期刊论文详细信息
Clinical and Experimental Rheumatology
CD27+ memory and CD27- effector CD8+ T cells are responsible for a decreased production of proinflammatory cytokines in HLA B27-positive subjects
M. Rudwaleit1  J. Sieper1  J. Braun1  S. Kohler1  A. Thiel1 
关键词: TNF-alpha;    IFN-gamma;    HLA B27;    ankylosing spondylitis;    T cells;   
DOI  :  
学科分类:医学(综合)
来源: Pacini Editore SpA
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【 摘 要 】

BACKGROUND AND OBJECTIVES: AS and other spondyloarthritides (SpA) are mostly chronic inflammatory rheumatic diseases characterised by a strong association with HLA B27. Recent data from our group have suggested that AS patients have a diminished secretion capacity of inflammatory cytokines, possibly associated with HLA B27. The aim of this study was to identify CD4+ and CD8+ T cell subsets responsible for the observed lower cytokine secretion capacity in HLA B27-positives. METHODS: Highly purified (> 98%) CD4+ and CD8+ T cells of HLA B27-positive AS patients (n = 13), healthy HLA B27-positive (n = 7) and -negative controls (n = 9) were stimulated for 6h with PMA/ Ionomycin and, after fixation, stained for surface markers CD45RA and CD27 and cytokines TNFα, IFN&ggr;, IL-4 and IL-10. RESULTS: CD27+ CD45RA- memory CD8+ T cells of HLA B27-positive subjects showed a significantly lower percentage of TNFα (median 71.4%) and IFN&ggr; production (median 69.7%) than HLA B27-negative controls (TNFα 85.1%; p ≤ 0.027; IFN&ggr; 82.7%, p ≤ 0.026). A similar result was also detected in CD27- CD45RA+ effector CD8+ T cells of which 43.2% produced TNFα and 66.3% IFN&ggr;in HLA B27-positive subjects, respectively, compared to 75.6% TNFα and 84.4% IFN&ggr;producing T cells in HLA B27-negatives (p ≤ 0.045 and p ≤ 0.062, respectively). For all CD4+ T cell subsets no significant differences between HLA B27-positive and HLA B27-negative donors were observed, regarding neither the frequency of IFN&ggr;, TNFα, IL-4 or IL-10 producers nor the coexpression of IFN&ggr; and IL-4 in memory subsets. CONCLUSIONS: HLA B27-positive subjects are characterized by a low proinflammatory cytokine production in CD8+ effector and memory T cell subsets. This suggests an influence of HLA B27 on cytokine production in antigen-experienced CD8+ T cells.

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