TY - JOUR
T1 - Anti–Cytosolic 5′-Nucleotidase 1A Autoantibodies Are Absent in Juvenile Dermatomyositis
AU - Rietveld, Anke
AU - Wienke, Judith
AU - Visser, Eline
AU - Vree Egberts, Wilma
AU - Schlumberger, Wolfgang
AU - van Engelen, Baziel
AU - van Royen-Kerkhof, Annet
AU - Lu, Hui
AU - Wedderburn, Lucy
AU - Saris, Christiaan
AU - Tansley, Sarah
AU - Pruijn, Ger
N1 - Funding Information:
We thank the Dutch Juvenile Myositis Consortium, with Sylvia Kamphuis, Esther Hoppenreijs, Ellen Schatorjé, Wineke Armbrust, Merlijn van den Berg, Petra Hissink Muller and Annette van Dijk-Hummelman, for their help and support with patient inclusion and sample and data collection.
Publisher Copyright:
© 2021 The Authors. Arthritis & Rheumatology published by Wiley Periodicals LLC on behalf of American College of Rheumatology.
PY - 2021/7
Y1 - 2021/7
N2 - Objective: To assess anti–cytosolic 5′-nucleotidase 1A (anti–cN-1A) autoantibodies in children with juvenile dermatomyositis (DM) and healthy controls, using 3 different methods of antibody detection, as well as verification of the results in an independent cohort. Methods: Anti–cN-1A reactivity was assessed in 34 Dutch juvenile DM patients and 20 healthy juvenile controls using the following methods: a commercially available full-length cN-1A enzyme-linked immunosorbent assay (ELISA), a synthetic peptide ELISA, and immunoblotting with a lysate from cN-1A–expressing HEK 293 cells. Sera from juvenile DM patients with active disease and those with disease in remission were analyzed. An independent British cohort of 110 juvenile DM patients and 43 healthy juvenile controls was assessed using an in-house full-length cN-1A ELISA. Results: Anti–cN-1A reactivity was not present in sera from juvenile DM patients or healthy controls when tested with the commercially available full-length cN-1A ELISA or by immunoblotting, in either active disease or disease in remission. Additionally, in the British juvenile DM cohort, anti–cN-1A reactivity was not detected. Three Dutch juvenile DM patients had weakly positive results for 1 of 3 synthetic cN-1A peptides measured by ELISA. Conclusion: Juvenile DM patients and young healthy individuals did not show anti–cN-1A reactivity as assessed by different antibody detection techniques.
AB - Objective: To assess anti–cytosolic 5′-nucleotidase 1A (anti–cN-1A) autoantibodies in children with juvenile dermatomyositis (DM) and healthy controls, using 3 different methods of antibody detection, as well as verification of the results in an independent cohort. Methods: Anti–cN-1A reactivity was assessed in 34 Dutch juvenile DM patients and 20 healthy juvenile controls using the following methods: a commercially available full-length cN-1A enzyme-linked immunosorbent assay (ELISA), a synthetic peptide ELISA, and immunoblotting with a lysate from cN-1A–expressing HEK 293 cells. Sera from juvenile DM patients with active disease and those with disease in remission were analyzed. An independent British cohort of 110 juvenile DM patients and 43 healthy juvenile controls was assessed using an in-house full-length cN-1A ELISA. Results: Anti–cN-1A reactivity was not present in sera from juvenile DM patients or healthy controls when tested with the commercially available full-length cN-1A ELISA or by immunoblotting, in either active disease or disease in remission. Additionally, in the British juvenile DM cohort, anti–cN-1A reactivity was not detected. Three Dutch juvenile DM patients had weakly positive results for 1 of 3 synthetic cN-1A peptides measured by ELISA. Conclusion: Juvenile DM patients and young healthy individuals did not show anti–cN-1A reactivity as assessed by different antibody detection techniques.
UR - http://www.scopus.com/inward/record.url?scp=85106295646&partnerID=8YFLogxK
U2 - 10.1002/art.41660
DO - 10.1002/art.41660
M3 - Article
C2 - 33497020
AN - SCOPUS:85106295646
SN - 2326-5191
VL - 73
SP - 1329
EP - 1333
JO - Arthritis and Rheumatology
JF - Arthritis and Rheumatology
IS - 7
ER -