Rieckmann P, Altenhofen B, Riegel A, Kallmann B, Felgenhauer K
Department of Neurology, University of Würzburg, Germany.
Mult Scler. 1998 Jun;4(3):178-82. doi: 10.1177/135245859800400317.
Several studies have reported a positive correlation between levels of soluble adhesion molecules in serum or cerebrospinal fluid and cranial MRI activity. We performed a cross-sectional study in 46 patients with newly diagnosed MS and determined levels of soluble intercellular adhesion molecule-I (sICAM-I) as well as vascular cell adhesion molecule-I (sVCAM-I) in correlation to the number and area of gadolinium enhancing lesions on cranial magnetic resonance images (MRI). The data revealed a significant positive correlation between sVCAM-I serum levels and gadolinium enhancing lesions. In addition, CSF to serum ratios for sICAM-I and sVCAM-I correlated to MRI activity. In patients with a single enhancing lesion (SEL) there was a negative correlation between the QsCAM and the distance of the SEL to the ventricles. As these adhesion molecules are stable and markers of disease activity in MS, we further investigated sVCAM-I serum levels during treatment with interferon beta-Ib (Betaferon). Significant increases in serum levels for sVCAM-I in patients receiving Betaferon were associated with a favourable treatment response after 1 year in 17 out of 19 patients and correlated to decreased MRI activity, whereas stable or reduced sVCAM-I levels occurred more often in non-responders (five out of six patients). Therefore it can be hypothesized that soluble adhesion molecules are released from cerebral endothelial cells as an early immunoregulatory activity of the immune system to reduce cellular traffic across the blood brain barrier and this is further enhanced by IFN-beta treatment.
多项研究报告称,血清或脑脊液中可溶性黏附分子水平与头颅MRI活性之间存在正相关。我们对46例新诊断的多发性硬化症患者进行了一项横断面研究,测定了可溶性细胞间黏附分子-1(sICAM-1)以及血管细胞黏附分子-1(sVCAM-1)的水平,并将其与头颅磁共振成像(MRI)上钆增强病灶的数量和面积进行关联分析。数据显示,sVCAM-1血清水平与钆增强病灶之间存在显著正相关。此外,sICAM-1和sVCAM-1的脑脊液与血清比值与MRI活性相关。在仅有一个增强病灶(SEL)的患者中,QsCAM与SEL到脑室的距离之间存在负相关。由于这些黏附分子在多发性硬化症中是稳定的且是疾病活动的标志物,我们进一步研究了用干扰素β-1b(β干扰素)治疗期间sVCAM-1的血清水平。接受β干扰素治疗的患者中,sVCAM-1血清水平显著升高与19例患者中的17例在1年后的良好治疗反应相关,且与MRI活性降低相关,而在无反应者中(6例患者中的5例),sVCAM-1水平稳定或降低更为常见。因此,可以推测可溶性黏附分子是作为免疫系统的一种早期免疫调节活性从脑内皮细胞释放出来的,以减少细胞穿越血脑屏障的流量,并且干扰素β治疗可进一步增强这种作用。