Heterogeneous Nuclear Ribonucleoprotein H1, a Novel Nuclear Autoantigen

Author:

Van den Bergh Karolien1,Hooijkaas Herbert2,Blockmans Daniel3,Westhovens René4,Op De Beéck Katrijn1,Verschueren Patrick4,Dufour Diana2,van de Merwe Joop P5,Fijak Monika6,Klug Jörg6,Michiels Georges1,Devogelaere Benoit7,De Smedt Humbert7,Derua Rita8,Waelkens Etienne8,Blanckaert Norbert1,Bossuyt Xavier1

Affiliation:

1. Laboratory Medicine, Immunology, University Hospitals Leuven, Belgium

2. Department of Immunology, Erasmus MC, University Medical Center Rotterdam, the Netherlands

3. General Internal Medicine, University Hospitals Leuven, Belgium

4. Rheumatology, University Hospitals Leuven, Belgium

5. Department of Immunology and Department of Internal Medicine, Erasmus Medical Center Rotterdam, the Netherlands

6. Department of Anatomy and Cell Biology, Justus-Liebig-University of Giessen, Germany

7. Department of Molecular Cell Biology (Laboratory of Molecular and Cellular Signalling), Catholic University of Leuven, Belgium

8. Department of Molecular Cell Biology (Laboratory of Protein Phosphorylation and Proteomics) and Biomacs, Catholic University of Leuven, Belgium

Abstract

AbstractBackground: Serum samples from patients with autoimmune connective tissue diseases that show a finely speckled antinuclear antibody (ANA) on indirect immune-fluorescence often have antibodies against unknown nuclear target antigens. To search for such autoantigens we applied a proteomic approach using sera from patients with a high ANA titer (≥640) and finely speckled fluorescence but in whom no antibodies to extractable nuclear antigens (ENA) could be identified.Methods: Using an immunoproteomics approach we identified heterogeneous nuclear ribonucleoprotein H1 (hnRNP H1) as a novel nuclear target of autoantibody response.Results: Recombinant rat hnRNP H1 reacted in Western blot analyses with 48% of 93 sera from patients with primary Sjögren syndrome and with 5.2% of 153 sera from patients with other connective tissue diseases (diseased controls). For comparison, the diagnostic sensitivity and specificity of anti–Sjögren syndrome A (SSA) antibodies for primary Sjögren syndrome in the same patient cohort were 88.2% and 76.3%, respectively. Interestingly, 5 of 11 primary Sjögren syndrome patients with no anti-SSA or anti-SSB antibodies had anti–hnRNP H1 antibodies. Anti–hnRNP H1 antibodies were preabsorbed by hnRNP H1, as demonstrated by indirect immunofluorescence. In an evaluation of the presence of anti–hnRNP H1 antibodies in 188 consecutive samples submitted to the clinical laboratory with positive ANA (titer ≥160), anti–hnRNP H1 antibodies were found in 3 of 7 (2 primary and 5 secondary) Sjögren syndrome patients and in 8.3% of the diseased controls.Conclusions: HnRNP H1 is a newly discovered autoantigen that could become an additional diagnostic marker.

Funder

UCB

Publisher

Oxford University Press (OUP)

Subject

Biochemistry, medical,Clinical Biochemistry

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