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含过敏原的HVJ-E无针鼻内给药可减轻实验性变应性鼻炎。

Needleless intranasal administration of HVJ-E containing allergen attenuates experimental allergic rhinitis.

作者信息

Yasuoka Eri, Oshima Kazuo, Tamai Katsuto, Kubo Takeshi, Kaneda Yasufumi

机构信息

Department of Gene Therapy Science, Graduate School of Medicine, Osaka University, 2-2 Yamadaoka, Suita, Osaka 565-0871, Japan.

出版信息

J Mol Med (Berl). 2007 Mar;85(3):283-92. doi: 10.1007/s00109-006-0120-y. Epub 2006 Oct 28.

Abstract

Allergic rhinitis (AR) is one of the most common chronic diseases. Although current medications are highly effective in controlling its symptoms, they do not reverse the allergen-specific hypersensitivities that underlie the disease. Immunoglobulin E is a key mediator of AR, and preventing its production is clinically important. In this study, we developed an efficient needleless intranasal protein delivery system using the hemagglutinating virus of Japan envelope vector (HVJ-E). Intranasal delivery of ovalbumin (OVA) once a week for 3 weeks using this system enhanced OVA-induced interferon-gamma production by murine splenocytes. This treatment also attenuated the OVA-induced release interleukin-4 (IL-4) and IL-5 from splenocytes and the production of plasma OVA-specific immunoglobulin E in OVA-sensitive AR model mice. Thus, allergen-containing HVJ-E may be useful for noninvasive treatment of AR.

摘要

变应性鼻炎(AR)是最常见的慢性疾病之一。尽管目前的药物在控制其症状方面非常有效,但它们并不能逆转作为该疾病基础的变应原特异性超敏反应。免疫球蛋白E是AR的关键介质,阻止其产生在临床上具有重要意义。在本研究中,我们利用日本血凝病毒包膜载体(HVJ-E)开发了一种高效的无针鼻内蛋白递送系统。使用该系统每周一次鼻内递送卵清蛋白(OVA),持续3周,可增强OVA诱导的小鼠脾细胞产生干扰素-γ。这种治疗还减弱了OVA诱导的脾细胞释放白细胞介素-4(IL-4)和IL-5,以及OVA敏感的AR模型小鼠血浆中OVA特异性免疫球蛋白E的产生。因此,含变应原的HVJ-E可能对AR的无创治疗有用。

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