胎儿DNA可能引发Sjögren综合征

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摘要

波兰研究人员声称,不同组织学形式的类风湿性关节炎(RA)可能对治疗有不同的反应,因为它们具有不同的可溶性粘附因子和血管内皮生长因子(VEGF)模式。他们的研究集中在42名RA患者和32名骨关节炎(OA)对照患者的滑膜和血清样本上。RA患者血清可溶性细胞间黏附分子1 (sICAM-1)、可溶性血管黏附分子1 (sVCAM-1)、可溶性e -选择素(sE-selectin)、VEGF浓度均显著高于OA患者。除sE-selectin外,RA患者滤泡性滑膜炎(16)比弥漫性滑膜炎(24)和OA患者高得多。它们还与类风湿关节炎的临床标志物有关,包括红细胞沉降率、C反应蛋白、肿胀关节的数量,以及表明疾病更严重的x光证据。在滤泡性RA中,滑膜在中心核周围含有淋巴细胞的圆形聚集体,并伴有新的毛细血管。在弥漫性滑膜炎和骨性关节炎中,单个核细胞在整个组织中的分布更为均匀。滑膜组织取自髋关节或膝关节手术患者。ELISA法检测血清粘附因子和VEGF浓度。不同类型的滑膜炎似乎与不同模式的细胞因子在滑膜和细胞因子和血清金属蛋白酶。在粘附分子的影响下,巨噬细胞和成纤维细胞向滑膜迁移,VEGF、sVCAM和sE-selectin促进了血管化的增加。细胞因子和金属蛋白酶介导组织破坏,可能由淋巴细胞控制。
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Fetal DNA may spark Sjögren’s syndrome
Distinct histological forms of rheumatoid arthritis (RA) may respond differently to treatment as they have different patterns of soluble adhesion factors and vascular endothelial growth factor (VEGF), Polish researchers claim. Their investigations centred on synovial and serum samples from 42 patients with RA and 32 controls with osteoarthritis (OA). Serum concentrations of soluble intercellular adhesion molecule 1 (sICAM-1), soluble vascular adhesion molecule 1 (sVCAM-1), soluble E-selectin (sE-selectin), and VEGF were significantly higher in patients with RA than OA. All except sE-selectin were much higher for patients with RA showing follicular synovitis (16) compared with patients showing diffuse synovitis (24) and patients with OA. They were also linked with clinical markers for RA, including erythrocyte sedimentation rate, C reactive protein, number of swollen joints, and x ray evidence indicating more severe disease. In follicular RA the synovium contained circular aggregates of lymphocytes around a central core and associated with new capillaries. In diffuse synovitis and OA it showed a more uniform spread of mononuclear cells throughout the tissue. Synovial tissue was taken from patients during hip or knee operations. Serum concentrations of adhesion factors and VEGF were measured by ELISA. Distinct types of synovitis seem to be found with different patterns of cytokines in the synovium and cytokines and metalloproteinases in serum. Macrophages and fibroblasts migrate to the synovium under the influence of adhesion molecules and increased vascularisation promoted by VEGF, sVCAM, and sE-selectin. Once there their cytokines and metalloproteinases mediate tissue destruction, maybe controlled by lymphocytes.
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