Extended report
Autoantibody profiles in the sera of European patients with
myositis
R Brouwera, G J D Hengstmanb, W Vree Egbertsa, H Ehrfeldc, B Bozicd, A Ghirardelloe, G Grøndalf, M Hietarintag, D Isenbergh, J R Kaldeni, I Lundbergf, H Moutsopoulosj, P Roux-Lombardk, J Vencovskyl, A Wikmanf, H P Seeligc, B G M van Engelenb, W J van Venrooija
a Department of
Biochemistry, University of Nijmegen, Nijmegen, The Netherlands, b Neuromuscular Centre Nijmegen, Institute of
Neurology, University Hospital Nijmegen, Nijmegen, The Netherlands, c Institute of Immunology and Molecular Genetics,
Karlsruhe, Germany, d Department
of Rheumatology, Ljubljana, Slovenia, e Division of Rheumatology, Padova, Italy, f Department of Rheumatology,
Stockholm, Sweden, g Department of Medicine, Turku University,
Finland, h Bloomsbury
Rheumatology Unit, London, United Kingdom, i Institute of Clinical Immunology,
Erlangen-Nürnberg, Germany, j Department of Pathophysiology, National
University, Athens, Greece, k Division of Immunology and Allergy, University
of Geneva, Switzerland, l Institute
of Rheumatology, Prague, Czech Republic
Correspondence to: Dr W J van Venrooij, Department of Biochemistry, University of Nijmegen, PO Box 9101, NL-6500 HB, Nijmegen, The Netherlands w.vanvenrooij{at}bioch.kun.nl Accepted 22 August 2000
OBJECTIVE
To determine
the prevalence of myositis specific
autoantibodies (MSAs) and several myositis
associated autoantibodies (MAAs) in a large
group of patients with myositis.
METHODS
A total of 417 patients with myositis from 11 European countries (198 patients with
polymyositis (PM), 181 with dermatomyositis (DM), and 38 with inclusion
body myositis (IBM)) were serologically analysed by immunoblot, enzyme
linked immunosorbent assay (ELISA) and/or immunoprecipitation.
RESULTS
Autoantibodies
were found in 232 sera (56%), including 157 samples (38%) which
contained MSAs. The most commonly detected MSA was anti-Jo-1 (18%).
Other anti-synthetase, anti-Mi-2, and anti-SRP autoantibodies were
found in 3%, 14%, and 5% of the sera, respectively. A relatively
high number of anti-Mi-2 positive PM sera were found (9% of PM sera).
The most commonly detected MAA was anti-Ro52 (25%). Anti-PM/Scl-100,
anti-PM/Scl-75, anti-Mas, anti-Ro60, anti-La, and anti-U1 snRNP
autoantibodies were present in 6%, 3%, 2%, 4%, 5%, and 6% of the
sera, respectively. Remarkable associations were noticed between
anti-Ro52 and anti-Jo-1 autoantibodies and, in a few sera, also between
anti-Jo-1 and anti-SRP or anti-Mi-2 autoantibodies.
CONCLUSIONS
The
incidence of most of the tested autoantibody activities in this large
group of European patients is in agreement with similar studies of
Japanese and American patients. The relatively high number of PM sera
with anti-Mi-2 reactivity may be explained by the use of multiple
recombinant fragments spanning the complete antigen. Furthermore, our
data show that some sera may contain more than one type of MSA and
confirm the strong association of anti-Ro52 with anti-Jo-1 reactivity.
© 2001 by Annals of the Rheumatic Diseases
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