首页> 外文OA文献 >Nasal delivery of Japanese cedar pollen Cryj1 by using self-gelling immunostimulatory DNA for effective induction of immune responses in mice.
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Nasal delivery of Japanese cedar pollen Cryj1 by using self-gelling immunostimulatory DNA for effective induction of immune responses in mice.

机译:日本雪松花粉Cryj1的鼻腔递送通过使用自胶凝免疫刺激DNA有效诱导小鼠的免疫应答。

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摘要

To develop an immunotherapeutic vaccine for treatment of allergic rhinitis, we developed a controlled release formulation of Cryj1, a major Japanese cedar pollen allergen, with immunostimulatory potency. Two sets of hexapod-like structured DNA (hexapodna) were prepared using six oligodeoxynucleotides (ODNs) each, including ODNs with an unmethylated cytosine-phosphate-guanine (CpG) sequence (CpG motif), to obtain an immunostimulatory DNA hydrogel (sDNA hydrogel). A non-immunostimulatory DNA hydrogel (nsDNA hydrogel) was also prepared using ODNs with no CpG motifs. The sDNA hydrogel was more effective than its components or the nsDNA hydrogel for production of interleukin (IL)-12 after addition to murine macrophage-like RAW264.7 cells or after intranasal administration to mice. Then, a Cryj1-loaded sDNA hydrogel (Cryj1/sDNA hydrogel) formulation was prepared by mixing solutions containing both Cryj1 and hexapodna. Cryj1 was slowly released from the sDNA hydrogel in phosphate-buffed saline. After intranasal administration of the fluorescein isothiocyanate (FITC)-labeled Cryj1/sDNA hydrogel in mice, FITC-Cryj1 was retained in the nasal cavity for a longer period than FITC-Cryj1 mixed with hexapodna in solution. Intranasal immunization of mice with the Cryj1/sDNA hydrogel resulted in high levels of Cryj1-specific IgG in nasal lavage fluid (NFL), IL-12 and interferon-γ release from spleen cells after re-stimulation with Cryj1 when compared with intranasal immunization with the other formulations examined. These results indicate that the self-gelling immunostimulatory DNA hydrogel is an effective formulation for controlled induction of allergen-specific immune responses.
机译:为了开发用于治疗变应性鼻炎的免疫治疗疫苗,我们开发了Cryj1(一种主要的日本雪松花粉过敏原)的控释制剂,具有免疫刺激力。使用六个寡脱氧核苷酸(ODN)(包括具有未甲基化胞嘧啶-磷酸-鸟嘌呤(CpG)序列(CpG主题)的ODN)制备两组六足体样结构化DNA(hexapodna),以获得免疫刺激性DNA水凝胶(sDNA水凝胶) 。还使用没有CpG图案的ODN制备了非免疫刺激性DNA水凝胶(nsDNA水凝胶)。在向鼠巨噬细胞样RAW264.7细胞中添加或鼻内给予小鼠后,sDNA水凝胶比其组分或nsDNA水凝胶更有效地生产白介素(IL)-12。然后,通过混合同时含有Cryj1和六足虫的溶液来制备载有Cryj1的sDNA水凝胶(Cryj1 / sDNA水凝胶)制剂。 Cryj1在加磷酸盐的盐水中从sDNA水凝胶缓慢释放。鼻腔内注射荧光素异硫氰酸酯(FITC)标记的Cryj1 / sDNA水凝胶后,FITC-Cryj1在鼻腔中的停留时间比在溶液中混有六足蛋白的FITC-Cryj1更长。与Cryj1鼻腔免疫相比,Cryj1 / sDNA水凝胶对小鼠进行鼻内免疫会导致高水平Cryj1特异性IgG在鼻灌洗液(NFL)中,IL-12和干扰素-γ从Cryj1再刺激后从脾细胞中释放出来。检查其他配方。这些结果表明,自胶凝的免疫刺激DNA水凝胶是一种可控的诱导过敏原特异性免疫反应的有效制剂。

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