Inefficacy of infliximab in primary Sjögren's syndrome: results of the randomized, controlled Trial of Remicade in Primary Sjögren's Syndrome (TRIPSS).

OBJECTIVE There is no effective treatment for patients with primary Sjögren's syndrome (SS). Since tumor necrosis factor alpha (TNF alpha) could be a key element in the pathogenesis of primary SS, we conducted a multicenter, randomized, double-blind, placebo-controlled trial to evaluate the effect of infliximab in primary SS. METHODS A total of 103 patients with primary SS were randomly assigned to receive infliximab infusions (5 mg/kg) or placebo at weeks 0, 2, and 6 and were followed up for 22 weeks. All patients fulfilled the new American-European Consensus Group criteria for SS and had active disease as assessed by values >50 mm on 2 of 3 visual analog scales (VAS) (0-100 mm) that evaluated joint pain, fatigue, and buccal, ocular, skin, vaginal, or bronchial dryness. A favorable overall response was defined as the patient having > or =30% improvement between weeks 0 and 10 in the values on 2 of the 3 VAS. Secondary end points were values on each VAS separately, the number of tender and swollen joints, the basal salivary flow rate, results of the Schirmer test for lacrimal gland function, the focus score on labial salivary gland biopsy, the level of C-reactive protein, and the erythrocyte sedimentation rate evaluated at weeks 0, 10, and 22, as well as quality of life evaluated by use of the generic Short Form 36 questionnaire administered at weeks 0, 10, and 22. RESULTS At week 10, 26.5% of patients receiving placebo and 27.8% of patients treated with infliximab had a favorable overall response (P = 0.89), and at week 22, 20.4% of the placebo group and 16.7% of the infliximab group had a favorable response (P = 0.62). In addition, the 2 groups did not differ in any of the secondary end points over the 22 weeks of the trial. Severe adverse events reported in the infliximab group did not differ from those observed in previous studies. CONCLUSION This randomized, double-blind, placebo-controlled study of an anti-TNF agent did not show any evidence of efficacy of infliximab in primary SS.

[1]  J. Tschopp,et al.  TNF Deficiency Fails to Protect BAFF Transgenic Mice against Autoimmunity and Reveals a Predisposition to B Cell Lymphoma1 , 2004, The Journal of Immunology.

[2]  E. Veys,et al.  Antinuclear antibodies following infliximab treatment in patients with rheumatoid arthritis or spondylarthropathy. , 2003, Arthritis and rheumatism.

[3]  X. Mariette Current and potential treatments for primary Sjögren's syndrome. , 2002, Joint, bone, spine : revue du rhumatisme.

[4]  R. Jonsson,et al.  Classification criteria for Sjögren's syndrome: a revised version of the European criteria proposed by the American-European Consensus Group , 2002, Annals of the rheumatic diseases.

[5]  R. Kiss,et al.  Infliximab in patients with primary Sjögren's syndrome: a pilot study. , 2001, Arthritis and rheumatism.

[6]  Y. Konttinen,et al.  Tumor necrosis factor-alpha and receptors for it in labial salivary glands in Sjögren's syndrome. , 2001, Clinical and experimental rheumatology.

[7]  M. Rischmueller,et al.  Inhibitory effects of muscarinic receptor autoantibodies on parasympathetic neurotransmission in Sjögren's syndrome. , 2000, Arthritis and rheumatism.

[8]  J. Concato,et al.  Randomized, controlled trials, observational studies, and the hierarchy of research designs. , 2000, The New England journal of medicine.

[9]  T. Sugiyama,et al.  Interferon gamma and tumor necrosis factor alpha induce Fas expression and anti-Fas mediated apoptosis in a salivary ductal cell line. , 2000, Clinical and experimental rheumatology.

[10]  U. Abel,et al.  The role of randomization in clinical studies: myths and beliefs. , 1999, Journal of clinical epidemiology.

[11]  D. Wakefield,et al.  Chemokine expression and leucocyte infiltration in Sjögren's syndrome. , 1998, British journal of rheumatology.

[12]  M. Lindsay,et al.  Synergy between tumor necrosis factor alpha and interleukin 1beta in inducing transcriptional down-regulation of muscarinic M2 receptor gene expression. Involvement of protein kinase A and ceramide pathways. , 1996, The Journal of biological chemistry.

[13]  R. Fox,et al.  Sjögren's syndrome , 1995, The Lancet.

[14]  T. Perneger,et al.  Validation of a French-language version of the MOS 36-Item Short Form Health Survey (SF-36) in young healthy adults. , 1995, Journal of clinical epidemiology.

[15]  J. Abrams,et al.  Cytokine mRNA expression in salivary gland biopsies of Sjögren's syndrome. , 1994, Journal of immunology.

[16]  R. Fox,et al.  Pathogenesis of Sjögren's syndrome. , 1992, Rheumatic diseases clinics of North America.

[17]  R. Akın,et al.  Sj??gren??s syndrome , 1975 .