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过敏诊断与治疗的分子方法。

Molecular approach to allergy diagnosis and therapy.

作者信息

Ferreira Fatima, Wolf Martin, Wallner Michael

机构信息

Christian Doppler Laboratory for Allergy Diagnosis and Therapy, Department of Molecular Biology, University of Salzburg, Salzburg, Austria.

出版信息

Yonsei Med J. 2014 Jul;55(4):839-52. doi: 10.3349/ymj.2014.55.4.839.

Abstract

Presently, allergy diagnosis and therapy procedures are undergoing a transition phase in which allergen extracts are being step-by-step replaced by molecule-based products. The new developments will allow clinicians to obtain detailed information on sensitization patterns, more accurate interpretation of allergic symptoms, and thus improved patients' management. In this respect, recombinant technology has been applied to develop this new generation of molecule-based allergy products. The use of recombinant allergens allows full validation of identity, quantity, homogeneity, structure, aggregation, solubility, stability, IgE-binding and the biologic potency of the products. In contrast, such parameters are extremely difficult to assay and standardize for extract-based products. In addition to the possibility of bulk production of wild type molecules for diagnostic purposes, recombinant technology opened the possibility of developing safer and more efficacious products for allergy therapy. A number of molecule-based hypoallergenic preparations have already been successfully evaluated in clinical trials, bringing forward the next generation of allergy vaccines. In this contribution, we review the latest developments in allergen characterization, molecule-based allergy diagnosis, and the application of recombinant allergens in therapeutic setups. A comprehensive overview of clinical trials using recombinant allergens as well as synthetic peptides is presented.

摘要

目前,过敏诊断和治疗程序正处于转型阶段,在此阶段,变应原提取物正逐步被基于分子的产品所取代。这些新进展将使临床医生能够获得关于致敏模式的详细信息,更准确地解释过敏症状,从而改善对患者的管理。在这方面,重组技术已被应用于开发新一代基于分子的过敏产品。重组变应原的使用使得产品的身份、数量、均一性、结构、聚集、溶解性、稳定性、IgE结合及生物活性能够得到充分验证。相比之下,基于提取物的产品极难对这些参数进行测定和标准化。除了有可能大量生产用于诊断目的的野生型分子外,重组技术还为开发更安全、更有效的过敏治疗产品开辟了可能性。一些基于分子的低变应原性制剂已在临床试验中成功得到评估,从而催生了新一代过敏疫苗。在本论文中,我们综述了变应原表征、基于分子的过敏诊断以及重组变应原在治疗中的应用方面的最新进展。本文还全面概述了使用重组变应原以及合成肽的临床试验情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/334e/4075386/efb2bfd8c810/ymj-55-839-g001.jpg

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