Abstract

BackgroundRecent studies have provided evidence for an important contribution of the immune system in the pathophysiology of pulmonary arterial hypertension (PAH) and chronic thromboembolic pulmonary hypertension (CTEPH). In this report, we investigated whether the inflammatory profile of pulmonary hypertension patients changes over time and correlates with patient WHO subgroups or survival.Methods50 PAH patients (16 idiopathic (I)PAH, 24 Connective Tissue Disease (CTD)-PAH and 10 Congenital Heart Disease (CHD)-PAH), 37 CTEPH patients and 18 healthy controls (HCs) were included in the study. Plasma inflammatory markers at baseline and after 1-year follow-up were measured using ELISAs. Subsequently, correlations with hemodynamic parameters and survival were explored and data sets were subjected to unbiased multivariate analyses.ResultsAt diagnosis, we found that plasma levels of interleukin-6 (IL-6) and the chemokines (C-X3-C) motif legend CXCL9 and CXCL13 in CTD-PAH patients were significantly increased, compared with HCs. In idiopathic PAH patients the levels of tumor growth factor-β (TGFβ), IL-10 and CXCL9 were elevated, compared with HCs. The increased CXCL9 and IL-8 concentrations in CETPH patients correlated significantly with decreased survival, suggesting that CXCL9 and IL-8 may be prognostic markers. After one year of treatment, IL-10, CXCL13 and TGFβ levels changed significantly in the PAH subgroups and CTEPH patients. Unbiased multivariate analysis revealed clustering of PH patients based on inflammatory mediators and clinical parameters, but did not separate the WHO subgroups. Importantly, these multivariate analyses separated patients with < 3 years and > 3 years survival, in particular when inflammatory mediators were combined with clinical parameters.DiscussionOur study revealed elevated plasma levels of inflammatory mediators in different PAH subgroups and CTEPH at baseline and at 1-year follow-up, whereby CXCL9 and IL-8 may prove to be prognostic markers for CTEPH patients. While this study is exploratory and hypothesis generating, our data indicate an important role for IL-8 and CXCL9 in CHD and CTEPH patients considering the increased plasma levels and the observed correlation with survival.ConclusionIn conclusion, our studies identified an inflammatory signature that clustered PH patients into WHO classification-independent subgroups that correlated with patient survival.

Highlights

  • Pulmonary hypertension (PH) is a debilitating disease characterized by structural remodeling of the arterial vasculature of the lung leading to increased vascularKoudstaal et al Respir Res (2021) 22:137 resistance and increased pulmonary arterial pressures, right ventricular (RV) hypertrophy, heart failure and death [1]

  • Plasma from patients at diagnosis and healthy controls (HC) were analyzed for the cytokines IL-1β, IL-6, IL-8, IL-10 and tumor growth factor-β (TGFβ), the chemokines CXCL9 and CXCL13 and vascular endothelial growth factor (VEGF) (Fig. 1)

  • Compared with HCs, plasma levels of IL-6 and IL-10 were significantly elevated in CTD-pulmonary arterial hypertension (PAH) and idiopathic PAH (IPAH) patients, respectively

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Summary

Introduction

Pulmonary hypertension (PH) is a debilitating disease characterized by structural remodeling of the arterial vasculature of the lung leading to increased vascularKoudstaal et al Respir Res (2021) 22:137 resistance and increased pulmonary arterial pressures, right ventricular (RV) hypertrophy, heart failure and death [1]. Lungs of idiopathic PAH (IPAH) patients (belonging to WHO subgroup 1 PH) display an increased inflammatory mark consisting of T and B lymphocytes, mast cells, dendritic cells and macrophages [13, 14]. Thrombotic lesions in CTEPH patients contain activated T and B lymphocytes, macrophages and neutrophils and patients display elevated levels of circulating cytokines and chemokines [18, 19]. These inflammatory mediators can contribute directly to recruitment of immune cells, activation and proliferation of pulmonary arterial smooth muscle cells, and endothelial dysfunction. We investigated whether the inflammatory profile of pulmonary hypertension patients changes over time and correlates with patient WHO subgroups or survival

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