Baeten D, Houbiers J, Kruithof E, Vandooren B, Van den Bosch F, Boots A M, Veys E M, Miltenburg A M M, De Keyser F
Clinical Immunology and Rheumatology, Academic Medical Centre University of Amsterdam, Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands.
Ann Rheum Dis. 2006 Aug;65(8):990-7. doi: 10.1136/ard.2005.047852. Epub 2006 Jan 13.
To determine the impact on synovial histopathology of changes in clinical disease activity in the absence of effective treatment.
Twelve patients with active RA not receiving effective treatment were studied over a 14 week period. Synovial biopsy specimens obtained at baseline and week 14 were analysed by histology and immunohistochemistry.
Over the course of 14 weeks, there was a trend towards a decrease of the DAS28, with 7/12 patients being good or moderate DAS28 responders despite the absence of effective treatment. Patients' assessment of global disease activity and swollen joint count both decreased significantly. Histologically, there was a decrease of lining layer hyperplasia and lymphoid aggregates, a similar trend for vascularity, but there was no effect on global synovial infiltration. Accordingly, there was no decrease of the cellular infiltration with T lymphocytes (CD3, CD4, CD8), B lymphocytes (CD20), plasma cells (CD38), dendritic cells (CD1a, CD83), and even an increase of CD163+ sublining macrophages, with a similar trend for CD68+ sublining macrophages. The changes in DAS28 scores in these patients did not correlate with changes in histological variables, with the exception of an inverse correlation with plasma cells. Remarkably, even in the DAS28 responders, no significant changes in synovial inflammatory infiltration were noted.
Despite variations in global disease activity, synovial inflammatory infiltration did not change significantly in the absence of effective treatment. The lack of a placebo effect on synovial markers of treatment response such as sublining macrophages can facilitate conclusive early phase trials with small numbers of patients with RA.
确定在未进行有效治疗的情况下,临床疾病活动度变化对滑膜组织病理学的影响。
对12例未接受有效治疗的活动性类风湿关节炎患者进行了为期14周的研究。对基线和第14周时获取的滑膜活检标本进行组织学和免疫组织化学分析。
在14周的过程中,疾病活动度评分(DAS28)有下降趋势,尽管未进行有效治疗,但12例患者中有7例为DAS28良好或中度反应者。患者对整体疾病活动度的评估以及肿胀关节计数均显著下降。组织学上,衬里层增生和淋巴样聚集减少,血管形成有类似趋势,但对整体滑膜浸润无影响。因此,T淋巴细胞(CD3、CD4、CD8)、B淋巴细胞(CD20)、浆细胞(CD38)、树突状细胞(CD1a、CD83)的细胞浸润没有减少,甚至CD163 + 衬里下层巨噬细胞增加,CD68 + 衬里下层巨噬细胞有类似趋势。这些患者的DAS28评分变化与组织学变量的变化无关,浆细胞情况除外。值得注意的是,即使在DAS28反应者中,也未观察到滑膜炎症浸润有显著变化。
尽管整体疾病活动度存在差异,但在未进行有效治疗的情况下,滑膜炎症浸润没有显著变化。对治疗反应的滑膜标志物如衬里下层巨噬细胞缺乏安慰剂效应,有助于对少量类风湿关节炎患者进行确定性的早期试验。