Suppr超能文献

一项针对10名常见可变免疫缺陷(CVID)患者的双盲、安慰剂对照、交叉治疗研究,该研究使用天然人白细胞介素-2(nhuIL-2)联合常规静脉注射丙种球蛋白(IVIG)。

A double-blind, placebo-controlled, crossover therapy study with natural human IL-2 (nhuIL-2) in combination with regular intravenous gammaglobulin (IVIG) infusions in 10 patients with common variable immunodeficiency (CVID).

作者信息

Rump J A, Jahreis A, Schlesier M, Stecher S, Peter H H

机构信息

Department of Medicine, University Hospital, Freiburg, Germany.

出版信息

Clin Exp Immunol. 1997 Nov;110(2):167-73. doi: 10.1111/j.1365-2249.1997.tb08313.x.

Abstract

Ten CVID patients with defective IL-2 synthesis in vitro were treated with nhuIL-2 in a placebo-controlled, double blind, crossover therapy study during a period of 12 months. No severe side-effects of nhuIL-2 were recorded. Marginal serum nhuIL-2 levels were measurable in individual patients only during the therapy phase. Serum levels of soluble IL-2 receptors were unaffected by the therapy. nhuIL-2 and placebo groups did not differ significantly with respect to requirement of IVIG substitutions which were performed whenever serum IgG levels dropped below 5 g/l: a total of 53 IVIG infusions (corresponding to 17.6 g IgG/month per patient) was necessary during the placebo phase, and 48 infusions (16.4 g IgG/month per patient) during the nhuIL-2 treatment phase. Thus, nhuIL-2 therapy was ineffective in improving spontaneous IgG synthesis in vivo. Nevertheless, the group of patients receiving nhuIL-2 during the first 6 months of the study exhibited a significant reduction of severe infections (n = 25) during the following 6 months of placebo treatment (n = 7) (P<0.045). The infection score dropped in this group from 181 to 23 (P<0.015). Patients of the second group receiving first placebo and then nhuIL-2 did not experience a significant difference in number and score of infectious episodes: 25 infections were recorded during the first 6 months and 24 during the following 6 months. We suppose that nhuIL-2 therapy of CVID patients reduces susceptibility to severe infections, possibly via the induction of a specific antibody response, which is effective at the earliest 6 months after initiating nhuIL-2 therapy.

摘要

在一项为期12个月的安慰剂对照、双盲、交叉治疗研究中,对10名体外白细胞介素-2(IL-2)合成有缺陷的常见变异型免疫缺陷病(CVID)患者使用重组人IL-2(nhuIL-2)进行治疗。未记录到nhuIL-2的严重副作用。仅在治疗阶段个别患者中可检测到微量血清nhuIL-2水平。治疗对血清可溶性IL-2受体水平无影响。nhuIL-2组和安慰剂组在静脉注射免疫球蛋白(IVIG)替代需求方面无显著差异,只要血清免疫球蛋白G(IgG)水平降至5 g/l以下就进行IVIG替代:在安慰剂阶段共需要53次IVIG输注(相当于每位患者每月17.6 g IgG),在nhuIL-2治疗阶段需要48次输注(每位患者每月16.4 g IgG)。因此,nhuIL-2治疗在改善体内自发IgG合成方面无效。然而,在研究的前6个月接受nhuIL-2治疗的患者组在随后6个月的安慰剂治疗期间严重感染(n = 25)显著减少(n = 7)(P<0.045)。该组感染评分从181降至23(P<0.015)。第二组患者先接受安慰剂治疗,然后接受nhuIL-2治疗,在感染发作的数量和评分上没有显著差异:在前6个月记录到25次感染,在随后6个月记录到24次感染。我们推测,CVID患者的nhuIL-2治疗可能通过诱导特异性抗体反应降低对严重感染的易感性,这种反应最早在开始nhuIL-2治疗6个月后才有效。

相似文献

本文引用的文献

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验