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Relationship between CD5+ B lymphocytes and the activity of systemic autoimmunity.
Becker, H; Weber, C; Storch, S; Federlin, K.
Afiliação
  • Becker H; III. Medizinische Klinik und Poliklinik, Universität Giessen, Federal Republic of Germany.
Clin Immunol Immunopathol ; 56(2): 219-25, 1990 Aug.
Article em En | MEDLINE | ID: mdl-1696188
ABSTRACT
We studied the relationship between CD5+ B cells and the activity of the disease process in patients with autoimmune diseases. In rheumatoid arthritis (RA), levels of CD5+ B cells were associated with autoantibody production as determined by serum rheumatoid factor and antinuclear antibodies. In addition, CD5+ B cells were significantly correlated with C-reactive protein, and data from longitudinal studies showed a marked influence of corticosteroid treatment on numbers of CD5+ B cells. Patients with systemic lupus erythematosus (SLE) had slightly elevated levels of CD5+ B cells as compared with normals, but a close association with measures of an active disease was not observed. In a group of patients with type I diabetes mellitus, CD5+ B cells were detected in patients with anti-islet cell antibodies. Our results suggest that CD5+ B cells are related to the activity of the autoimmune process and can be modulated by therapy in patients with RA. Although CD5+ B cells do not seem to have a major role in SLE, polyclonal activation might affect this B cell subset as well in this disease. Further studies are needed to define the precise role of CD5+ B cells in organ-specific autoimmunity.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfócitos B / Antígenos de Diferenciação / Autoimunidade Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Clin Immunol Immunopathol Ano de publicação: 1990 Tipo de documento: Article
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfócitos B / Antígenos de Diferenciação / Autoimunidade Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Clin Immunol Immunopathol Ano de publicação: 1990 Tipo de documento: Article