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[特异性免疫疗法:重组分子主要变应原和低变应原性变体的临床经验]

[Specific immunotherapy : clinical experience with recombinant molecular major allergens and hypoallergenic variants].

作者信息

Schendzielorz P, Klimek L

机构信息

HNO-Universitätsklinik Würzburg, Würzburg, Deutschland.

出版信息

HNO. 2013 Oct;61(10):834-42. doi: 10.1007/s00106-013-2730-3.

DOI:10.1007/s00106-013-2730-3
PMID:23913191
Abstract

Currently, preparations containing native allergens or allergoids are used predominantly in allergen-specific immunotherapy (SIT) of inhaled allergies. The safety and efficacy of these preparations has been demonstrated. However, their reproducible production and standardisation requires substantial effort. Besides this, improved efficacy is often associated with higher doses and an increase in adverse events. The production of recombinant allergens could make SIT preparations more precisely definable, purer, more reproducible, safer and more efficacious. Furthermore, a more specific and individually tailored therapy would be conceivable. These effects could be further amplified by modification to hypoallergenic variants and peptides, or by the addition of adjuvants. Results of clinical trials with recombinant grass, birch and ragweed pollen, as well as with cat hair allergens have already been published. Particularly broad clinical experience exists for recombinant birch and grass pollen preparations, and results are promising for commercial application. Taken as a whole, this new technology can both improve the therapy of allergic diseases and deepen the understanding of the molecular mechanisms of SIT.

摘要

目前,含有天然变应原或类变应原的制剂主要用于吸入性过敏的变应原特异性免疫疗法(SIT)。这些制剂的安全性和有效性已得到证实。然而,其可重复生产和标准化需要付出巨大努力。除此之外,疗效的提高往往伴随着更高的剂量和不良事件的增加。重组变应原的生产可以使SIT制剂更精确、更纯净、更可重复、更安全且更有效。此外,还可以设想一种更具特异性和个性化定制的疗法。通过修饰为低变应原性变体和肽,或添加佐剂,这些效果可能会进一步增强。重组草、桦树和豚草花粉以及猫毛变应原的临床试验结果已经发表。重组桦树和草花粉制剂拥有特别广泛的临床经验,其结果有望用于商业应用。总体而言,这项新技术既能改善过敏性疾病的治疗,又能加深对SIT分子机制的理解。

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本文引用的文献

1
Specific subcutaneous immunotherapy with recombinant grass pollen allergens: first randomized dose-ranging safety study.特定的重组草花粉过敏原皮下免疫治疗:首个随机剂量范围安全性研究。
Clin Exp Allergy. 2012 Jun;42(6):936-45. doi: 10.1111/j.1365-2222.2012.03971.x.
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Intralymphatic immunotherapy for cat allergy induces tolerance after only 3 injections.猫过敏的淋巴内免疫治疗仅需 3 次注射即可诱导耐受。
J Allergy Clin Immunol. 2012 May;129(5):1290-6. doi: 10.1016/j.jaci.2012.02.026. Epub 2012 Mar 30.
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Assessment of clinical efficacy of CYT003-QbG10 in patients with allergic rhinoconjunctivitis: a phase IIb study.
评估 CYT003-QbG10 治疗过敏性鼻结膜炎患者的临床疗效:一项 IIb 期研究。
Clin Exp Allergy. 2011 Sep;41(9):1305-12. doi: 10.1111/j.1365-2222.2011.03783.x. Epub 2011 Jun 14.
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Immunotherapy with peptides.肽免疫疗法。
Allergy. 2011 Jun;66(6):784-91. doi: 10.1111/j.1398-9995.2011.02610.x. Epub 2011 Apr 20.
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Recombinant allergens for specific immunotherapy.用于特异性免疫治疗的重组变应原。
J Allergy Clin Immunol. 2011 Apr;127(4):865-72. doi: 10.1016/j.jaci.2011.01.047. Epub 2011 Mar 5.
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Recombinant allergens for allergen-specific immunotherapy: 10 years anniversary of immunotherapy with recombinant allergens.重组变应原在变应原特异性免疫治疗中的应用:重组变应原免疫治疗 10 周年。
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J Allergy Clin Immunol. 2011 Jan;127(1):89-97, 97.e1-14. doi: 10.1016/j.jaci.2010.11.029.
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Allergic rhinitis: Direct and indirect costs.变应性鼻炎:直接和间接费用。
Allergy Asthma Proc. 2010 Sep-Oct;31(5):375-80. doi: 10.2500/aap.2010.31.3329.
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Antigen specificity is not required for modulation of lung allergic responses by naturally occurring regulatory T cells.天然存在的调节性T细胞对肺部过敏反应的调节并不需要抗原特异性。
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Intralymphatic allergen administration renders specific immunotherapy faster and safer: a randomized controlled trial.淋巴管内给予变应原使特异性免疫治疗更快且更安全:一项随机对照试验。
Proc Natl Acad Sci U S A. 2008 Nov 18;105(46):17908-12. doi: 10.1073/pnas.0803725105. Epub 2008 Nov 10.