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ORIGINAL ARTICLE

Serum levels of interleukin-32 and interleukin-6 in granulomatosis with polyangiitis and microscopic polyangiitis: association with clinical and biochemical findings

Joanna Krajewska (Wojciechowska)1, Katarzyna Kos·cielska-Kasprzak2, Wojciech Krajewski3, Krzysztof Morawski1

1 Medical University in Wrocław, Department and Clinic of Otolaryngology, Head and Neck Surgery, Borowska 213 Street, Wrocław Poland
2 Medical University in Wrocław, Department and Clinic of Nephrology and Transplantation Medicine, Borowska 213 Street, Wrocław Poland
3 Medical University in Wrocław, Department and Clinic of Urology and Urological Oncology, Borowska 213 Street, Wrocław Poland

* Corresponding Authors: Joanna Krajewska (Wojciechowska), email; email

European Cytokine Network 2019, 30(4), 151-159. https://doi.org/10.1684/ecn.2019.0439

Abstract

Background: Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis is an autoimmune disorder of unknown etiology with dysregulated cytokines levels. Objectives: The main aim of this study was to assess the clinical correlation between antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis, granulomatosis with polyangiitis (GPA) serum levels of the microscopic polyangiitis (MPA), serum levels of the proinflammatory cytokines, interleukin (IL)-32 and interleukin-6. Methods: Study included 71 patients, 47 with GPA and 24 with MPA. Serum IL-32 and IL-6 concentrations were analyzed in all patients, and compared with levels observed in 10 controls. IL-32 and IL-6 were evaluated using DuoSet and Quantikine HS ELISA, respectively. IL-32 and IL-6 concentrations were correlated with disease-related clinical and laboratory findings. Results: IL-32 and IL-6 levels were significantly higher in GPA and MPA than in controls, especially IL-32 levels in GPA were elevated. IL-32 concentrations correlated positively with antiproteinase 3 - ANCA (PR3-ANCA) levels in GPA (P < 0.0001), and with anti-myeloperoxidase ANCA (MPO-ANCA) inMPA (P = 0.049). IL-32 levels correlated positively with disease activity in GPA andMPA (P < 0.0001). GPA patients with pulmonary, cutaneous, and musculoskeletal involvement presented the highest IL-6 serum levels. Cutaneous manifestations correlated positively with IL-6 levels in MPA patients (P = 0.05). ANCA-positive patients with GPA expressed significantly high IL-6 levels (P = 0.036). No significant difference in IL-32 values was observed between ANCA-positive and ANCA-negative patients.Conclusions: Patients with GPA andMPA present higher serum IL-32 and IL-6 levels than controls. IL-32 levels correlate positively with disease activity.

Keywords

granulomatosis with polyangiitis, interleukin-6, interleukin-32, microscopic polyangiitis, vasculitis, ANCA

Cite This Article

APA Style
(Wojciechowska), J.K., Kos·cielska-Kasprzak, K., Krajewski, W., Morawski, K. (2019). Serum levels of interleukin-32 and interleukin-6 in granulomatosis with polyangiitis and microscopic polyangiitis: association with clinical and biochemical findings. European Cytokine Network, 30(4), 151–159. https://doi.org/10.1684/ecn.2019.0439
Vancouver Style
(Wojciechowska) JK, Kos·cielska-Kasprzak K, Krajewski W, Morawski K. Serum levels of interleukin-32 and interleukin-6 in granulomatosis with polyangiitis and microscopic polyangiitis: association with clinical and biochemical findings. Eur Cytokine Network. 2019;30(4):151–159. https://doi.org/10.1684/ecn.2019.0439
IEEE Style
J.K. (Wojciechowska), K. Kos·cielska-Kasprzak, W. Krajewski, and K. Morawski, “Serum levels of interleukin-32 and interleukin-6 in granulomatosis with polyangiitis and microscopic polyangiitis: association with clinical and biochemical findings,” Eur. Cytokine Network, vol. 30, no. 4, pp. 151–159, 2019. https://doi.org/10.1684/ecn.2019.0439



cc Copyright © 2019 The Author(s). Published by Tech Science Press.
This work is licensed under a Creative Commons Attribution 4.0 International License , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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