Niimura M
Department of Dermatology, Jikei University School of Medicine, Tokyo, Japan.
J Invest Dermatol. 1990 Dec;95(6 Suppl):149S-151S. doi: 10.1111/1523-1747.ep12875129.
Eighty patients with bilateral common warts of the extremities were treated at weekly intervals with intralesional injections of either human fibroblast interferon or placebo. Lyophilized interferon (3 X 10(6) units) was diluted with 3 ml of normal sterile saline matched with identical vials of placebo. Eighty sets of three vials of human fibroblast interferon or placebo were labeled either A or B by a controller who maintained the code until the experiment was completed. Each patient received 0.1 X 10(6) units of interferon into the warts on one side and placebo injections into those on the matching extremity. Warts were measured each week and the progress or lack thereof was scored on a scale of -1 (worse) to 3 (cured). Therapy continued until either at least one extremity had cleared or the patient had received 10 weekly injections. A final evaluation was scored by measuring the total progress of each patient during the study. Sixty-four patients were treated to completion. More than 81% of the interferon-treated extremities were either cured or responded effectively to therapy. Only 17% of the placebo-treated lesions responded in this fashion. A statistical analysis of these data confirms the effectiveness of intralesional interferon therapy. The average number of interferon injections until cure was 5.9 +/- 1.7. No adverse effects were observed. The applications of interferon in patients with epidermodysplasia verruciformis and flat warts were also studied. Intralesional interferon beta was, to a certain degree, effective for benign lesions of epidermodysplasia verruciformis, but systemic treatments were not effective. Subcutaneous interferon beta was, in an uncontrolled study, effective in 45% of patients with flat warts.
八十例双侧肢体寻常疣患者接受了每周一次的病灶内注射人成纤维细胞干扰素或安慰剂治疗。冻干干扰素(3×10⁶单位)用3毫升与相同安慰剂小瓶匹配的无菌生理盐水稀释。八十组三瓶人成纤维细胞干扰素或安慰剂由一名管理员标记为A或B,该管理员在实验完成前一直保密编码。每位患者一侧的疣体接受0.1×10⁶单位干扰素注射,与之匹配的肢体上的疣体注射安慰剂。每周测量疣体大小,并根据-1(恶化)至3(治愈)的评分标准对进展情况进行评分。治疗持续进行,直到至少一侧肢体疣体清除或患者接受了10次每周注射。通过测量每位患者在研究期间的总体进展情况进行最终评估。六十四例患者完成了治疗。超过81%接受干扰素治疗的肢体疣体治愈或对治疗有有效反应。接受安慰剂治疗的病变中只有17%有此反应。对这些数据的统计分析证实了病灶内注射干扰素治疗的有效性。治愈前干扰素注射的平均次数为5.9±1.7。未观察到不良反应。还研究了干扰素在疣状表皮发育不良和平疣患者中的应用。病灶内注射β干扰素在一定程度上对疣状表皮发育不良的良性病变有效,但全身治疗无效。在一项非对照研究中,皮下注射β干扰素对45%的平疣患者有效。