Your browser doesn't support javascript.
loading
CP-690550 Treatment Ameliorates Established Disease and Provides Long-Term Therapeutic Effects in an SKG Arthritis Model
Immune Network ; : 257-263, 2013.
Artigo em Inglês | WPRIM | ID: wpr-83832
ABSTRACT
Although pathogenesis of human rheumatoid arthritis (RA) remains unclear, arthritogenic T cells and downstream signaling mediators have been shown to play critical roles. An increasing numbers of therapeutic options have been added for the effective control of RA. Nevertheless, there is still a category of patients that fails treatment and suffers from progressive disease. The recently developed immunosuppressant CP-690550, a small molecule JAK kinase inhibitor, has been implicated as an important candidate treatment modality for autoimmune arthritis. In this study, we evaluated the therapeutic effect of CP-690550 on established arthritis using an SKG arthritis model, a pathophysiologically relevant animal model for human RA. CP-690550 treatment revealed remarkable long-term suppressive effects on SKG arthritis when administered to the well-advanced disease (clinical score 3.5~4.0). The treatment effect lasted at least 3 more weeks after cessation of drug infusion, and suppression of disease was correlated with the reduced pro-inflammatory cytokines, including IL-17, IFN-gamma, and IL-6 and increased level of immunoregulatory IL-10.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Fosfotransferases / Artrite / Artrite Reumatoide / Linfócitos T / Citocinas / Interleucina-6 / Interleucina-10 / Interleucina-17 / Modelos Animais Tipo de estudo: Estudo prognóstico Limite: Humanos Idioma: Inglês Revista: Immune Network Ano de publicação: 2013 Tipo de documento: Artigo

Similares

MEDLINE

...
LILACS

LIS

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Fosfotransferases / Artrite / Artrite Reumatoide / Linfócitos T / Citocinas / Interleucina-6 / Interleucina-10 / Interleucina-17 / Modelos Animais Tipo de estudo: Estudo prognóstico Limite: Humanos Idioma: Inglês Revista: Immune Network Ano de publicação: 2013 Tipo de documento: Artigo