Ulfgren A K, Andersson U, Engström M, Klareskog L, Maini R N, Taylor P C
Karolinska Hospital, Stockholm, Sweden.
Arthritis Rheum. 2000 Nov;43(11):2391-6. doi: 10.1002/1529-0131(200011)43:11<2391::AID-ANR3>3.0.CO;2-F.
To investigate the hypothesis that tumor necrosis factor alpha (TNFalpha) blockade in rheumatoid arthritis (RA) diminishes synovial synthesis of TNFalpha, interleukin-1alpha (IL-1alpha), and IL-1beta.
Patients with active RA received a single 10 mg/kg infusion of infliximab. Multiple synovial biopsy specimens were obtained from a knee the day before infusion and 14 days later. A modified immunohistochemical method detecting cytokine-producing rather than cytokine-binding cells was applied to determine synthesis of TNFalpha, IL-1alpha, and IL-1beta in fixed, cryopreserved sections. Computerized image analysis using two different methodologies was performed by independent observers blinded to the identity of samples.
All 8 patients met the American College of Rheumatology 20% improvement response criteria (ACR 20) at 2 weeks, and half of these patients met the ACR 50. With a few exceptions, there was concordance between both image analysis methodologies regarding the direction of change in immunopositive area fraction for all cytokines analyzed. TNFalpha synthesis was significantly reduced after treatment (P = 0.05 at the Karolinska Institute, Stockholm, Sweden; P = 0.008 at the Kennedy Institute, London, UK). Patients meeting the ACR 50 were those with the highest baseline levels of TNFalpha synthesis. There was a significant correlation between baseline levels of TNFalpha expression and change in TNFalpha levels in response to therapy. Both IL-1alpha and IL-1beta synthesis were reduced in 3 patients; IL-1alpha synthesis alone was reduced in 2 patients and IL-1beta synthesis alone was reduced in 2 patients. In 1 patient, neither IL-1alpha nor IL-1beta synthesis was reduced.
Analysis of synovial tissue by means of immunomorphology and image analysis in a clinical trial setting may allow the drawing of biologically meaningful conclusions. Synovial TNFalpha synthesis was reduced 2 weeks after infliximab treatment. Reductions in IL-1alpha and IL-1beta synthesis were demonstrated in a subgroup of patients. High levels of synovial TNFalpha production prior to treatment may predict responsiveness to therapy.
探讨类风湿关节炎(RA)中肿瘤坏死因子α(TNFα)阻断可减少滑膜中TNFα、白细胞介素-1α(IL-1α)和白细胞介素-1β(IL-1β)合成这一假说。
活动性RA患者接受单次10mg/kg英夫利昔单抗输注。在输注前一天和14天后从膝关节获取多个滑膜活检标本。应用一种改良的免疫组织化学方法检测产生细胞因子而非结合细胞因子的细胞,以确定固定、冷冻保存切片中TNFα、IL-1α和IL-1β的合成。由对样本身份不知情的独立观察者采用两种不同方法进行计算机图像分析。
所有8例患者在2周时均达到美国风湿病学会20%改善反应标准(ACR 20),其中一半患者达到ACR 50。除少数例外,两种图像分析方法在所有分析细胞因子的免疫阳性面积分数变化方向上具有一致性。治疗后TNFα合成显著降低(瑞典斯德哥尔摩卡罗林斯卡学院P = 0.05;英国伦敦肯尼迪学院P = 0.008)。达到ACR 50的患者是TNFα合成基线水平最高的患者。TNFα表达基线水平与治疗后TNFα水平变化之间存在显著相关性。3例患者的IL-1α和IL-1β合成均降低;仅2例患者的IL-1α合成降低,仅2例患者的IL-1β合成降低。1例患者的IL-1α和IL-1β合成均未降低。
在临床试验环境中通过免疫形态学和图像分析对滑膜组织进行分析可能有助于得出具有生物学意义的结论。英夫利昔单抗治疗2周后滑膜TNFα合成降低。在部分患者亚组中证实了IL-1α和IL-1β合成降低。治疗前高水平的滑膜TNFα产生可能预测对治疗的反应性。