with an accuracy of 100%, sensitivity of 100%, and specificity of 100% using serum spectra in the region of 1800–900 cm−1. Exosome spectra in the 1700–1500 and combined 3000–2800 and 1800–900 cm−1 regions using the NN algorithm gave the same accuracy performance of 95% with a variation in sensitivity and specificity. HDL spectra with the NN algorithm also showed excellent test performance in the 1800–900 cm−1 region with 97% accuracy, 100% sensitivity, and 95% specificity. This study demonstrates that ATR-FTIR coupled with machine learning algorithms can be used to study immunosenescence. Furthermore, this approach can possibly be applied to monitor the presence of pathogenic CD4+ T cells in the elderly. Due to the limited number of samples used in this study, it is necessary to conduct a large-scale study to obtain more robust classification models and to assess the true clinical diagnostic performance.

Highlights

  • The aging process affects the function of various organ systems as well as the immune system [1,2]

  • ATR spectra from serum, exosome, and high-density lipoprotein (HDL) samples were collected and compared in terms of biochemical contents between the low percentage (LP) and high percentage (HP) groups

  • This study explored the ATR-FTIR combined with machine learning algorithms to classify elderly subjects with different percentages of IL-17-producing CD4+CD28-NKG2D+ T

Read more

Summary

Introduction

The aging process affects the function of various organ systems as well as the immune system [1,2]. Age-related changes in the immune system, known as immunosenescence, are characterized by decreased immune responses leading to susceptibility to infectious diseases, increased expression of pro-inflammatory cytokines contributing to inflammation-related diseases, decreased vaccination response, and increased risk of autoimmune events [3–6]. Multiple age-related alterations can occur in the immune system (both innate and adaptive immune systems) [7,8]. In the adaptive immune system, age-related alterations in CD4+ T cell functions include inappropriate T helper subset differentiation, diminished proliferative capacity, and an increase in regulatory T cells [9,10]. The frequency of CD4+CD28- T cells was significantly correlated with age and, in individuals older than 65 years, the percentage of these cells could reach

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call