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Flt3配体cDNA与CpG寡脱氧核苷酸联合作为鼻腔佐剂可在老年小鼠中引发针对肺炎链球菌的保护性分泌型IgA免疫。

A combination of Flt3 ligand cDNA and CpG oligodeoxynucleotide as nasal adjuvant elicits protective secretory-IgA immunity to Streptococcus pneumoniae in aged mice.

作者信息

Fukuyama Yoshiko, King Janice D, Kataoka Kosuke, Kobayashi Ryoki, Gilbert Rebekah S, Hollingshead Susan K, Briles David E, Fujihashi Kohtaro

机构信息

Department of Pediatric Dentistry, Immunobiology Vaccine Center, Institute of Oral Health Research, University of Alabama at Birmingham, AL 35294-0007, USA.

出版信息

J Immunol. 2011 Feb 15;186(4):2454-61. doi: 10.4049/jimmunol.1002837. Epub 2011 Jan 17.

Abstract

Our previous study showed that a combination of a plasmid-expressing Flt3 ligand (pFL) and CpG oligodeoxynucleotides (CpG ODN) as a combined nasal adjuvant elicited mucosal immune responses in aged (2-y-old) mice. In this study, we investigated whether a combination of pFL and CpG ODN as a nasal adjuvant for a pneumococcal surface protein A (PspA) would enhance PspA-specific secretory-IgA Ab responses, which could provide protective mucosal immunity against Streptococcus pneumoniae infection in aged mice. Nasal immunization with PspA plus a combination of pFL and CpG ODN elicited elevated levels of PspA-specific secretory-IgA Ab responses in external secretions and plasma in both young adult and aged mice. Significant levels of PspA-specific CD4(+) T cell proliferative and PspA-induced Th1- and Th2- type cytokine responses were noted in nasopharyngeal-associated lymphoreticular tissue, cervical lymph nodes, and spleen of aged mice, which were equivalent to those in young adult mice. Additionally, increased numbers of mature-type CD8, CD11b-expressing dendritic cells were detected in mucosal inductive and effector lymphoid tissues of aged mice. Importantly, aged mice given PspA plus a combination of pFL and CpG ODN showed protective immunity against nasal S. pneumoniae colonization. These results demonstrate that nasal delivery of a combined DNA adjuvant offers an attractive possibility for protection against S. pneumoniae in the elderly.

摘要

我们之前的研究表明,表达Flt3配体的质粒(pFL)与CpG寡脱氧核苷酸(CpG ODN)联合作为鼻腔佐剂可在老年(2岁)小鼠中引发黏膜免疫反应。在本研究中,我们调查了pFL与CpG ODN联合作为肺炎球菌表面蛋白A(PspA)的鼻腔佐剂是否会增强PspA特异性分泌型IgA抗体反应,这可为老年小鼠提供针对肺炎链球菌感染的保护性黏膜免疫。用PspA加pFL与CpG ODN联合进行鼻腔免疫,在年轻成年和老年小鼠的外分泌液和血浆中均引发了PspA特异性分泌型IgA抗体反应水平的升高。在老年小鼠的鼻咽相关淋巴组织、颈淋巴结和脾脏中,观察到显著水平的PspA特异性CD4(+) T细胞增殖以及PspA诱导的Th1型和Th2型细胞因子反应,这些反应与年轻成年小鼠相当。此外,在老年小鼠的黏膜诱导和效应淋巴组织中检测到表达成熟型CD8、CD11b的树突状细胞数量增加。重要的是,给予PspA加pFL与CpG ODN联合的老年小鼠对鼻腔肺炎链球菌定植表现出保护性免疫。这些结果表明,鼻腔递送联合DNA佐剂为老年人预防肺炎链球菌感染提供了一种有吸引力的可能性。

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