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蠕虫、过敏性疾病与IgE介导的免疫反应:我们目前的研究进展如何?

Helminths, allergic disorders and IgE-mediated immune responses: where do we stand?

作者信息

Erb Klaus J

机构信息

Department of Pulmonary Research, Boehringer Ingelheim Pharma GmbH & Co. KG, Biberach Riss, Germany.

出版信息

Eur J Immunol. 2007 May;37(5):1170-3. doi: 10.1002/eji.200737314.

DOI:10.1002/eji.200737314
PMID:17447233
Abstract

Th2 responses induced by allergens or helminths share many common features. However, allergen-specific IgE can almost always be detected in atopic patients, whereas helminth-specific IgE is often not detectable and anaphylaxis often occurs in atopy but not helminth infections. This may be due to T regulatory responses induced by the helminths or the lack of helminth-specific IgE. Alternatively non-specific IgE induced by the helminths may protect from mast cell or basophil degranulation by saturating IgE binding sites. Both of these mechanisms have been implicated to be involved in helminth-induced protection from allergic responses. An article in the current issue of the European Journal of Immunology describes the generation of an anti-Nippostrongylus brasiliensis-specific IgE antibody which was used to identify a novel N. brasiliensis antigen (Nb-Ag1). The authors demonstrated that Nb-Ag1 specific IgE could only be detected for a short period of time during infection, and that these levels were sufficient to prime mast cells thereby leading to active cutaneous anaphylaxis after the application of Nb-Ag1. This is the first report clearly showing that a low level of helminth-specific IgE, transiently produced, is able to induce mast cell degranulation in the presence of large amounts of polyclonal IgE.

摘要

由过敏原或蠕虫诱导的Th2反应具有许多共同特征。然而,在特应性患者中几乎总能检测到过敏原特异性IgE,而蠕虫特异性IgE往往检测不到,并且过敏反应常发生在特应性患者中而非蠕虫感染时。这可能是由于蠕虫诱导的T调节反应或缺乏蠕虫特异性IgE。或者,蠕虫诱导的非特异性IgE可能通过饱和IgE结合位点来保护机体免受肥大细胞或嗜碱性粒细胞脱颗粒的影响。这两种机制都被认为与蠕虫诱导的对过敏反应的保护作用有关。本期《欧洲免疫学杂志》上的一篇文章描述了一种抗巴西日圆线虫特异性IgE抗体的产生,该抗体被用于鉴定一种新的巴西日圆线虫抗原(Nb-Ag1)。作者证明,在感染期间只能在短时间内检测到Nb-Ag1特异性IgE,并且这些水平足以使肥大细胞致敏,从而在应用Nb-Ag1后导致主动皮肤过敏反应。这是第一份明确表明短暂产生的低水平蠕虫特异性IgE能够在存在大量多克隆IgE的情况下诱导肥大细胞脱颗粒的报告。

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