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Antisynthetase antibodies in clinical laboratories: the importance of clinical correlation and indirect immunofluorescence. Response to: Comment on: ‘Idiopathic inflammatory myopathies and antisynthetase syndrome: contribution of antisynthetase antibodies to improve current classification criteria’ by Greco et al’ by Knitza et al
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  1. Martin Greco1,
  2. Mª Jesus García de Yébenes2,
  3. Inmaculada Alarcón3,
  4. Anahy María Brandy-García4,
  5. Íñigo Rúa-Figueroa1,
  6. Estibaliz Loza2,
  7. Loreto Carmona2
  1. 1 Rheumatology, Hospital Universitario de Gran Canaria Dr Negrin, Las Palmas de Gran Canaria, Spain
  2. 2 Institute for Musculoskeletal Health, Madrid, Spain
  3. 3 Biochemical Department, Autoimmunity Laboratory, Las Palmas de Gran Canaria, Spain
  4. 4 Rheumatology Department, Hospital Universitario Central de Asturias, Oviedo, Spain
  1. Correspondence to Dr Martin Greco, Rheumatology, Hospital Universitario de Gran Canaria Dr Negrin, Las Palmas de Gran Canaria 35010, Spain; martin-greco{at}hotmail.com

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We have recently published a retrospective two centres study of 37 patients with clinical suspicion of idiopathic inflammatory myopathies (IIM) or antisynthetase syndrome (ASSD), and antiaminoacyl-transfer RNA synthetase (ARS) autoantibodies in the myositis immunoblot. In it, we discussed the role of the ARS in the IIM and the ASSD classification criteria, and a possible overlapping between both of them.1

Regarding the detection of ARS, previous studies have shown differences in the specificity between different commercial assays; thus, in agreement with the highly appropriate commentaries raised by Knitza et al on our report, we consider that a careful interpretation of them is mandatory.2 3 In this way, in a recent review Damoiseaux et al proposed that to safeguard a high specificity of myositis-specific autoantibodies in multispecific-assays, it could be useful1: to establish adequate cut-off values in the immunoblot2; to correlate the results with another monospecific-assay (ie, ELISA …

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