TY - JOUR
T1 - Ultrasensitive interferons quantification reveals different cytokine profile secretion in inflammatory myopathies and can serve as biomarkers of activity in dermatomyositis
AU - Bolko, Loïs
AU - Anquetil, Céline
AU - Llibre, Alba
AU - Maillard, Solène
AU - Amelin, Damien
AU - Dorgham, Karim
AU - Bondet, Vincent
AU - Landon-Cardinal, Océane
AU - Toquet, Ségolène
AU - Mariampillai, Kuberaka
AU - Malatre, Samuel
AU - Mahoudeau, Alexandrine
AU - Hervier, Baptiste
AU - Rodero, Mathieu
AU - Gorochov, Guy
AU - Duffy, Darragh
AU - Benveniste, Olivier
AU - Allenbach, Yves
N1 - Publisher Copyright:
Copyright © 2025 Bolko, Anquetil, Llibre, Maillard, Amelin, Dorgham, Bondet, Landon-Cardinal, Toquet, Mariampillai, Malatre, Mahoudeau, Hervier, Rodero, Gorochov, Duffy, Benveniste and Allenbach.
PY - 2025/1/1
Y1 - 2025/1/1
N2 - Objective: The objective of this study was to evaluate the presence of different types of interferon in idiopathic inflammatory myopathies (IIM) and their subgroups using ultrasensitive cytokine detection techniques (SIMOA) and to assess their potential as activity biomarkers. Methods: Disease activity was measured at the time of serum collection and assessed by manual muscle testing eight (MMT8 score 0-150), muscle enzymes to calculate the Physician Global Assessment (PGA) (0-10). Patients were classified as active if PGA>5.Serum IFN-α and IFN-γ levels was measured using the single molecule array (SIMOA) technique. Serum IFN-β level was measured by Elisa. Correlation between IFN levels and disease activity were performed. Results: We included 242 IIM patients and found a good correlation between type I Interferon (IFN) and dermatomyositis disease activity. IFN-α and IFN-β was highly correlated with disease activity (r=0.76 and r=0,58). To evaluate whether the different types of Interferons could serve as biomarkers of activity, we generated ROC curves. Patients with active DM had a higher median IFN-α level (0.49 pg/ml [0.1-3.7]) compared with non-active patients (0.03 pg/ml [0.01-0.07] p<0.05). The area under the curve was 0.90 IC95 (0.76-0.97) p<0.05. Furthermore, Myositis-specific antibodies appear to be associated with a different secretion profile; patients with anti-MDA 5 antibodies had higher level of IFN-α than most other antibodies (6.58 vs 0.14 p<0.005). NXP2 had higher IFN-β level than patients with Tif1γ antibodies. Conclusion: Serum IFN-α level measured by SIMOA is a reliable biomarker of DM activity. Myositis-specific antibodies appear to be associated with a different secretion profile. This data needs to be confirmed in order to select the good therapeutics strategies in DM.
AB - Objective: The objective of this study was to evaluate the presence of different types of interferon in idiopathic inflammatory myopathies (IIM) and their subgroups using ultrasensitive cytokine detection techniques (SIMOA) and to assess their potential as activity biomarkers. Methods: Disease activity was measured at the time of serum collection and assessed by manual muscle testing eight (MMT8 score 0-150), muscle enzymes to calculate the Physician Global Assessment (PGA) (0-10). Patients were classified as active if PGA>5.Serum IFN-α and IFN-γ levels was measured using the single molecule array (SIMOA) technique. Serum IFN-β level was measured by Elisa. Correlation between IFN levels and disease activity were performed. Results: We included 242 IIM patients and found a good correlation between type I Interferon (IFN) and dermatomyositis disease activity. IFN-α and IFN-β was highly correlated with disease activity (r=0.76 and r=0,58). To evaluate whether the different types of Interferons could serve as biomarkers of activity, we generated ROC curves. Patients with active DM had a higher median IFN-α level (0.49 pg/ml [0.1-3.7]) compared with non-active patients (0.03 pg/ml [0.01-0.07] p<0.05). The area under the curve was 0.90 IC95 (0.76-0.97) p<0.05. Furthermore, Myositis-specific antibodies appear to be associated with a different secretion profile; patients with anti-MDA 5 antibodies had higher level of IFN-α than most other antibodies (6.58 vs 0.14 p<0.005). NXP2 had higher IFN-β level than patients with Tif1γ antibodies. Conclusion: Serum IFN-α level measured by SIMOA is a reliable biomarker of DM activity. Myositis-specific antibodies appear to be associated with a different secretion profile. This data needs to be confirmed in order to select the good therapeutics strategies in DM.
KW - Anti-synthetase syndrom
KW - biomarker
KW - dermatomyositis
KW - immune mediated necrotizing myopathie
KW - inclusion body myositis
KW - interferon
UR - http://www.scopus.com/inward/record.url?scp=85219189225&partnerID=8YFLogxK
U2 - 10.3389/fimmu.2025.1529582
DO - 10.3389/fimmu.2025.1529582
M3 - Article
AN - SCOPUS:85219189225
SN - 1664-3224
VL - 16
JO - Frontiers in Immunology
JF - Frontiers in Immunology
M1 - 1529582
ER -