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儿童使用狗和猫提取物进行免疫治疗。

Immunotherapy with dog and cat extracts in children.

作者信息

Bertelsen A, Andersen J B, Christensen J, Ingemann L, Kristensen T, Ostergaard P A

机构信息

Department of Paediatrics, Frederiksborg County Hospital, Hillerød, Denmark.

出版信息

Allergy. 1989 Jul;44(5):330-5. doi: 10.1111/j.1398-9995.1989.tb00454.x.

Abstract

Hypersensitivity to dogs and cats causes asthma in many children. In this open controlled clinical study we wanted to establish whether immunotherapy can be recommended as a supplement to conventional medical therapy in dog- and cat-induced asthma in children. Twenty-seven children with mean age 10 7/12 years and with allergy to dog or cat according to anamnesis, skin prick test (SPT), specific IgE (RAST) and bronchial provocation test (BPT) entered the study. On the basis of age and bronchial sensitivity they were randomly allocated to either immunotherapy with dog or cat extract (active group, n = 14) or conventional medical therapy (control group, n = 13). Immunotherapy comprised subcutaneous injections with an alum-adsorbed depot extract (Alutard-SQ), and a maintenance dose of 100,000 SQ-U or the maximum tolerated dose. Before entering the study and after 9 months' therapy the patients were evaluated by BPT, SPT, RAST - and IgG4 analyses. The active group showed statistically significant change in bronchial tolerance (P less than 0.02), whereas no such change was found in the control group (P greater than 0.05). The change in skin sensitivity was significantly greater in the active group than in the control group (P less than 0.05), whereas no significant differences were found in RAST and IgG4. However, a significant (P = 0.05) increase in IgG4 was seen in the active but not in the control group. Frequency and degree of side effects in this study were acceptable.

摘要

对狗和猫过敏会导致许多儿童患哮喘。在这项开放性对照临床研究中,我们想确定免疫疗法是否可作为儿童狗和猫诱发哮喘的传统药物治疗的补充方法。27名平均年龄为10又7/12岁、根据既往病史、皮肤点刺试验(SPT)、特异性IgE(RAST)和支气管激发试验(BPT)对狗或猫过敏的儿童进入了该研究。根据年龄和支气管敏感性,他们被随机分为用狗或猫提取物进行免疫疗法(治疗组,n = 14)或传统药物治疗(对照组,n = 13)。免疫疗法包括皮下注射明矾吸附的长效提取物(Alutard-SQ),维持剂量为100,000 SQ-U或最大耐受剂量。在进入研究前和治疗9个月后,通过BPT、SPT、RAST和IgG4分析对患者进行评估。治疗组的支气管耐受性有统计学意义的变化(P < 0.02),而对照组未发现此类变化(P > 0.05)。治疗组皮肤敏感性的变化明显大于对照组(P < 0.05),而RAST和IgG4未发现显著差异。然而,治疗组的IgG4有显著(P = 0.05)升高,而对照组没有。本研究中副作用的频率和程度是可接受的。

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