The importance of detecting anti-DFS70 in routine clinical practice: comparison of different care settings

Clin Chem Lab Med. 2018 Jun 27;56(7):1090-1099. doi: 10.1515/cclm-2017-0541.

Abstract

Background: Screening for antinuclear antibodies by indirect immunofluorescence (ANA-IIF) is essential in the diagnostic workup of ANA-associated autoimmune rheumatic diseases (AARDs). However, also healthy individuals may test positive, making the interpretation challenging. Recent reports suggest that dense fine speckled 70 antibodies (anti-DFS70) may facilitate this challenge. Here, we investigate their clinical importance based on data from four Belgian laboratories (one primary, two secondary and one tertiary care).

Methods: At least one specific DFS70 assay (DFS70 IgG ELISA or lineblot [Euroimmun, full length antigen] and/or DFS70 IgG CLIA [Inova Diagnostics, truncated antigen]) was performed on four consecutive cohorts of homogeneous-like ANA-IIF samples (n=697). Co-occurrence with AARD-specific ANA and clinical information were documented in the anti-DFS70-positive samples.

Results: Using a combination of solid phase techniques, we found between 7.6% and 26% anti-DFS70 in the different cohorts. Focusing on anti-DFS70 CLIA-positive samples without co-occurrence of AARD-specific ANA, we observed a trend towards lower frequency in tertiary (8% [p=0.0786]) and secondary care (12% [p=0.1275] and 6% [p<0.001]) compared to primary care (21%). Moreover, in this specific subpopulation, AARD was less frequent (0%-50% compared to 6%-77% in the total anti-DFS70-positive group).

Conclusions: Anti-DFS70 prevalence depends on the applied assay and care setting. Our data suggest that, for an ANA-IIF-positive patient, it is rather the absence of AARD-associated ANA and clinical symptoms that contribute to the exclusion of AARD than the presence of anti-DFS70. Nevertheless, isolated anti-DFS70 helps to clarify positive ANA-IIF results, especially if pretest probability for AARD is low.

Keywords: anti-DFS70/LEDGF; antinuclear antibodies; systemic rheumatic autoimmune diseases.

Publication types

  • Comparative Study
  • Multicenter Study

MeSH terms

  • Adaptor Proteins, Signal Transducing / immunology*
  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Antibodies, Antinuclear / blood*
  • Antibodies, Antinuclear / immunology
  • Autoimmune Diseases / diagnosis*
  • Belgium
  • Female
  • Fluorescent Antibody Technique, Indirect / methods
  • Humans
  • Male
  • Middle Aged
  • Rheumatic Diseases / diagnosis*
  • Transcription Factors / immunology*
  • Young Adult

Substances

  • Adaptor Proteins, Signal Transducing
  • Antibodies, Antinuclear
  • PSIP1 protein, human
  • Transcription Factors