Cabauatan C R, Campana R, Niespodziana K, Reinisch C, Lundberg U, Meinke A, Henning R, Neubauer A, Valenta R
Division of Immunopathology, Department of Pathophysiology and Allergy Research, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.
Valneva Austria GmbH, Campus Vienna Biocenter, Vienna, Austria.
Allergy. 2017 Jan;72(1):164-168. doi: 10.1111/all.13036. Epub 2016 Sep 30.
Epicutaneous allergen-specific immunotherapy (EPIT) is proposed as an alternative route for allergen-specific immunotherapy (AIT). The induction of allergen-specific blocking IgG antibodies represents an important mechanism underlying AIT, but has not been investigated for EPIT. Here, we compared the induction of allergen-specific blocking IgG in outbred guinea pigs which had been immunized with recombinant birch pollen allergen Bet v 1 using patch delivery system (PDS) with or without heat-labile toxin (LT) from Escherichia coli or subcutaneously with aluminum hydroxide (Alum)-adsorbed rBet v 1. Only subcutaneous immunization with Alum-adsorbed rBet v 1 and epicutaneous administration of rBet v 1 with PDS in combination with LT from E. coli induced allergen-specific IgG antibodies blocking allergic patients' IgE, but not immunization with rBet v 1 via PDS alone. Our results suggest that patch vaccination with rBet v 1 in combination with LT may be a promising strategy for allergen-specific immunotherapy against birch pollen allergy.
表皮过敏原特异性免疫疗法(EPIT)被提议作为过敏原特异性免疫疗法(AIT)的一种替代途径。过敏原特异性阻断IgG抗体的诱导是AIT的一个重要潜在机制,但尚未针对EPIT进行研究。在此,我们比较了用重组桦树花粉过敏原Bet v 1通过贴片给药系统(PDS)免疫的远交豚鼠中,过敏原特异性阻断IgG的诱导情况,其中PDS有或没有来自大肠杆菌的不耐热毒素(LT),或者皮下注射用氢氧化铝(Alum)吸附的rBet v 1。只有皮下注射用Alum吸附的rBet v 1以及用PDS联合来自大肠杆菌的LT经皮给予rBet v 1能诱导出阻断过敏患者IgE的过敏原特异性IgG抗体,而单独通过PDS用rBet v 1免疫则不能。我们的结果表明,用rBet v 1联合LT进行贴片疫苗接种可能是针对桦树花粉过敏的过敏原特异性免疫疗法的一种有前景的策略。