Abstract

Pulmonary hypertension (PH) is a frequent complication in patients with pulmonary fibrosis (PF), whereas the mechanism was not well-understood. This study aimed to explore the influence of immune cell infiltration on PH status based on the genomic expression profiles. Microarray data of GSE24988 were downloaded from the GEO database, including 116 lung tissue samples derived from PF patients with various PH status. Proportion of infiltrated immune cells was evaluated using CIBERSORT, a gene expression-based de-convolution algorithm. A random forest classifier was constructed and out of bag (OOB) cross-validation was carried out for PH prediction. The proportions of immune infiltration cells varied differently in PH samples except T regulatory cells (p-value = 0). Compared with non-PH samples, increased number of naive B cells and plasma cells were identified in PH samples, whereas activated dendritic cells and M2 macrophages were relatively lower (p < 0.05). In the random forest model, these four types of immune cells obtained a higher variable importance score than other cells, including mean decreased accuracy and mean decreased gini evaluation. We ran the OOB cross-validation in each sample of datasets (training set and testing set) and obtained 79 and 69% accuracy, respectively. Abnormal proportions of four types of immune cells were identified in PH samples compared with non-PH samples, suggesting their involvement in PH development. In summary, the immune cell infiltration in PF patients is associated with the PH status of patients, which deserves further investigation in the future.

Highlights

  • Pulmonary hypertension (PH) is a frequent complication in patients with chronic lung diseases such as idiopathic pulmonary fibrosis (IPF) and chronic obstructive pulmonary disease (COPD)

  • The p-values derived from CIBERSORT were

  • Hierarchical cluster analysis was performed on 116 samples based on these infiltrating immune cells, which suggested that individuals with PH status could not be divided from patients without PH diseases based on infiltrating immune cells status (Figure 1B)

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Summary

Introduction

Pulmonary hypertension (PH) is a frequent complication in patients with chronic lung diseases such as idiopathic pulmonary fibrosis (IPF) and chronic obstructive pulmonary disease (COPD). The presence of PH is strongly correlated with high mortality of chronic lung diseases. The pathogenesis of PH is initiated by formation of scars in lung tissues and severe vascular remodeling, causing pressure to smallest arteries and increasing resistance to blood flow [3]. Unlike systemic hypertension, this condition only affects the arteries of lungs. Many studies have been conducted for understanding this disease, patients suffered from PH-associated lung disease carrying poor prognosis. More effort aiming at PH treatment should be carried out to decrease the mortality due to chronic lung diseases

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