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经皮递送的耐受原性纳米颗粒诱导有效的免疫耐受以治疗哮喘。

Transdermally delivered tolerogenic nanoparticles induced effective immune tolerance for asthma treatment.

机构信息

Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry and Sichuan Province, Sichuan Engineering Laboratory for Plant-Sourced Drug and Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy, Sichuan University, Chengdu 610064, China.

School of Chemical Engineering, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK; Changzhou Institute of Advanced Manufacturing Technology, Changzhou 213164, China.

出版信息

J Control Release. 2024 Feb;366:637-649. doi: 10.1016/j.jconrel.2024.01.018. Epub 2024 Jan 17.

Abstract

Induction of antigen-specific immune tolerance for the treatment of allergic or autoimmune diseases is an attractive strategy. Herein, we investigated the protective effect of a transdermal microneedle patch against allergic asthma by stimulating allergen-specific immune tolerance. We fabricated biodegradable tolerogenic nanoparticles (tNPs) that are loaded with a model allergen ovalbumin (OVA) and an immunomodulator rapamycin, and filled the tNPs into microneedle tips by centrifugation to form sustained-release microneedles. After intradermal immunization, the microneedles successfully delivered the cargos into the skin and sustainedly released them for over 96 h. Importantly, the microneedles induced allergen-specific regulatory T cells (Treg), decreased the levels of pro-inflammatory cytokines and antibodies while increased anti-inflammation cytokines, finally leading to restored immune homeostasis. The lung tissue analysis illustrated that the sustained-release microneedles significantly reduced the infiltration of eosinophils, decreased the accumulation of mucus and collagen, and significantly relived asthma symptoms. Our results suggested that the sustained-release microneedle-based transdermal delivery system can induce antigen-specific immune tolerance with improved compliance and efficacy, providing a new therapeutic strategy for the treatment of allergic and autoimmune diseases.

摘要

诱导抗原特异性免疫耐受治疗过敏或自身免疫性疾病是一种很有吸引力的策略。在此,我们通过刺激过敏原特异性免疫耐受来研究透皮微针贴片对过敏性哮喘的保护作用。我们制备了载有模型过敏原卵清蛋白(OVA)和免疫调节剂雷帕霉素的可生物降解的免疫耐受纳米颗粒(tNPs),并通过离心将 tNPs 填充到微针尖端形成持续释放微针。经皮免疫后,微针成功地将载药递送到皮肤中,并持续释放超过 96 小时。重要的是,微针诱导了过敏原特异性调节性 T 细胞(Treg),降低了促炎细胞因子和抗体的水平,同时增加了抗炎细胞因子,最终恢复了免疫平衡。肺组织分析表明,持续释放微针显著减少了嗜酸性粒细胞的浸润,减少了粘液和胶原的积累,并显著缓解了哮喘症状。我们的结果表明,基于持续释放微针的透皮给药系统可以诱导抗原特异性免疫耐受,提高顺应性和疗效,为治疗过敏和自身免疫性疾病提供了一种新的治疗策略。

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