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使用紧密连接蛋白 4 靶向的黏膜疫苗接种。

Mucosal vaccination using claudin-4-targeting.

机构信息

Laboratory of Bio-Functional Molecular Chemistry, Graduate School of Pharmaceutical Sciences, Osaka University, Suita, Osaka 565-0871, Japan.

出版信息

Biomaterials. 2010 Jul;31(20):5463-71. doi: 10.1016/j.biomaterials.2010.03.047.

Abstract

Mucosa-associated lymphoid tissue (MALT) plays pivotal roles in mucosal immune responses. Efficient delivery of antigens to MALT is a critical issue for the development of mucosal vaccines. Although claudin-4 is preferentially expressed in MALT in the gut, a claudin-4-targeting approach for mucosal vaccination has never been developed. In the present study, we found that claudin-4 is expressed in nasal MALT, and we prepared a fusion protein of ovalbumin (OVA) as a model antigen with a claudin-4-binder, the C-terminal fragment of Clostridium perfringens enterotoxin (C-CPE) (OVA-C-CPE). Nasal immunization with OVA-C-CPE, but not a mixture of OVA and C-CPE, induced the production of OVA-specific serum IgG and nasal, vaginal and fecal IgA. Deletion of the claudin-4-binding region in OVA-C-CPE attenuated the induction of the immune responses. OVA-C-CPE immunization activated both Th1 and Th2 responses, and nasal immunization with OVA-C-CPE showed anti-tumor activity in mice inoculated with OVA-expressing thymoma cells. These results indicate that the claudin-4-targeting may be a potent strategy for nasal vaccination.

摘要

黏膜相关淋巴组织 (MALT) 在黏膜免疫反应中发挥关键作用。将抗原有效递送至 MALT 是黏膜疫苗开发的关键问题。虽然 Claudin-4 在肠道的 MALT 中优先表达,但从未开发出针对 Claudin-4 的黏膜疫苗接种方法。在本研究中,我们发现 Claudin-4 在鼻黏膜相关淋巴组织中表达,并制备了卵清蛋白 (OVA) 作为模型抗原与 Claudin-4 结合物、产气荚膜梭菌肠毒素 C 端片段 (C-CPE) 的融合蛋白 (OVA-C-CPE)。鼻内免疫接种 OVA-C-CPE 而非 OVA 和 C-CPE 的混合物可诱导产生 OVA 特异性血清 IgG 和鼻、阴道和粪便 IgA。在 OVA-C-CPE 中删除 Claudin-4 结合区可减弱免疫反应的诱导。OVA-C-CPE 免疫接种可激活 Th1 和 Th2 反应,并且用 OVA-C-CPE 进行鼻内免疫接种可在接种表达 OVA 的胸腺瘤细胞的小鼠中显示抗肿瘤活性。这些结果表明 Claudin-4 靶向可能是鼻内疫苗接种的有效策略。

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