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经肺部 DNA 免疫接种后,高效产生粘膜和系统抗原特异性 CD8+ T 细胞应答。

Efficient generation of mucosal and systemic antigen-specific CD8+ T-cell responses following pulmonary DNA immunization.

机构信息

Division of Viral Pathogenesis, Beth Israel Deaconess Medical Center, Harvard Medical School, 330 Brookline Avenue, Boston, MA 02215, USA.

出版信息

J Virol. 2010 Jun;84(11):5764-74. doi: 10.1128/JVI.02202-09. Epub 2010 Mar 24.

Abstract

Although mucosal CD8(+) T-cell responses are important in combating mucosal infections, the generation of such immune responses by vaccination remains problematic. In the present study, we evaluated the ability of plasmid DNA to induce local and systemic antigen-specific CD8(+) T-cell responses after pulmonary administration. We show that the pulmonary delivery of plasmid DNA formulated with polyethyleneimine (PEI-DNA) induced robust systemic CD8(+) T-cell responses that were comparable in magnitude to those generated by intramuscular (i.m.) immunization. Most importantly, we observed that the pulmonary delivery of PEI-DNA elicited a 10-fold-greater antigen-specific CD8(+) T-cell response in lungs and draining lymph nodes of mice than that of i.m. immunization. The functional evaluation of these pulmonary CD8(+) T cells revealed that they produced type I cytokines, and pulmonary immunization with PEI-DNA induced lung-associated antigen-specific CD4(+) T cells that produced higher levels of interleukin-2 than those induced by i.m. immunization. Pulmonary PEI-DNA immunization also induced CD8(+) T-cell responses in the gut and vaginal mucosa. Finally, pulmonary, but not i.m., plasmid DNA vaccination protected mice from a lethal recombinant vaccinia virus challenge. These findings suggest that pulmonary PEI-DNA immunization might be a useful approach for immunizing against pulmonary pathogens and might also protect against infections initiated at other mucosal sites.

摘要

虽然黏膜 CD8(+) T 细胞应答对于抵抗黏膜感染很重要,但疫苗接种产生这种免疫应答仍然存在问题。在本研究中,我们评估了质粒 DNA 经肺部给药后产生局部和全身抗原特异性 CD8(+) T 细胞应答的能力。我们发现,用聚乙烯亚胺(PEI-DNA)配制的质粒 DNA 经肺部给药可诱导出强大的全身 CD8(+) T 细胞应答,其强度可与肌肉内(i.m.)免疫产生的应答相媲美。最重要的是,我们观察到,与 i.m. 免疫相比,PEI-DNA 的肺部给药在肺部和引流淋巴结中引发了 10 倍更强的抗原特异性 CD8(+) T 细胞应答。对这些肺部 CD8(+) T 细胞的功能评估表明,它们产生了 I 型细胞因子,并且 PEI-DNA 肺部免疫诱导了肺部相关抗原特异性 CD4(+) T 细胞,这些细胞产生的白细胞介素-2 水平高于 i.m. 免疫诱导的水平。肺部 PEI-DNA 免疫还诱导了肠道和阴道黏膜中的 CD8(+) T 细胞应答。最后,肺部而非肌肉内的质粒 DNA 疫苗接种可保护小鼠免受致命重组痘苗病毒的挑战。这些发现表明,肺部 PEI-DNA 免疫可能是一种针对肺部病原体的有效免疫接种方法,也可能对其他黏膜部位引发的感染提供保护。

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