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本文引用的文献

1
Trends of microneedle technology in the scientific literature, patents, clinical trials and internet activity.微针技术在科学文献、专利、临床试验和互联网活动中的趋势。
Biomaterials. 2021 Jan;267:120491. doi: 10.1016/j.biomaterials.2020.120491. Epub 2020 Nov 5.
2
Sustained unresponsiveness to peanut after long-term peanut epicutaneous immunotherapy.长期花生皮内免疫治疗后对花生持续无反应。
J Allergy Clin Immunol Pract. 2021 Jan;9(1):524-526. doi: 10.1016/j.jaip.2020.08.017. Epub 2020 Aug 22.
3
Food allergy immunotherapy: Oral immunotherapy and epicutaneous immunotherapy.食物过敏免疫疗法:口服免疫疗法和经皮免疫疗法。
Allergy. 2020 Jun;75(6):1337-1346. doi: 10.1111/all.14220. Epub 2020 Feb 28.
4
Biomarkers in Food Allergy Immunotherapy.食物过敏免疫治疗中的生物标志物。
Curr Allergy Asthma Rep. 2019 Dec 4;19(12):61. doi: 10.1007/s11882-019-0894-y.
5
Delivery of allergen powder for safe and effective epicutaneous immunotherapy.过敏原粉末给药用于安全有效的经皮免疫治疗。
J Allergy Clin Immunol. 2020 Feb;145(2):597-609. doi: 10.1016/j.jaci.2019.11.022. Epub 2019 Nov 27.
6
Microneedles coated with peanut allergen enable desensitization of peanut sensitized mice.微针涂层花生过敏原使花生致敏的小鼠脱敏。
J Control Release. 2019 Nov 28;314:38-47. doi: 10.1016/j.jconrel.2019.09.022. Epub 2019 Oct 15.
7
Intranasal nanoemulsion vaccine confers long-lasting immunomodulation and sustained unresponsiveness in a murine model of milk allergy.鼻腔内纳米乳剂疫苗可在牛奶过敏的小鼠模型中诱导持久的免疫调节和持续的无反应性。
Allergy. 2020 Apr;75(4):872-881. doi: 10.1111/all.14064. Epub 2019 Oct 11.
8
IL-13-induced intestinal secretory epithelial cell antigen passages are required for IgE-mediated food-induced anaphylaxis.IL-13 诱导的肠道分泌上皮细胞抗原传递对于 IgE 介导的食物诱导性过敏反应是必需的。
J Allergy Clin Immunol. 2019 Oct;144(4):1058-1073.e3. doi: 10.1016/j.jaci.2019.04.030. Epub 2019 Jun 5.
9
Microneedle Coating Methods: A Review with a Perspective.微针涂层方法:综述与展望。
J Pharmacol Exp Ther. 2019 Sep;370(3):555-569. doi: 10.1124/jpet.119.258707. Epub 2019 Jun 7.
10
The skin as an immune organ: Tolerance versus effector responses and applications to food allergy and hypersensitivity reactions.皮肤作为免疫器官:耐受与效应反应及其在食物过敏和超敏反应中的应用。
J Allergy Clin Immunol. 2019 Aug;144(2):362-374. doi: 10.1016/j.jaci.2019.03.021. Epub 2019 Apr 5.

在皮肤内进行靶向过敏原特异性免疫治疗可改善过敏原传递,从而诱导对花生脱敏。

Targeted allergen-specific immunotherapy within the skin improves allergen delivery to induce desensitization to peanut.

机构信息

Mary H. Weiser Food Allergy Center, University of Michigan, Ann Arbor, MI 48109, USA.

Department of Chemical Engineering, Texas Tech University, Lubbock, TX 79409, USA.

出版信息

Immunotherapy. 2022 May;14(7):539-552. doi: 10.2217/imt-2021-0206. Epub 2022 Feb 24.

DOI:10.2217/imt-2021-0206
PMID:35196877
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9043875/
Abstract

Epicutaneous immunotherapy (EPIT) with peanut has been demonstrated to be safe but efficacy may be limited by allergen uptake through the skin barrier. To enhance allergen uptake into the skin, the authors used peanut-coated microneedles and compared them with EPIT in a peanut allergy mouse model. Sensitized mice were treated with peanut-coated microneedles or peanut-EPIT and then challenged with peanut to determine protection. Treatment with peanut-coated microneedles was safe and showed enhanced desensitization to peanut compared with peanut-EPIT administered via a similar schedule. Protection was associated with reduced Th2 immune responses and mast cell accumulation in the intestine. Peanut-coated microneedles have the potential to present a safe method of improving allergen delivery for cutaneous immunotherapy.

摘要

经皮免疫疗法(EPIT)已被证实用于花生是安全的,但由于皮肤屏障对过敏原的摄取,疗效可能有限。为了增强过敏原进入皮肤,作者使用了涂有花生的微针,并在花生过敏小鼠模型中与 EPIT 进行了比较。致敏的小鼠用涂有花生的微针或花生-EPIT 治疗,然后用花生进行挑战以确定保护作用。涂有花生的微针治疗是安全的,与通过类似方案给予的花生-EPIT 相比,显示出增强的脱敏作用。保护作用与减少肠道中的 Th2 免疫反应和肥大细胞积累有关。涂有花生的微针有可能提供一种安全的方法,改善用于皮肤免疫疗法的过敏原传递。