Kruithof E, Baeten D, Van den Bosch F, Mielants H, Veys E M, De Keyser F
Department of Rheumatology, Ghent University Hospital, De Pintelaan 185, 9000 Gent, Belgium.
Ann Rheum Dis. 2005 Apr;64(4):529-36. doi: 10.1136/ard.2003.018549. Epub 2004 Sep 23.
To confirm and extend the immunopathological evidence of effects of infliximab on the synovium in active spondyloarthropathy.
Synovial biopsies obtained in patients with spondyloarthropathy at baseline and week 12 were stained and scored by two independent observers. Two study populations were evaluated: I, a cohort of 10 patients treated with 5 mg/kg infliximab at week 0, 2, and 6, plus three placebo treated patients; and II, a pooled cohort of 20 patients fulfilling identical inclusion and exclusion criteria and treated with the same loading dose regimen.
In study population I, treatment with infliximab induced reduction in synovial lining layer thickness (p = 0.015), endothelial activation (E-selectin, p = 0.034), and inflammatory cell infiltration with neutrophils (p = 0.041), macrophages (p = 0.034), and T cells (p = 0.026), but not with B cells and plasma cells; no such trends were observed in the placebo treated patients. Besides confirming the highly significant downregulation of inflammation, analysis of cohort II showed structural changes such as normalisation of lining layer thickness (p = 0.030), reduction in the number of blood vessels (p = 0.039), and downregulation of follicular organisation (p = 0.050). No differences in histopathological response were observed between spondyloarthropathy subtypes.
Profound immunomodulatory changes in the synovium parallel the clinical benefit in patients with spondyloarthropathy treated with infliximab, independently of the subtype. The study provides histological evidence that TNF alpha blockade not only downregulates inflammation but also leads to tissue remodelling.
证实并拓展英夫利昔单抗对活动期脊柱关节病滑膜影响的免疫病理学证据。
由两名独立观察者对脊柱关节病患者在基线期和第12周获取的滑膜活检组织进行染色和评分。评估了两个研究人群:I,一组10例患者,在第0、2和6周接受5 mg/kg英夫利昔单抗治疗,外加3例接受安慰剂治疗的患者;II,一组20例患者的汇总队列,这些患者符合相同的纳入和排除标准,并接受相同的负荷剂量方案治疗。
在研究人群I中,英夫利昔单抗治疗导致滑膜衬里层厚度降低(p = 0.015)、内皮细胞活化(E-选择素,p = 0.034)以及中性粒细胞(p = 0.041)、巨噬细胞(p = 0.034)和T细胞(p = 0.026)的炎性细胞浸润减少,但B细胞和浆细胞未减少;在接受安慰剂治疗的患者中未观察到此类趋势。除了证实炎症的高度显著下调外,对队列II的分析显示了结构变化,如衬里层厚度正常化(p = 0.030)、血管数量减少(p = 0.039)以及滤泡组织下调(p = 0.050)。在脊柱关节病亚型之间未观察到组织病理学反应的差异。
在用英夫利昔单抗治疗的脊柱关节病患者中,滑膜的深刻免疫调节变化与临床益处平行,且与亚型无关。该研究提供了组织学证据,表明肿瘤坏死因子α阻断不仅下调炎症,还导致组织重塑。