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T-regulatory cells in systemic lupus erythematosus.
La Cava, A.
Afiliación
  • La Cava A; Division of Rheumatology, Department of Medicine, University of California Los Angeles, Los Angeles, California 90095-1670, USA. alacava@mednet.ucla.edu
Lupus ; 17(5): 421-5, 2008 May.
Article en En | MEDLINE | ID: mdl-18490420
Thymus-derived CD4(+)CD25(high)Foxp3(+) T-regulatory cells (Tregs) have an important role in the mechanisms of peripheral immune tolerance and in the prevention of pathogenic autoimmunity through the suppression of proliferation and production of pro-inflammatory cytokines in effector immune cells. Some studies have shown that in systemic lupus erythematosus (SLE) the number of circulating Tregs may be decreased during active disease, and that the extent of such decrease may correlate with severity of the disease. Recent data in murine models of lupus have suggested the possibility to target Tregs for the modulation of SLE, and Treg-based intervention has been proposed as a novel therapeutic mean for a better management of the disease. This review provides an update on the role of Tregs in SLE, discussing new findings in relation to possible targeting of Tregs for immune modulation in lupus.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Linfocitos T Reguladores / Lupus Eritematoso Sistémico Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Lupus Asunto de la revista: REUMATOLOGIA Año: 2008 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Linfocitos T Reguladores / Lupus Eritematoso Sistémico Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Lupus Asunto de la revista: REUMATOLOGIA Año: 2008 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido