Abstract
BackgroundInterstitial lung diseases (ILDs) are common in patients with connective tissue diseases (CTDs). Although the diagnosis of an underlying CTD in ILD (CTD-ILD) affects both prognosis and treatment, it is sometimes difficult to distinguish CTD-ILD from chronic fibrosing interstitial pneumonia (CFIP). B cell–activating factor belonging to the tumour necrosis factor family (BAFF) plays a crucial role in B cell development, survival, and antibody production.MethodsWe examined serum levels of BAFF, surfactant protein D (SP-D), and Krebs von den Lungen-6 (KL-6) in 33 patients with CTD-ILD, 16 patients with undifferentiated CTD-ILD, 19 patients with CFIP, and 26 healthy volunteers. And we analysed the relationship between serum BAFF levels and pulmonary function, as well as the expression of BAFF in the lung tissue of patients with CTD-ILD.ResultsSerum levels of BAFF were significantly higher in CTD-ILD patients compared to healthy subjects and CFIP patients. However, there were no significant differences in serum levels of SP-D and KL-6. Furthermore, serum BAFF levels in CTD-ILD patients were inversely correlated with pulmonary function. BAFF was strongly expressed in the lungs of CTD-ILD patients, but weakly in normal lungs.DiscussionThis is the first study to demonstrate that serum BAFF levels were significantly higher in CTD-ILD patients compared to healthy subjects and CFIP patients. Furthermore, serum BAFF levels were correlated with pulmonary function. We consider that serum BAFF levels in patients with CTD-ILD reflect the presence of ILDs disease activity and severity.ConclusionThese finding suggest that BAFF may be a useful marker for distinguishing CTD-ILD from CFIP.
Highlights
Interstitial lung diseases (ILDs) are common in patients with connective tissue diseases (CTDs)
This is the first study to demonstrate that serum BAFF levels were significantly higher in CTD in ILD (CTD-ILD) patients compared to healthy subjects and chronic fibrosing interstitial pneumonia (CFIP) patients
Serum BAFF levels in patients with CTD-ILD compared to patients with CFIP or UCTD and control subjects
Summary
Interstitial lung diseases (ILDs) are common in patients with connective tissue diseases (CTDs). The diagnosis of an underlying CTD in ILD (CTD-ILD) affects both prognosis and treatment, it is sometimes difficult to distinguish CTD-ILD from chronic fibrosing interstitial pneumonia (CFIP). Connective tissue diseases (CTDs) are inflammatory, immune-mediated disorders that can cause a large variety of pulmonary complications, including bronchiolitis, pleuritis, and pulmonary hypertension. Interstitial lung diseases (ILDs) are a common form of pulmonary involvement associated with CTDs that is characterised by various patterns of inflammation and fibrosis [1]. The prognosis of patients with CTD-ILD is generally more favourable than those with idiopathic interstitial pneumonias (IIPs) [1,2,3]. Since a diagnosis of underlying CTDs affects prognosis and treatment, it is crucial to evaluate for underlying CTDs in patients with
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