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通过母体鼻内接种肺炎球菌表面蛋白A(PspA)预防全身性致死性肺炎球菌感染。

Protection against systemic fatal pneumococcal infection by maternal intranasal immunization with pneumococcal surface protein A (PspA).

作者信息

Katsurahara Toshiki, Hotomi Muneki, Yamauchi Kazuma, Billal Dewan S, Yamanaka Noboru

机构信息

Department of Otolaryngology-Head and Neck Surgery, Wakayama Medical University, 811-1 Kimiidera, Wakayama, 641-8509, Japan.

出版信息

J Infect Chemother. 2008 Dec;14(6):393-8. doi: 10.1007/s10156-008-0647-7. Epub 2008 Dec 17.

Abstract

Streptococcus pneumoniae is a leading causative pathogen responsible for various types of bacterial infectious diseases in children. The aim of this study was to evaluate the protection conferred against fatal pneumococcal infections during infancy by maternal intranasal immunization with pneumococcal surface protein A (PspA). Four-week-old female BALB/c mice were immunized with PspA mixed with, or without, cholera toxin B (CTB) intranasally twice a week for 3 weeks. After the final immunization, they were mated with male mice to obtain offspring. Offspring at 10 days old were intraperitoneally inoculated with a pneumococcus strain, TIGR4, serotype 4. After the infections their survival periods were monitored. Anti-PspA-specific IgG antibody was induced in sera and breast milk at birth and maintained for 14 days during nursing periods in the PspA-immunized mother mice. At birth, offspring delivered from PspA-immunized mother mice had levels of anti-PspA-specific IgG antibody in sera same to those in their mothers on the day of birth. The survival times to death of offspring delivered from PspA-immunized mother mice after systemic fatal pneumococcal infections were significantly extended compared to those of controls. These findings suggest that maternal intranasal immunization with PspA could be an attractive procedure to employ against pneumococcal infections in early childhood.

摘要

肺炎链球菌是导致儿童各类细菌性传染病的主要致病病原体。本研究的目的是评估通过鼻内接种肺炎球菌表面蛋白A(PspA)对母体进行免疫,从而为婴儿期致命性肺炎球菌感染提供的保护作用。4周龄雌性BALB/c小鼠每周鼻内接种两次PspA(添加或不添加霍乱毒素B(CTB)),持续3周。末次免疫后,将其与雄性小鼠交配以获得后代。10日龄的后代腹腔注射肺炎球菌菌株TIGR4(血清型4)。感染后监测它们的存活期。PspA免疫的母鼠在出生时血清和母乳中诱导产生抗PspA特异性IgG抗体,并在哺乳期维持14天。出生时,PspA免疫的母鼠所产后代血清中抗PspA特异性IgG抗体水平与其母亲出生当天的水平相同。与对照组相比,全身性致命肺炎球菌感染后,PspA免疫的母鼠所产后代的死亡存活时间显著延长。这些发现表明,对母体进行鼻内接种PspA可能是预防幼儿肺炎球菌感染的一种有吸引力的方法。

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