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Sensitivity of the Phadia EliA connective tissue disease screen for less common disease-specific autoantibodies
  1. Jennifer C Parker,
  2. Christopher C Bunn
  1. Department of Clinical Immunology, Royal Free Hospital, London, UK
  1. Correspondence to Dr Chris Bunn, Department of Clinical Immunology, Royal Free Hospital, Pond Street, London NW3 2QG, UK; c.bunn{at}medsch.ucl.ac.uk

Abstract

Aim To evaluate the sensitivity of a commercial autoantibody screening method (Phadia EliA connective tissue disease (CTD) screen) for the detection of less common antibody specificities associated with connective tissue disease.

Methods 399 sera positive for anti-PM/Scl (n=102), anti-RNA polymerase III (n=199), anti-fibrillarin (n=50), anti-Mi-2 (n=12), anti-proliferating cell nuclear antigen (PCNA) (n=13) and anti-ribosomal P (n=23) were analysed using the solid phase assay. Each well was coated with the respective antigens for these autoantibodies and also with the antigens Ro, La, Jo-1, Scl-70, CENP-B, U1-RNP, Sm and native DNA.

Results All the anti-ribosomal P, anti-PCNA and anti-Mi-2 sera and 94% of the anti-PM/Scl sera were positive. For anti-fibrillarin, 36 (68%) were positive and 12 (22%) were equivocal. For anti-RNA polymerase III, 131 (67%) were positive, 23 (11%) were equivocal and 45 (22%) were negative.

Conclusions The sensitivity of the Phadia EliA CTD screen is currently insufficient for the assay to be used as a screening test for anti-fibrillarin and anti-RNA polymerase III, but appears to be satisfactory for the other autoantibodies tested.

  • Autoantibodies
  • autoimmune laboratory investigations
  • connective tissue disease
  • immunoassay

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Footnotes

  • The authors contributed equally to the design and execution of the study and the preparation of the manuscript.

  • Competing interests None to declare.

  • Provenance and peer review Not commissioned; externally peer reviewed.

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