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重组干扰素-γ(rIFN-γ)用于特应性皮炎的长期治疗。

Long-term therapy with recombinant interferon-gamma (rIFN-gamma) for atopic dermatitis.

作者信息

Schneider L C, Baz Z, Zarcone C, Zurakowski D

机构信息

Division of Immunology, Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.

出版信息

Ann Allergy Asthma Immunol. 1998 Mar;80(3):263-8. doi: 10.1016/S1081-1206(10)62968-7.

Abstract

BACKGROUND

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.

OBJECTIVE

We evaluated the safety and efficacy of long-term use of rIFN-gamma for severe atopic dermatitis.

METHODS

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.

RESULTS

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.

CONCLUSIONS

We conclude that rIFN-gamma appears to be a safe long-term therapy for patients with severe atopic dermatitis.

摘要

背景

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。

目的

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。

方法

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。

结果

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。

结论

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。

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