Schneider L C, Baz Z, Zarcone C, Zurakowski D
Division of Immunology, Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Ann Allergy Asthma Immunol. 1998 Mar;80(3):263-8. doi: 10.1016/S1081-1206(10)62968-7.
Interferon-gamma (IFN-gamma) is a potent cytokine that modulates IL-4-induced immune responses. Atopic dermatitis is associated with increased IgE levels and decreased IFN-gamma production. Recent phase I and phase II studies have suggested that short-term rIFN-gamma therapy is effective in the treatment of severe atopic dermatitis.
We evaluated the safety and efficacy of long-term use of rIFN-gamma for severe atopic dermatitis.
Fifteen patients were treated for a minimum of 22 months with 50 micrograms/m2 rIFN-gamma qd or qod. Patients were monitored every 3 months for safety, efficacy, and linear growth in pediatric patients.
Data represented a total of 47 patient years, which included 29 pediatric patient years. There was a statistically significant decrease in mean total body surface area involvement over time (P < .001, ANOVA). Mean total body surface area involvement was 61.6% at baseline and decreased to 18.5% at 24 months (P < .001). Likewise, there was a statistically significant decrease in the clinical severity parameters. The mean total clinical severity score was 11.4 at baseline and decreased to 6.3 at 24 months (P < .001). Statistically significant decreases in WBC, neutrophil counts, and eosinophil counts were observed compared with baseline counts. No other significant laboratory abnormalities or growth problems were seen.
We conclude that rIFN-gamma appears to be a safe long-term therapy for patients with severe atopic dermatitis.
干扰素-γ(IFN-γ)是一种强效细胞因子,可调节白细胞介素-4诱导的免疫反应。特应性皮炎与免疫球蛋白E水平升高和干扰素-γ产生减少有关。近期的I期和II期研究表明,短期重组干扰素-γ治疗对重度特应性皮炎有效。
我们评估了长期使用重组干扰素-γ治疗重度特应性皮炎的安全性和有效性。
15例患者接受50微克/平方米重组干扰素-γ每日一次或隔日一次治疗,最短治疗22个月。每3个月对患者进行安全性、有效性监测,并监测儿科患者的线性生长情况。
数据总计47患者年,其中包括29儿科患者年。随着时间的推移,平均全身表面积受累情况有统计学显著下降(P <.001,方差分析)。基线时平均全身表面积受累为61.6%,24个月时降至18.5%(P <.001)。同样,临床严重程度参数也有统计学显著下降。平均总临床严重程度评分基线时为11.4,24个月时降至6.3(P <.001)。与基线计数相比,白细胞、中性粒细胞计数和嗜酸性粒细胞计数有统计学显著下降。未观察到其他显著的实验室异常或生长问题。
我们得出结论,重组干扰素-γ似乎是重度特应性皮炎患者安全的长期治疗方法。