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小鼠中肺炎球菌表面蛋白A的经皮免疫接种。

Transcutaneous immunization with pneumococcal surface protein A in mice.

作者信息

Nagano Hiromi, Kawabata Masaki, Sugita Gen, Tsuruhara Akitoshi, Ohori Junichiro, Jimura Tomohiro, Miyashita Keiichi, Kurono Yuichi, Tomonaga Kazuhiro, Briles David E, Fujihashi Kohtaro

机构信息

Immunobiology, Vaccine Center, Institute of Oral Health Research, University of Alabama at Birmingham, Birmingham, Alabama, U.S.A.

Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan.

出版信息

Laryngoscope. 2018 Mar;128(3):E91-E96. doi: 10.1002/lary.26971. Epub 2017 Dec 11.

Abstract

OBJECTIVE

Pneumococcal infection caused by Streptococcus pneumoniae is a major upper respiratory tract disease that causes severe illness and mortality. Therefore, it is important to develop safe and effective vaccines to prevent pneumococcal infections. The goal of the study was to investigate the effectiveness of transcutaneous immunization (TCI) for induction of pneumococcal surface protein A (PspA) responses in the upper respiratory tract.

METHODS

C57BL/6 mice were transcutaneously immunized with 1 μg of PspA and 2 μg of cholera toxin (CT) six times at weekly intervals and compared with transcutaneously treated controls (PBS alone/PspA alone/CT alone). Two weeks after the final immunization, nasal washes (NWs), saliva, and plasma samples were collected and subjected to a PspA-specific ELISA. Three weeks after the final immunization, mice were challenged with S. pneumoniae strain EF3030, and the numbers of CFUs in NWs and nasal passages (NPs) were determined.

RESULTS

Higher levels of PspA-specific IgM, IgG, and IgA Abs were noted in plasma of TCI with PspA plus CT compared with controls. Transcutaneous immunization mice also had significantly increased PspA-specific S-IgA Ab responses in NWs and saliva and, importantly, showed significantly lower numbers of bacteria CFUs in NWs and NPs compared with controls.

CONCLUSION

These results show that TCI with PspA plus CT induces antigen-specific mucosal and systemic immune responses. This suggests that this method is an effective mucosal immunization strategy for induction of protective pneumococcal-specific Ab responses in blockade of S. pneumoniae colonization of the nasal cavity.

LEVEL OF EVIDENCE

NA. Laryngoscope, 128:E91-E96, 2018.

摘要

目的

肺炎链球菌引起的肺炎球菌感染是一种主要的上呼吸道疾病,可导致严重疾病和死亡。因此,开发安全有效的疫苗来预防肺炎球菌感染非常重要。本研究的目的是调查经皮免疫(TCI)在上呼吸道诱导肺炎球菌表面蛋白A(PspA)反应的有效性。

方法

将1μg PspA和2μg霍乱毒素(CT)每周经皮免疫C57BL/6小鼠6次,并与经皮处理的对照组(单独使用PBS/单独使用PspA/单独使用CT)进行比较。末次免疫后两周,收集鼻洗液(NWs)、唾液和血浆样本,并进行PspA特异性酶联免疫吸附测定(ELISA)。末次免疫后三周,用肺炎链球菌EF3030菌株攻击小鼠,并测定NWs和鼻腔(NPs)中的菌落形成单位(CFUs)数量。

结果

与对照组相比,PspA加CT经皮免疫的小鼠血浆中PspA特异性IgM、IgG和IgA抗体水平更高。经皮免疫的小鼠在NWs和唾液中的PspA特异性分泌型IgA(S-IgA)抗体反应也显著增加,重要的是,与对照组相比,NWs和NPs中的细菌CFUs数量显著降低。

结论

这些结果表明,PspA加CT经皮免疫可诱导抗原特异性黏膜和全身免疫反应。这表明该方法是一种有效的黏膜免疫策略,可在阻断肺炎链球菌鼻腔定植中诱导保护性肺炎球菌特异性抗体反应。

证据水平

无。《喉镜》,2018年,第128卷:E91-E96页。

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