Baeten D, Demetter P, Cuvelier C, Van Den Bosch F, Kruithof E, Van Damme N, Verbruggen G, Mielants H, Veys E M, De Keyser F
Department of Rheumatology, University Hospital, University of Ghent, Belgium.
Ann Rheum Dis. 2000 Dec;59(12):945-53. doi: 10.1136/ard.59.12.945.
To compare the macroscopic and microscopic characteristics of synovial tissue in rheumatoid arthritis (RA), spondyloarthropathy (SpA), and osteoarthritis (OA) after exclusion of possible biases induced by disease duration or activity, or both.
Synovial biopsy specimens were obtained by needle arthroscopy in patients with early RA (n=16), late RA (n=14), early SpA (n=23), and OA (n=12). Macroscopic and microscopic features were scored on a four point scale and analysed as a function of disease duration (early versus late RA), local and systemic disease activity, and diagnosis.
Except for the maximal synovial lining thickness, no significant differences were seen between early and late RA. For disease activity, synovial histology was only weakly correlated with C reactive protein in RA, but seemed to be strongly dependent on effusion of the biopsied joint in all disease groups. After stratification for local disease activity, no disease related differences were found in patients without joint effusion. In contrast, important differences were found between patients with RA and SpA with active joint effusion. Synovial vascularity was macroscopically increased in SpA versus RA (p=0.017). A straight vessel pattern was only seen in RA, while tortuous vessels were preferentially seen in SpA. Vascularity was also microscopically increased in SpA compared with RA (p=0.031), and correlated with the macroscopic vascularity (r(s)=0.36, p=0.036). CD3+ (p=0.008), CD4+ (p=0.008), and CD20+ (p=0.024) lymphocytes were overrepresented in RA compared with SpA. The integrin expression in RA was characterised by a decrease of alphaVbeta3 in the synovial lining (p=0.006) and an increase of alphaVbeta5 in the sublining (p<0.001).
The immune architecture of the synovial membrane is more dependent on local disease activity than on disease duration. Synovium obtained from clinically affected joints shows important histological differences between RA and SpA.
排除疾病持续时间或活动度或两者所导致的可能偏差后,比较类风湿关节炎(RA)、脊柱关节炎(SpA)和骨关节炎(OA)滑膜组织的宏观和微观特征。
通过针式关节镜检查获取早期RA患者(n = 16)、晚期RA患者(n = 14)、早期SpA患者(n = 23)和OA患者(n = 12)的滑膜活检标本。对宏观和微观特征进行四分制评分,并作为疾病持续时间(早期与晚期RA)、局部和全身疾病活动度以及诊断的函数进行分析。
除滑膜衬里最大厚度外,早期和晚期RA之间未见显著差异。对于疾病活动度,滑膜组织学在RA中仅与C反应蛋白呈弱相关,但在所有疾病组中似乎强烈依赖于活检关节的积液情况。在对局部疾病活动度进行分层后,无关节积液的患者中未发现与疾病相关的差异。相反,有活动性关节积液的RA和SpA患者之间发现了重要差异。与RA相比,SpA的滑膜血管在宏观上增加(p = 0.017)。直线血管模式仅在RA中可见,而迂曲血管在SpA中更常见。与RA相比,SpA的血管在微观上也增加(p = 0.031),并且与宏观血管性相关(r(s)=0.36,p = 0.036)。与SpA相比,RA中CD3 +(p = 0.008)、CD4 +(p = 0.008)和CD20 +(p = 0.024)淋巴细胞的比例过高。RA中的整合素表达特征为滑膜衬里中αVβ3减少(p = 0.006),滑膜下层中αVβ5增加(p < 0.001)。
滑膜的免疫结构更多地依赖于局部疾病活动度而非疾病持续时间。从临床受累关节获取的滑膜在RA和SpA之间显示出重要的组织学差异。