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用于免疫球蛋白E介导的过敏预防性耐受的细胞疗法

Cell Therapy for Prophylactic Tolerance in Immunoglobulin E-mediated Allergy.

作者信息

Baranyi Ulrike, Farkas Andreas M, Hock Karin, Mahr Benedikt, Linhart Birgit, Gattringer Martina, Focke-Tejkl Margit, Petersen Arnd, Wrba Fritz, Rülicke Thomas, Valenta Rudolf, Wekerle Thomas

机构信息

Section of Transplantation Immunology, Department of Surgery, Medical University of Vienna, Vienna, Austria.

Division of Immunopathology, Department of Pathophysiology and Allergy Research, Center of Physiology and Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.

出版信息

EBioMedicine. 2016 May;7:230-9. doi: 10.1016/j.ebiom.2016.03.028. Epub 2016 Mar 20.

Abstract

BACKGROUND

Therapeutic strategies for the prophylaxis of IgE-mediated allergy remain an unmet medical need. Cell therapy is an emerging approach with high potential for preventing and treating immunological diseases. We aimed to develop a cell-based therapy inducing permanent allergen-specific immunological tolerance for preventing IgE-mediated allergy.

METHODS

Wild-type mice were treated with allergen-expressing bone marrow cells under a short course of tolerogenic immunosuppression (mTOR inhibition and costimulation blockade). Bone marrow was retrieved from a novel transgenic mouse ubiquitously expressing the major grass pollen allergen Phl p 5 as a membrane-anchored protein (BALB/c-Tg[Phlp5-GFP], here mPhl p 5). After transplantation recipients were IgE-sensitized at multiple time points with Phl p 5 and control allergen.

RESULTS

Mice treated with mPhl p 5 bone marrow did not develop Phl p 5-specific IgE (or other isotypes) despite repeated administration of the allergen, while mounting and maintaining a strong humoral response towards the control allergen. Notably, Phl p 5-specific T cell responses and allergic airway inflammation were also completely prevented. Interestingly allergen-specific B cell tolerance was maintained independent of Treg functions indicating deletional tolerance as underlying mechanism.

CONCLUSION

This proof-of-concept study demonstrates that allergen-specific immunological tolerance preventing occurrence of allergy can be established through a cell-based therapy employing allergen-expressing leukocytes.

摘要

背景

预防IgE介导的过敏的治疗策略仍未满足医学需求。细胞疗法是一种新兴的方法,在预防和治疗免疫性疾病方面具有很高的潜力。我们旨在开发一种基于细胞的疗法,诱导永久性的过敏原特异性免疫耐受,以预防IgE介导的过敏。

方法

在短期的致耐受性免疫抑制(mTOR抑制和共刺激阻断)下,用表达过敏原的骨髓细胞治疗野生型小鼠。骨髓取自一种新型转基因小鼠,该小鼠普遍表达主要草花粉过敏原Phl p 5作为膜锚定蛋白(BALB/c-Tg[Phlp5-GFP],此处为mPhl p 5)。移植后,受体在多个时间点用Phl p 5和对照过敏原进行IgE致敏。

结果

用mPhl p 5骨髓治疗的小鼠尽管反复给予过敏原,但未产生Phl p 5特异性IgE(或其他同种型),同时对对照过敏原产生并维持强烈的体液反应。值得注意的是,Phl p 5特异性T细胞反应和过敏性气道炎症也完全得到预防。有趣的是,过敏原特异性B细胞耐受的维持与调节性T细胞功能无关,表明缺失性耐受是潜在机制。

结论

这项概念验证研究表明,通过使用表达过敏原的白细胞的细胞疗法,可以建立预防过敏发生的过敏原特异性免疫耐受。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c770/4909362/07b40562b070/gr1.jpg

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