Edvinsson L I, Edvinsson M L, Angus Deveber G
Department of Internal Medicine, University Hospital of Lund, Lund, Sweden.
Int Angiol. 2003 Jun;22(2):141-7.
Vasogen's immune modulation therapy (IMT)* involves the ex vivo exposure of a sample of autologous blood to 3 oxidative stress factors (heat, an oxidative environment, and ultraviolet light), followed by intramuscular re-injection. The primary objective of this study was to assess the effect of Vasogen's IMT on skin blood flow in patients with symptomatic peripheral arterial occlusive disease (PAOD).
In a double-blind, placebo-controlled pilot study, 18 patients with moderately advanced PAOD were randomized to receive 2 courses each of 6 intramuscular injections of either saline or Vasogen's IMT over a 9-week period. Dorsal foot skin blood flow was assessed directly using laser Doppler fluxmetry (LDF) and indirectly using measurement of transcutaneous pO(2) (tcpO(2)). Key outcome measures of skin blood flow were, for LDF: resting values, peak postischemic values, and the total time to reach peak values following release from 4 min of total foot ischemia and, for tcpO(2): resting values and the time for tcpO(2) to reach 50% of the pre-ischemia value. Measurements were carried out at baseline, at weeks 3, 6, and 9, and at 2 months post-therapy.
No significant differences were detected between groups for resting or peak postischemic LDF values for dorsal foot skin blood flow. Patients randomised to IMT experienced a progressive decrease in the time to peak postischemic skin blood flow, reaching statistical significance at 2 months. Treated patients experienced a 26.1 s decrease in time to peak blood flow (p=0.026) vs a 7.9 s decrease in the placebo group (p=ns). Similar but less striking results were achieved for tcpO(2) recovery time to 50% of pre-ischemia values (treated group, p=0.035; placebo group, p=ns).
Vasogen's IMT improved recovery rates of postischemic dorsal foot skin blood flow in a group of patients with moderately advanced PAOD, probably due to improved endothelial function.
Vasogen公司的免疫调节疗法(IMT)*包括将自体血样本在体外暴露于3种氧化应激因素(热、氧化环境和紫外线),然后进行肌肉内再次注射。本研究的主要目的是评估Vasogen公司的IMT对有症状的外周动脉闭塞性疾病(PAOD)患者皮肤血流的影响。
在一项双盲、安慰剂对照的初步研究中,18例中度晚期PAOD患者被随机分组,在9周内接受6次肌肉注射生理盐水或Vasogen公司的IMT,各2个疗程。使用激光多普勒血流仪(LDF)直接评估足背皮肤血流,使用经皮氧分压(tcpO₂)测量间接评估。皮肤血流的关键结局指标,对于LDF:静息值、缺血后峰值以及从足总缺血4分钟后释放至达到峰值的总时间,对于tcpO₂:静息值以及tcpO₂达到缺血前值50%的时间。在基线、第3、6和9周以及治疗后2个月进行测量。
两组足背皮肤血流的静息或缺血后峰值LDF值未检测到显著差异。随机接受IMT的患者缺血后皮肤血流达到峰值的时间逐渐减少,在2个月时达到统计学显著性。治疗组患者血流达到峰值的时间减少了26.1秒(p = 0.026),而安慰剂组减少了7.9秒(p =无统计学意义)。对于tcpO₂恢复到缺血前值50%的时间,结果相似但不太显著(治疗组,p = 0.035;安慰剂组,p =无统计学意义)。
Vasogen公司的IMT改善了一组中度晚期PAOD患者缺血后足背皮肤血流的恢复率,可能是由于内皮功能改善。