黑胸蝮蛇毒液过敏:特异性免疫治疗选择的抑制研究方法。

V Grossi, M Severino, A Massolo, M Infantino, F Laureti, D Macchia, E Meucci, E Francescato, B Pantera, A Ebbli, F Fumagalli, B Lari, A Perri, I Liotti, G Ciotta, G Terenzi, S V Valeva, M Consolati, T Folgore, M Manfredi
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引用次数: 1

摘要

摘要:黑斑黄蜂(Vespa velutina nigrithorax, VVN),因在亚洲特有而被称为亚洲黄蜂,是欧洲的外来种。据报道,VVN可引起与其他膜翅目昆虫类似的过敏反应,并在VVN蜇伤后死亡,可能是由于致命的过敏反应。在膜翅目毒液过敏的治疗中,特异性免疫疗法(VIT)是非常有效的。目前,没有针对VVN的特异性VIT,因此评估被VVN蜇伤并出现过敏反应的患者是否可以用市售的膜翅目Vespa crabro (VC)和Vespula spp (Vspp)提取物治疗,或者是否需要使用VVN毒液提取物进行特异性VIT是相关的。方法。对4例静脉毒刺后出现全身反应的患者进行临床评价。采用Phadia™1000系统(Thermo Fisher Scientific, Uppsala, Sweden)的自动荧光酶免疫分析法对血清特异性IgE进行定量检测,检测VC、Vspp和VVN。在每种毒液浓度为200 μl的血清样品中进行Cap抑制实验,随后使用Phadia™250系统(Thermo Fisher Scientific, Uppsala, Sweden)检测样品中针对每种毒液的特异性IgE。结果。我们的研究结果表明,Vspp和VC毒液都能抑制VVN的特异性IgE,尽管VC毒液比Vspp毒液表现出更高的抑制作用。结论。我们的抑制研究表明,在目前没有针对VVN的特异性VIT的情况下,VC毒液的VIT可能比Vspp VIT对VVN刺痛反应的患者更有效。
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Vespa velutina nigrithorax venom allergy: inhibition studies approach for the choice of specific immunotherapy.

Summary: Vespa velutina nigrithorax (VVN), commonly known as Asian wasp because endemic in Asia, represents an alien species in Europe. VVN can induce allergic reactions similar to those caused by other Hymenoptera and death after VVN stings, presumably due to fatal allergic reactions, has been reported. In the treatment of Hymenoptera venom hypersensitivity, specific immunotherapy (VIT) is highly effective. Currently, there is no specific available VIT for VVN, so it is relevant to assess if patients stung by VVN and showing allergic reactions could be treated with the Hymenoptera commercially available extracts Vespa crabro (VC) and Vespula spp (Vspp) or if they need the specific VIT with VVN venom extract. Methods. Four patients with a clinical history of systemic reactions after VVN sting were evaluated. Serum specific IgE were assayed quantitatively with an automated fluoro-enzyme immunoassay ImmunoCAP™ Specific IgE by Phadia™ 1000 System (Thermo Fisher Scientific, Uppsala, Sweden) for VC, Vspp and VVN. Cap inhibition assays were performed incubating serum samples with 200 μl of each venom at increasing concentrations and subsequently specific IgE against each of the venoms were determined in the samples by Phadia™ 250 System (Thermo Fisher Scientific, Uppsala, Sweden). Results. Our results suggested that both Vspp and VC venoms were able to inhibit the specific IgE for VVN, although the VC compared to the Vspp venom showed a higher inhibition. Conclusions. Our inhibition studies suggested that VIT with VC venom, nowadays when there is not specific available VIT for VVN, may be more effective than Vspp VIT in patients with VVN sting reactions.

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