Abstract

Dendritic cells (DCs) are critical effectors of innate and adaptive immunity playing crucial roles in autoimmune responses. We previously showed that blood DC numbers were reduced in autoimmune antineutrophil cytoplasmic autoantibody-associated vasculitis (AAV). Here, we assessed toll-like receptor (TLR) responsiveness of blood DCs from patients with granulomatosis with polyangiitis (GPA) or microscopic polyangiitis (MPA). Blood samples from healthy controls (HCs), GPA, or MPA patients, without treatment, during acute phase (AP) or remission phase (RP) were analyzed. Cytokine production by DCs and T cells was assessed on whole blood by flow cytometry after TLRs or polyclonal stimulation, respectively. We first showed that GPA and MPA are associated with a decreased blood DC number during AP. Conventional DCs (cDCs) from patients with GPA and MPA in AP exhibited a profound decrease of IL-12/IL-23p40 production after TLR3, 4, or 7/8 stimulation compared to patients in remission and HC, with a return to normal values in RP. TNFα secretion was also affected, with a decrease in cDCs from GPA patients in AP after TLR3 stimulation but an increase after TLR7/8 stimulation. By contrast, the responsiveness of plasmacytoid DCs to TLR7 and 9 was only marginally affected. Finally, we observed that IFNγ-producing CD4+ T cell frequency was significantly lower in AP-GPA patients than in HC. We describe, for the first time, a dysregulated response to TLRs of circulating DCs in AAV patients mostly affecting cDCs that exhibit an unexpected reduced inflammatory cytokine secretion possibly contributing to an altered Th cell response.

Highlights

  • Antineutrophil cytoplasmic autoantibody (ANCA)-associated vasculitis (AAV) are chronic and systemic autoimmune diseases characterized by small vessels inflammation and necrosis that can involve many organs and tissues

  • We previously reported that blood conventional DCs (cDCs) and plasmacytoid dendritic cells (pDCs) were strongly decreased in AAV patients during flares

  • We previously showed that patients with AAV displayed decreased numbers of circulating cDCs and pDCs during flares and to a lesser extent in remission phase (RP) [17]

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Summary

Introduction

Antineutrophil cytoplasmic autoantibody (ANCA)-associated vasculitis (AAV) are chronic and systemic autoimmune diseases characterized by small vessels inflammation and necrosis that can involve many organs and tissues (lungs, kidneys, heart, gut, nervous system, skin, etc.). ANCA are mostly directed to two neutrophil granule proteins, proteinase 3 (PR3) and myeloperoxidase (MPO) Their specificity is important in clinical practice as PR3-ANCA and MPO-ANCA are strongly associated with GPA and MPA, respectively, whereas the association with EGPA is much less clear [3, 5, 6]. Geographical disparities have been found with PR3-AAV being more prevalent in northwestern Europe and North America, while MPO-AAV is more prevalent in southern Europe, Asia, and the Pacific, possibly due to genetic and environmental factors [8]. This association extends to some clinical [9] and biological [12, 13] parameters

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