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Arthritis Rheum ; 50(4): 1164-71, 2004 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-15077298

RESUMO

OBJECTIVE: The stress protein and endoplasmic reticulum chaperone, immunoglobulin binding protein (BiP), is an autoantigen in rheumatoid arthritis (RA). Stress proteins, however, may have extracellular functions, mediated via cell surface receptors, that may include immunomodulatory functions. We sought to determine whether cell-free BiP is present in the synovial fluid (SF) of patients with RA and to further investigate the possible extracellular antiinflammatory and immunomodulatory properties of BiP in peripheral blood mononuclear cells (PBMCs) in vitro. METHODS: The presence of BiP in SF was established by Western blotting. PBMCs were stimulated with exogenous recombinant human BiP, and cytokine production and cell proliferation were measured in the presence and absence of cell signaling inhibitors or neutralizing anti-interleukin-10 (anti-IL-10) monoclonal antibody. Cytokine levels were quantified by enzyme-linked immunosorbent assay, cell proliferation by tritiated thymidine uptake, and cell surface molecule expression by flow cytometry. RESULTS: PBMCs responded to BiP with secretion of an antiinflammatory profile of cytokines. Although BiP stimulated the early production of tumor necrosis factor alpha (TNF alpha), the major cytokine induced was IL-10. Soluble TNF receptor II and IL-1 receptor antagonist secretion was also increased. Addition of SB203580, the MAPK p38 pathway inhibitor, partially inhibited the production of IL-10 and TNF alpha, whereas they were unaffected by the MAPK ERK-1/2 inhibitor PD98059. BiP also inhibited the recall antigen response by PBMCs to tuberculin purified protein derivative. Further investigation showed that incubation of monocytes in the presence of either BiP or IL-10 down-regulated CD86 and HLA-DR expression. The effect observed with IL-10 was transient compared with the long-lasting reduction induced by BiP. CONCLUSION: Extracellular BiP may stimulate immunomodulatory and antiinflammatory pathways, which are only partly due to the production of IL-10. These properties may be of relevance for the treatment of diseases such as RA.


Assuntos
Células Apresentadoras de Antígenos/imunologia , Artrite Reumatoide/imunologia , Proteínas de Transporte/metabolismo , Proteínas de Choque Térmico , Interleucina-10/metabolismo , Chaperonas Moleculares/metabolismo , Monócitos/imunologia , Fator de Necrose Tumoral alfa/metabolismo , Células Apresentadoras de Antígenos/metabolismo , Antígenos CD/metabolismo , Artrite Reumatoide/metabolismo , Antígeno B7-2 , Células Cultivadas , Regulação para Baixo/imunologia , Chaperona BiP do Retículo Endoplasmático , Espaço Extracelular/metabolismo , Antígenos HLA-DR/metabolismo , Humanos , Técnicas In Vitro , Proteína Antagonista do Receptor de Interleucina 1 , Interleucina-1/metabolismo , Sistema de Sinalização das MAP Quinases/imunologia , Glicoproteínas de Membrana/metabolismo , Monócitos/metabolismo , Receptores do Fator de Necrose Tumoral/metabolismo , Receptores Tipo II do Fator de Necrose Tumoral , Sialoglicoproteínas/metabolismo , Líquido Sinovial/imunologia , Líquido Sinovial/metabolismo , Tuberculina/farmacologia
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