Szépfalusi Z, Loibichler C, Hänel-Dekan S, Dehlink E, Gerstmayr M, Pichler J, Eiwegger T, Horvat R, Urbanek R
Department of Pediatrics and Juvenile Medicine, Medical University of Vienna, Vienna, Austria.
Clin Exp Allergy. 2006 Sep;36(9):1130-7. doi: 10.1111/j.1365-2222.2006.02559.x.
Transplacental transfer of nutritive and inhalant allergens has been described being potentially responsible for a series of events leading to antigen-specific immune responses in the fetus. As such, cord blood T cell responses appear ubiquitously. However, studies failed to reveal a consistent dose-response relationship between antenatal allergen exposure and allergen-specific cellular reactivity in cord blood.
To examine the transfer process of allergens (ovalbumin (OVA), beta-lactoglobulin (BLG), birch pollen allergen Bet v1) in placental tissue (BeWo cell line, ex vivo placenta model).
The choriocarcinoma cell line BeWo was used to study the allergen uptake and transfer experiments in vitro. In the ex vivo placenta model the contribution of different placental compartments was evaluated. For this, immuno-histochemistry, immuno-electronmicroscopy and ELISA techniques were applied using monoclonal antibodies to Bet v1, OVA and -BLG.
In vitro transfer studies on a BeWo cell-layer revealed an intracellular allergen uptake and a trans-trophoblastic allergen transfer, which was temperature- and concentration dependent, pH sensitive and asymmetric. Allergen-specific staining of placental tissue after allergen perfusion (BLG) demonstrated bulk of the allergen in the syncytio-trophoblastic cell layer and minor staining in the villous stroma and in the endothelium of fetal vessels. Immunogold staining revealed an accumulation of the perfused allergen in the trophoblastic basement membrane.
In vitro/ex vivo trans-trophoblastic and trans-placental allergen transfer is shown with an accumulation of most of the allergen in placental tissues, potentially explaining the missing direct dose-response relationship between prenatal (maternal) allergen exposure and allergen-specific cellular reactivity in cord blood.
营养性和吸入性过敏原的经胎盘转移被认为可能是导致胎儿发生抗原特异性免疫反应的一系列事件的原因。因此,脐血T细胞反应普遍存在。然而,研究未能揭示产前过敏原暴露与脐血中过敏原特异性细胞反应性之间一致的剂量反应关系。
研究过敏原(卵清蛋白(OVA)、β-乳球蛋白(BLG)、桦树花粉过敏原Bet v1)在胎盘组织(BeWo细胞系、离体胎盘模型)中的转移过程。
采用绒毛膜癌细胞系BeWo进行体外过敏原摄取和转移实验。在离体胎盘模型中,评估了不同胎盘隔室的作用。为此,使用针对Bet v1、OVA和-BLG的单克隆抗体,应用免疫组织化学、免疫电子显微镜和ELISA技术。
对BeWo细胞层进行的体外转移研究显示,存在细胞内过敏原摄取和跨滋养层过敏原转移,其具有温度和浓度依赖性、pH敏感性且不对称。过敏原灌注后(BLG)胎盘组织的过敏原特异性染色显示,大部分过敏原位于合体滋养层细胞层,绒毛基质和胎儿血管内皮细胞中的染色较少。免疫金染色显示灌注的过敏原在滋养层基底膜中积累。
体外/离体跨滋养层和经胎盘过敏原转移得以证实,大部分过敏原在胎盘组织中积累,这可能解释了产前(母体)过敏原暴露与脐血中过敏原特异性细胞反应性之间缺乏直接剂量反应关系的原因。