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3.
Ann Rheum Dis ; 68(9): 1447-52, 2009 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-18782791

RESUMEN

OBJECTIVE: To evaluate the relevance of the blood B-cell subset profile for the diagnosis of Sjögren syndrome. METHODS: The distribution of mature blood B cells from Bm1 through Bm5 was determined in 161 patients, of whom 25 fulfilled the American-European Consensus Group criteria for primary SS (pSS), and 136 served as disease controls. RESULTS: The percentage of Bm2 and Bm2' cells was increased in the patients with pSS compared with 54 patients with rheumatoid arthritis (RA) and 18 with systemic lupus erythematosus (SLE) (p<0.001 for the two comparisons). In contrast, those of early Bm5 (eBm5) and Bm5 were decreased in patients with pSS, compared with patients with RA and with SLE (p<0.001 for the two comparisons). The receiver operating characteristic curves allowed for an optimising cut-off value of Bm2+Bm2' cells at 71.1% for 88.0% sensitivity and 83.1% specificity, that of eBm5+Bm5 cells at < or =13.5% for 84.0% sensitivity and 83.1% specificity, and, consequently, that of Bm2+Bm2'/eBm5+Bm5 at > or =5 for 88.0% sensitivity and 84.6% specificity. CONCLUSION: Given its presentation as a signature for pSS, relative to RA and SLE, such a distribution of B-cell subsets might provide a useful diagnostic tool.


Asunto(s)
Subgrupos de Linfocitos B/inmunología , Síndrome de Sjögren/diagnóstico , Adulto , Anciano , Artritis Reumatoide/diagnóstico , Artritis Reumatoide/inmunología , Biomarcadores/sangre , Diagnóstico Diferencial , Método Doble Ciego , Femenino , Humanos , Inmunofenotipificación , Lupus Eritematoso Sistémico/diagnóstico , Lupus Eritematoso Sistémico/inmunología , Masculino , Persona de Mediana Edad , Síndrome de Sjögren/inmunología
4.
Rev Med Interne ; 29(12): 1000-6, 2008 Dec.
Artículo en Francés | MEDLINE | ID: mdl-18403061

RESUMEN

INTRODUCTION: Sjögren's syndrome (SS) is an autoimmune epithelitis hallmarked by a disruption of epithelial cells, the subsequent lymphocytic infiltration of lachrymal and salivary glands (SGs), and their ensuing dryness. One may posit that SS is triggered by viruses, and/or modulated by sex steroid hormones, and there is indeed a consensus that its aetiology is multifactorial, with genetic factors interacting with environmental agents. CURRENT KNOWLEDGE AND KEY POINTS: T-cells have long occupied central stage of the debate on the type of lymphocytes involved in the pathogenesis of SS. The relevance of B cells has, however, been emphasized over the past five years and new insights into their functions revealed. Furthermore, increased levels of the B-cell activating factor (BAFF) may be responsible for quantitative and qualitative anomalies of B-cells found in SS such as emergence of self reactive B-cells. This review reports compelling evidence that B-cells are involved in the pathophysiology of SS. PROSPECTS: Since SS may thus be conceived as a model for B-cell-induced autoimmunity, it is no surprise that B-cell ablative-treatment has proven to be relatively effective in SS.


Asunto(s)
Linfocitos B/fisiología , Síndrome de Sjögren , Animales , Anticuerpos Monoclonales/uso terapéutico , Anticuerpos Monoclonales de Origen Murino , Autoanticuerpos/inmunología , Factor Activador de Células B/inmunología , Receptor del Factor Activador de Células B/inmunología , Linfocitos B/inmunología , Citocinas/inmunología , Citocinas/fisiología , Modelos Animales de Enfermedad , Humanos , Inmunoterapia , Activación de Linfocitos , Linfoma de Células B/etiología , Ratones , Factores de Riesgo , Rituximab , Glándulas Salivales/inmunología , Síndrome de Sjögren/complicaciones , Síndrome de Sjögren/tratamiento farmacológico , Síndrome de Sjögren/etiología , Síndrome de Sjögren/inmunología , Síndrome de Sjögren/fisiopatología , Síndrome de Sjögren/terapia
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