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CpG 预处理增强了抗病毒 T 细胞对巨细胞病毒的免疫应答。

CpG pretreatment enhances antiviral T-cell immunity against cytomegalovirus.

机构信息

Immunology and Virology Program, Centre for Ophthalmology and Visual Science, University of Western Australia, Crawley, WA, Australia.

出版信息

Blood. 2013 Jul 4;122(1):55-60. doi: 10.1182/blood-2012-12-471227. Epub 2013 May 14.

Abstract

Major histocompatibility complex class I-restricted T-cell immunity is essential to control infection with cytomegalovirus (CMV), a clinically important virus that causes significant disease in immunocompromised individuals. Cross-presentation is considered the primary mode of antigen presentation to generate protective antiviral CD8⁺ T-cell immunity. Herpesviruses, including CMV, encode numerous proteins that interfere with direct antigen presentation, leading to the paradigm that T-cell immunity to these pathogens necessitates cross-presentation. However, the antigen presentation requirements needed to generate a protective T-cell response to CMV remain unknown. Here, we show that a fully functional antiviral CD8⁺ T-cell response can be generated in a system where cross-presentation is shut down by pretreatment with CpG. Notably, in this setting, CD8⁺ T cells demonstrate accelerated control of infection, and organ pathology is limited. These data indicate that protective antiviral T-cell immunity to CMV is generated by direct presentation and can be enhanced by pretreatment with CpG.

摘要

主要组织相容性复合体 I 类限制的 T 细胞免疫对于控制巨细胞病毒 (CMV) 的感染至关重要,CMV 是一种具有临床重要性的病毒,可导致免疫功能低下个体发生重大疾病。交叉呈递被认为是产生保护性抗病毒 CD8+T 细胞免疫的主要抗原呈递方式。疱疹病毒,包括 CMV,编码许多干扰直接抗原呈递的蛋白,导致这样的范例,即这些病原体的 T 细胞免疫需要交叉呈递。然而,产生针对 CMV 的保护性 T 细胞反应所需的抗原呈递要求尚不清楚。在这里,我们表明,在 CpG 预处理使交叉呈递失活的系统中,可以产生完全功能性的抗病毒 CD8+T 细胞反应。值得注意的是,在这种情况下,CD8+T 细胞表现出加速的感染控制,并且器官病理学受到限制。这些数据表明,针对 CMV 的保护性抗病毒 T 细胞免疫是通过直接呈递产生的,并且可以通过 CpG 的预处理来增强。

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