Jeong Kyoung Yong, Hongb Chein-Soo, Yong Tai-Soon
Department of Parasitology and Institute of Tropical Medicine, Brain Korea 21 Project for Medical Science, Yonsei University College of Medicine, Seoul, Korea.
Curr Protein Pept Sci. 2006 Feb;7(1):57-71. doi: 10.2174/138920306775474112.
The prevalence of allergic disorders has increased over the past few decades and the quality of life has been significantly influenced at least for the allergic subjects. Allergen avoidance is thought to be the best way of preventing clinical manifestation of the disease, however, it is not possible for some allergens, and other pharmacological and/or immunological treatment has to be made. Repetitive injection of sensitized allergens to the patients (immunotherapy) is the only known curative approach to the disease even though the exact mechanism is not clear to date. Crude extract of allergens has lots of shortcomings which might arouse unexpected results. Genetic engineering and recombinant allergens are thought to be one of the alternative ways to overcome these limitations. Genetic engineering could facilitate the investigation of immune responses of the subjects especially on B cell and T cell epitopes, and produce the therapeutic allergens which might minimize the possible side effects. Furthermore, conjugation of immuno-modulatory molecules such as CpG-ODN, cytokines, or toxins which could act specifically to the given allergens, and maleylation of the allergens could maximize the prophylactic or therapeutic effect. Immunotherapies for the pollen allergy and insect sting allergy have been thought to be successful. House dust mite allergy and cockroach allergy have been reported less beneficial by immunotherapeutic approaches. Cockroaches are one of the most important causes of asthma, and severe complications are often reported in the children in city dwellers with low-incomes. The studies of the biological functions of cockroach allergens and the use of recombinant allergens should allow understanding of mechanisms of cockroach-elicited allergic disorders and development of allergen-specific and sensitive diagnostics and tailored therapeutic approaches in the future.
在过去几十年中,过敏性疾病的患病率有所上升,至少对过敏患者而言,生活质量受到了显著影响。避免接触过敏原被认为是预防该疾病临床表现的最佳方法,然而,对于某些过敏原来说这是不可能的,因此必须采取其他药物和/或免疫治疗方法。向患者重复注射致敏过敏原(免疫疗法)是目前已知的治疗该疾病的唯一方法,尽管确切机制至今尚不清楚。过敏原粗提物存在许多缺点,可能会引发意想不到的结果。基因工程和重组过敏原被认为是克服这些局限性的替代方法之一。基因工程有助于研究受试者的免疫反应,特别是对B细胞和T细胞表位的免疫反应,并生产出可能将副作用降至最低的治疗性过敏原。此外,将能特异性作用于特定过敏原的免疫调节分子(如CpG-ODN、细胞因子或毒素)进行偶联,以及对过敏原进行马来酰化处理,可以使预防或治疗效果最大化。花粉过敏和昆虫叮咬过敏的免疫疗法被认为是成功的。据报道,屋尘螨过敏和蟑螂过敏的免疫治疗效果较差。蟑螂是哮喘的最重要病因之一,在低收入城市居民的儿童中,经常有严重并发症的报道。对蟑螂过敏原生物学功能的研究以及重组过敏原的应用,有望在未来帮助我们理解蟑螂引发的过敏性疾病的机制,并开发出过敏原特异性、灵敏的诊断方法以及量身定制的治疗方法。