Blotting patterns of IgG anti-(U1)RNP antibodies in mixed connective tissue disease

Springer Science and Business Media LLC - Tập 16 - Trang 145-150 - 1996
A. Ghirardello1, A. Doria1,2, P. Vesco1, E. Vaccaro1, C. Bernardi1, C. Catani3, U. Fagiolo4, P. F. Gambari1
1Division of Rheumatology, Institute of Internal Medicine, University of Padova, Padova, Italy
2Cattedra e Divisione di Reumatologia, Istituto di Medicina Interna, Policlinico Universitario, Padova, Italy
3CNR Unit for Muscle Biology and Physiopathology, Department of Biochemical Sciences, University of Padova, Padova, Italy
4Institute of Internal Medicine, University of Padova, Padova, Italy

Tóm tắt

Serum reactivities towards individual U1 snRNP proteins were determined by immunoblotting in 32 patients with mixed connective tissue disease (MCTD). Time persistence of immunoblot profiles and clinical significance of anti-(U1)RNP antibody specificities were also investigated. IgG anti-(U1)RNP antibodies were found in the sera of 29 out of 32 patients (90.6%): 21 (65.6%) reacted with the 70-kD protein, 25 (78.1%) with A, 23 (71.9%) with C and 20 (62.5%) with B/B' proteins. None were reactive with the Sm-D peptide. Seventy kilodalton antibody specificity was strongly associated with a higher antinuclear antibody titre (>160) and slightly associated with disease activity; anti-B/B′ specificity was associated with lymphadenopathy. Anti-A, -C and -B/B′ antibodies were negatively associated with systemic lupus erythematosus (SLE) skin rashes. Two types of anti-(UI)RNP blotting patterns were selected: “full spectrum” (53.1% of cases) and a “partially/no reactive” one (46.9%). Such patterns were unchanged over time in 14 out of 16 cases prospectively examined (87.5%), while the pattern shifted from “full spectrum” to “partially/no reactive” in 2 cases (12.5%): in 1 after a prolonged clinical remission (≥4 years) and in the other following immunosuppressive therapy. The anti-(U1)RNP antibody immunoblot profile in MCTD patients consisted of various reactivities and remained unchanged over time in most cases. Antibody reactivity against the 70-kD protein represented the major Ul snRNP specificity. The various anti-(U1)RNP specific reactivities demonstrated poor clinical significance within MCTD. Thus, MCTD seems to be characterized by a longstanding serological heterogeneity whose reactivities do not apparently correspond to distinct features within the broad clinical spectrum of MCTD.

Tài liệu tham khảo

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