ALLERGY Net: Effectiveness of omalizumab in monozygotic twin sisters with severe allergic asthma

医学 奥马佐单抗 哮喘 儿科 安慰剂 一致性 过敏 氟替卡松 单卵双胞胎 人口 过敏性 免疫学 内科学 免疫球蛋白E 抗体 病理 替代医学 环境卫生 生物 遗传学
作者
J. Just,F. Sahraoui,Vincent Gros,A Grimfeld
出处
期刊:Allergy [Wiley]
卷期号:62 (4): 453-454 被引量:2
标识
DOI:10.1111/j.1398-9995.2006.01314.x
摘要

Between 5% and 10% of children worldwide suffer from asthma (1). The familial nature of asthma is well known; the risk for a first cousin of an asthmatic patient is multiplied by 2.5–3 compared with the general population (2). Studies of twins have confirmed this genetic component finding higher concordance of asthma among monozygotic (58.97%) than dizygotic twins (23.64%) (3). We report an exceptional clinical situation of monozygotic twin sisters with severe allergic asthma where one was treated with a monoclonal anti-IgE antibody (omalizumab), and the other with a placebo in a randomized, double-blind, placebo-controlled study (4). Premature monozygotic twin sisters developed bronchopulmonary dysplasia secondary to hyaline membrane disease. Afterwards, the two sisters had similar respiratory history; first, asthma with exacerbations related to viral infections in infancy, then at the age of 6, developing respiratory allergies to various aeroallergens with symptoms of seasonal rhinitis and persistent atopic dermatitis. Despite treatment with high doses of inhaled corticosteroids in combination with long-acting β2-mimetics and delayed-release theophylline, their asthma remained poorly controlled. Repeated severe exacerbations (>10 hospitalizations between 4 and 8) led to several stays in the mountains for climatic treatment. In 1998 at the age of 12, the twins were enrolled in a 32-week randomized, double-blind, placebo-controlled study (4). One received omalizumab and the other a placebo. The twin receiving omalizumab was able to reduce her long-term treatment with fluticasone to 500 μg/day, while the other required treatment with fluticasone at a dose of 1250 μg/day and regular courses of oral corticosteroids due to persistent exacerbations. They were both then treated with omalizumab during a 6-year extension phase. During this time, there was clinical improvement with the absence of hospitalizations for severe attacks, disappearance of pollen-induced rhinitis and improved respiratory function (Fig. 1) under reduced long-term treatment with fluticasone 500 μg/day and occasional administration of oral corticosteroids. The adult height of the twin who first received omalizumab was 159 cm compared with 156 cm for the other. Change in respiratory function: observation of monozygotic twin sisters treated for 6 years with omalizumab. Twin 1, treated with omalizumab from the start. Twin 2, treated with the placebo and then omalizumab. The effectiveness of omalizumab in adolescents has previously been demonstrated in a pooled analysis showing that the relative risk of an adolescent aged between 12 and <18 presenting an asthma exacerbation when treated with omalizumab was 0.470 compared with the control group (95% CI: 0.318–0.695; P = 0.0002) (5). Our observation of monozygotic twins one treated with omalizumab and the other with a placebo for 32 weeks, then both with omalizumab for 6 years, and living in the same environment, supports these findings and suggests the effectiveness of omalizumab on a specific phenotype of severe asthma. Moreover, treatment with omalizumab produced progressive improvement in respiratory function in these twins which was not significantly demonstrated in the core study. The improvement in respiratory function in these complex cases of obstructive bronchopathy, in part linked to a history of severe neonatal respiratory disease, could be explained by: (i) a strong allergic phenotype associated with severe allergic asthma, pollen-induced rhinitis and atopic dermatitis and (ii) the particularly prolonged duration of treatment with omalizumab. The second distinctive feature of these observations was the possibility of reducing doses of inhaled corticosteroids earlier, particularly in the twin who received omalizumab from the start, at puberty, a crucial age for growth. It has been recognized, moreover, that the high-dose corticosteroid therapy required to control severe asthma can cause growth retardation (6). These observations suggest the beneficial effects of treatment with omalizumab in severe allergic asthma (i) on respiratory function when there is a strong allergic phenotype and treatment is continued over a long period and (ii) on maintaining the height/weight growth curve compared with prolonged treatment with high doses of inhaled corticosteroids, particularly during puberty.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
nico完成签到,获得积分10
1秒前
可爱的函函应助Tsin778采纳,获得10
1秒前
科研通AI2S应助曹志伟采纳,获得10
1秒前
1秒前
赘婿应助Thinkol采纳,获得10
1秒前
2秒前
YuexYue完成签到,获得积分10
3秒前
英姑应助cckk采纳,获得10
3秒前
hkh发布了新的文献求助10
3秒前
3秒前
3秒前
VISIN发布了新的文献求助10
3秒前
doudou发布了新的文献求助10
3秒前
喜羊羊发布了新的文献求助10
4秒前
4秒前
4秒前
4秒前
LLL完成签到,获得积分10
5秒前
chr完成签到,获得积分10
5秒前
斯文败类应助sadd采纳,获得10
5秒前
赵慧完成签到,获得积分10
5秒前
量子星尘发布了新的文献求助10
5秒前
nico发布了新的文献求助10
5秒前
懒羊羊关注了科研通微信公众号
6秒前
牛马人发布了新的文献求助10
7秒前
7秒前
Sherlock完成签到,获得积分10
7秒前
酷波er应助徐爱琳采纳,获得10
7秒前
7秒前
小北发布了新的文献求助10
8秒前
嘉嘉完成签到,获得积分10
8秒前
PANXX完成签到,获得积分10
8秒前
量子星尘发布了新的文献求助10
8秒前
8秒前
羊羊发布了新的文献求助10
8秒前
大气月饼发布了新的文献求助10
9秒前
流星砸地鼠完成签到 ,获得积分10
10秒前
10秒前
茹茹发布了新的文献求助10
10秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Translanguaging in Action in English-Medium Classrooms: A Resource Book for Teachers 700
Exploring Nostalgia 500
Natural Product Extraction: Principles and Applications 500
Exosomes Pipeline Insight, 2025 500
Qualitative Data Analysis with NVivo By Jenine Beekhuyzen, Pat Bazeley · 2024 500
Advanced Memory Technology: Functional Materials and Devices 400
热门求助领域 (近24小时)
化学 材料科学 生物 医学 工程类 计算机科学 有机化学 物理 生物化学 纳米技术 复合材料 内科学 化学工程 人工智能 催化作用 遗传学 数学 基因 量子力学 物理化学
热门帖子
关注 科研通微信公众号,转发送积分 5667660
求助须知:如何正确求助?哪些是违规求助? 4887012
关于积分的说明 15121059
捐赠科研通 4826441
什么是DOI,文献DOI怎么找? 2584044
邀请新用户注册赠送积分活动 1538066
关于科研通互助平台的介绍 1496210