Abstract

IntroductionAntineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is characterised by the autoinflammation and necrosis of blood vessel walls. The renal involvement is commonly characterised by a pauci-immune crescentic glomerulonephritis (PiCGN) with a very rapid decline in renal function. Cathelicidin LL37, an endogenous antimicrobial peptide, has recently been implicated in the pathogenesis of autoimmune diseases. To assess whether serum LL37 reflects renal crescentic formation, we measured the serum levels of LL37 in AAV patients with and without crescentic glomerulonephritis (crescentic GN) as compared to healthy controls (HCs). We also analysed the correlation of the serum levels of LL37 and interferon-α (IFN-α) with the clinical characteristics of the patients.MethodsThe study population consisted of 85 AAV patients and 51 HCs. In 40 ANCA-positive patients, a parallel analysis was performed, including the assessment of LL37 and IFN-α levels in the serum and renal biopsies. Of those studied, 15 AAV patients had biopsy-proven crescentic GN, and 25 AAV patients lacked crescent formation. The serum levels of cathelicidin LL37 and IFN-α were both measured by ELISA, and the clinical and serological parameters were assessed according to routine procedures. Immunofluorescence staining was performed on frozen sections of kidney needle biopsies from AAV patients with crescentic GN.ResultsThe serum levels of LL37 and IFN-α were significantly increased in AAV patients with crescentic GN compared to AAV patients without crescentic formation and HCs, and patients with high LL37 and IFN-α levels were more likely to be in the crescentic GN group. The LL37 levels were positively correlated with the IFN-α levels, and both LL37 and IFN-α levels showed a positive correlation with serum creatinine and no correlation with complement C3. The renal tissue of crescentic GN patients showed expression of LL37 and IFN-α at the Bowman’s capsule and extracellular sites, suggesting the active release of LL37 and IFN-α.ConclusionsSignificantly higher levels of LL-37 and IFN-α were observed in AAV patients, particularly those with crescentic formation, and LL37 and IFN-α were expressed in the renal tissue of patients with crescentic GN. These data suggest that serum levels of LL37 and IFN-α may reflect both local renal inflammation and systemic inflammation.

Highlights

  • Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is characterised by the autoinflammation and necrosis of blood vessel walls

  • The serum levels of LL37 and IFN-α were significantly increased in AAV patients with crescentic GN compared to AAV patients without crescentic formation and Healthy control (HC), and patients with high LL37 and IFN-α levels were more likely to be in the crescentic GN group

  • Significantly higher levels of LL-37 and IFN-α were observed in AAV patients, those with crescentic formation, and LL37 and IFN-α were expressed in the renal tissue of patients with crescentic GN

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Summary

Introduction

Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is characterised by the autoinflammation and necrosis of blood vessel walls. Cathelicidin LL37, an endogenous antimicrobial peptide, has recently been implicated in the pathogenesis of autoimmune diseases. Anti-neutrophil cytoplasm antibody (ANCA)-associated vasculitis (AAV) represents a group of systemic autoimmune diseases including Wegener’s granulomatosis, microscopic polyangiitis, Churg–Strauss syndrome and renal limited vasculitis [1]. As an endogenous antimicrobial peptide, LL37 has recently been implicated in the pathogenesis of autoimmune diseases [5]. Autoinflammatory conditions such as psoriasis and systemic lupus erythematosus can be driven by plasmacytoid dendritic cells (pDCs), which produce large amounts of interferon alpha (IFNα) in the presence of DNA and cathelicidin LL37 [6,7]. DNA-containing LL37 was shown to be involved in the renal damage in AAV, with increased concentrations of IFNα in serum samples from individuals with active AAV [8]

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