Investigating Interferon type I responses in patients with suspected giant cell arteritis and polymyalgia rheumatica

• Published in: Clinical and experimental immunology
• Main Authors: van Nieuwland, Marieke, Mulder, A H Leontine, Colin, Edgar M, Alves, Celina, van Bon, Lenny, Brouwer, Elisabeth
• Format: Journal Article
• Language: English
• Published: England 04.10.2024
• Subjects: Cytokines; Chemokines; Vasculitis
• ISSN: 0009-9104; 1365-2249; 1365-2249
• DOI: 10.1093/cei/uxae085

Giant cell arteritis (GCA) and polymyalgia rheumatica (PMR) are closely related inflammatory disorders. Easily measurable biomarkers defining active disease and identifying patients in need of glucocorticoid (GC) sparing treatment options are highly desired. Interferon type I (IFN-I) might be involved in disease pathology, however evidence is limited. This study explores a systemic IFN-I signature and expression of IFN-I markers in GCA and PMR patients. Treatment naive GCA and PMR patients, and PMR patients with GC treatment were included. Patients suspected of but not diagnosed with GCA were used as controls. Five relevant IFN-I stimulated genes (ISGs) were identified in literature and relative expression levels were determined using RT-qPCR in PBMCs. An IFN-I score was generated. Serum levels of IFN-I induced CXCL10 and Galactin-9 were determined by multiplex immunoassay. There were no differences in IFN-I scores between the groups. An IFN-I signature was observed in 0/9 controls, 2/11 GCA patients, 4/20 treatment naive PMR patients and 2/10 PMR patients with treatment. Serum CXCL10 and Galactin-9 were not increased in GCA or PMR patients compared to control patients. Treated PMR patients had lower CXCL10 levels (423.2 pg/ml (375.1-491.1)) compared to treatment naive PMR patients (641.8 pg/ml (552.8-830.6)). An IFN-I signature does not distinguish GCA and PMR patients from controls. Also, IFN-I induced serum markers are not upregulated in GCA and PMR patients. Easily measurable IFN-I induced serum markers will therefore probably not aid in diagnosis and additional treatment options in newly diagnosed GCA and PMR patients.