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TLR9 激动剂吸附于明矾佐剂可预防由热带无爪螨提取物引起的哮喘样反应。

TLR9 agonist adsorbed to alum adjuvant prevents asthma-like responses induced by Blomia tropicalis mite extract.

机构信息

Laboratory of Immunobiology, Department of Immunology, Institute of Biomedical Science, University of São Paulo (ICB/USP), São Paulo, Brazil.

Centro Nacional De Biopreparados, Department of Allergens, Havana, Cuba.

出版信息

J Leukoc Biol. 2019 Sep;106(3):653-664. doi: 10.1002/JLB.MA1218-475RR. Epub 2019 Jul 22.

Abstract

Blomia tropicalis mite is highly prevalent in tropical and subtropical regions and it is associated with allergic diseases such as rhinitis and asthma. By using an OVA-model of allergic lung disease, we have previously shown that sensitization in the presence of toll like receptors (TLRs) agonists attenuates subsequent OVA-induced allergic responses. Here, we evaluated the effect of CpG-ODN, a specific synthetic TLR-9 agonist, on the development of experimental asthma induced by Blomia tropicalis extract, a relevant source of aeroallergens. Among different protocols of Blomia tropicalis extract sensitization, the subcutaneous sensitization in the presence of alum adjuvant induced the highest Th2 responses, including high IgE levels. Adsorption of CpG to Blomia tropicalis extract/Alum attenuated the airway hyperreactivity, the infiltration of inflammatory cells including eosinophils, and the IL-5 content in BAL. In addition, lung peribronchial inflammatory infiltrate, mucus production and IL-5-producing CD3 CD4 T cells were significantly reduced in the Blomia tropicalis extract/Alum+CpG group. Importantly, CpG inhibited total IgE production as well as active systemic or cutaneous anaphylaxis reactions. Inhibition of pulmonary Th2 responses was associated with increased IL-10 production but not with IFN-γ production. Notably, in IL-10-deficient mice, sensitization with OVA/Alum+CpG resulted in intense lung neutrophilia and IFN-γ production, indicating that IL-10 is necessary to inhibit subsequent Th1 immunity. Our work highlights the mechanisms of allergy attenuation by CpG and it indicates the potential use of Alum-based formulation with CpG to treat allergic processes.

摘要

布氏嗜螨过敏原在热带和亚热带地区广泛存在,并与过敏疾病如鼻炎和哮喘相关。我们之前使用变应原性肺病的 OVA 模型表明,在 Toll 样受体(TLRs)激动剂存在下致敏可减轻随后的 OVA 诱导的过敏反应。在这里,我们评估了 CpG-ODN(一种特定的合成 TLR-9 激动剂)对布氏嗜螨过敏原引起的实验性哮喘发展的影响,布氏嗜螨过敏原是空气过敏原的一个相关来源。在不同的布氏嗜螨过敏原致敏方案中,存在明矾佐剂的皮下致敏诱导了最高的 Th2 反应,包括高 IgE 水平。CpG 吸附到布氏嗜螨过敏原/明矾中减弱了气道高反应性、炎症细胞包括嗜酸性粒细胞的浸润以及 BAL 中的 IL-5 含量。此外,布氏嗜螨过敏原/明矾+CpG 组肺周围支气管炎症浸润、黏液产生和产生 IL-5 的 CD3 CD4 T 细胞明显减少。重要的是,CpG 抑制了总 IgE 的产生以及全身或皮肤过敏反应的活性。肺部 Th2 反应的抑制与 IL-10 的产生增加有关,但与 IFN-γ 的产生无关。值得注意的是,在 IL-10 缺陷小鼠中,用 OVA/Alum+CpG 致敏导致肺部嗜中性粒细胞增多和 IFN-γ 产生,表明 IL-10 是抑制随后的 Th1 免疫所必需的。我们的工作强调了 CpG 减轻过敏的机制,并表明基于明矾的制剂与 CpG 联合使用治疗过敏过程的潜力。

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