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通过黏膜应用源自-的分子减少过敏性肺病:碳水化合物的可能作用

Reduction of Allergic Lung Disease by Mucosal Application of -Derived Molecules: Possible Role of Carbohydrates.

作者信息

Korb Elke, Drinić Mirjana, Wagner Angelika, Geissler Nora, Inic-Kanada Aleksandra, Peschke Roman, Joachim Anja, Wiedermann Ursula, Schabussova Irma

机构信息

Institute of Specific Prophylaxis and Tropical Medicine, Medical University of Vienna, Vienna, Austria.

Department of Pathobiology, Institute of Parasitology, University of Veterinary Medicine Vienna, Vienna, Austria.

出版信息

Front Immunol. 2021 Mar 10;11:612766. doi: 10.3389/fimmu.2020.612766. eCollection 2020.


DOI:10.3389/fimmu.2020.612766
PMID:33776987
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7988086/
Abstract

BACKGROUND: The hygiene hypothesis suggests a link between parasitic infections and immune disorders, such as allergic diseases. We previously showed that infection with or systemic application of tachyzoites lysate antigen (TLA) in a prophylactic, but not therapeutic protocol, prevented allergic airway inflammation in mice. Here we tested the effect of prophylactic and therapeutic application of TLA the mucosal route. METHODS: Mice were intranasally treated with TLA either i) prior to sensitization, ii) during sensitization and challenge, or iii) after sensitization with ovalbumin (OVA). Recruitment of inflammatory cells to the lung, cytokine levels in restimulated lung and spleen cell cultures as well as levels of OVA-specific antibodies in serum were measured. In parallel, the effect of native TLA, heat-inactivated (hiTLA) or deglycosylated TLA (dgTLA) on sensitized splenocytes was evaluated . RESULTS: When applied together with OVA i) during systemic sensitization and local challenge or ii) exclusively during local challenge, TLA reduced infiltration of eosinophils into the lung, OVA-specific type 2 cytokines in restimulated lung cell cultures, and partially, type 2 cytokines in restimulated spleen cell cultures in comparison to allergic controls. No beneficial effect was observed when TLA was applied prior to the start of sensitization. Analysis of epitope sugars on TLA indicated a high abundance of mannose, fucose, N-acetylglucosamine, and N-acetylgalactosamine. Deglycosylation of TLA, but not heat-inactivation, abolished the potential of TLA to reduce type 2 responses , suggesting a significant role of carbohydrates in immunomodulation. CONCLUSION: We showed that mucosal application of TLA reduced the development of experimental allergy in mice. The beneficial effects depended on the timing of the application in relation to the time point of sensitization. Not only co-application, but also therapy in sensitized/allergic animals with native TLA reduced local allergic responses. Furthermore, we show that TLA is highly glycosylated and glycoconjugates seem to play a role in anti-allergic effects. In summary, given the powerful modulatory effect that TLA exhibits, understanding its exact mechanisms of action may lead to the development of novel immunomodulators in clinical application.

摘要

背景:卫生假说表明寄生虫感染与免疫紊乱之间存在联系,如过敏性疾病。我们之前表明,在预防性而非治疗性方案中,用速殖子裂解物抗原(TLA)感染或全身应用TLA可预防小鼠过敏性气道炎症。在此,我们测试了经黏膜途径预防性和治疗性应用TLA的效果。 方法:用TLA对小鼠进行鼻内治疗,具体如下:i)在致敏前;ii)在致敏和激发期间;iii)在用卵清蛋白(OVA)致敏后。测量炎症细胞向肺的募集、再刺激的肺和脾细胞培养物中的细胞因子水平以及血清中OVA特异性抗体的水平。同时,评估天然TLA、热灭活TLA(hiTLA)或去糖基化TLA(dgTLA)对致敏脾细胞的影响。 结果:与过敏性对照组相比,当TLA与OVA一起应用时:i)在全身致敏和局部激发期间,或ii)仅在局部激发期间,TLA可减少嗜酸性粒细胞向肺的浸润、再刺激的肺细胞培养物中OVA特异性2型细胞因子的产生,以及部分减少再刺激的脾细胞培养物中2型细胞因子的产生。在致敏开始前应用TLA未观察到有益效果。对TLA上表位糖的分析表明,甘露糖、岩藻糖、N - 乙酰葡糖胺和N - 乙酰半乳糖胺含量很高。TLA去糖基化而非热灭活消除了TLA降低2型反应的潜力,表明碳水化合物在免疫调节中起重要作用。 结论:我们表明经黏膜应用TLA可减少小鼠实验性过敏的发生。有益效果取决于应用时间与致敏时间点的关系。不仅联合应用,而且用天然TLA对致敏/过敏动物进行治疗也可减少局部过敏反应。此外,我们表明TLA高度糖基化,糖缀合物似乎在抗过敏作用中起作用。总之,鉴于TLA表现出强大的调节作用,了解其确切作用机制可能会导致临床应用中新型免疫调节剂的开发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/615a/7988086/c730a81ed4ff/fimmu-11-612766-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/615a/7988086/0184da711a47/fimmu-11-612766-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/615a/7988086/470424748fab/fimmu-11-612766-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/615a/7988086/ce34668e85c7/fimmu-11-612766-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/615a/7988086/a083b1725f13/fimmu-11-612766-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/615a/7988086/82ad5f5ffdce/fimmu-11-612766-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/615a/7988086/13fe3609238e/fimmu-11-612766-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/615a/7988086/c730a81ed4ff/fimmu-11-612766-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/615a/7988086/0184da711a47/fimmu-11-612766-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/615a/7988086/470424748fab/fimmu-11-612766-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/615a/7988086/ce34668e85c7/fimmu-11-612766-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/615a/7988086/a083b1725f13/fimmu-11-612766-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/615a/7988086/82ad5f5ffdce/fimmu-11-612766-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/615a/7988086/13fe3609238e/fimmu-11-612766-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/615a/7988086/c730a81ed4ff/fimmu-11-612766-g007.jpg

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[3]
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[4]
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[5]
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[6]
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[10]
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