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先天免疫定义了抗病毒 T 细胞限制持续性感染的能力。

Innate immunity defines the capacity of antiviral T cells to limit persistent infection.

机构信息

Immunology and Virology Program, Centre for Ophthalmology and Visual Science, University Department of Medicine, University of Western Australia, Nedlands, Western Australia 6009, Australia.

出版信息

J Exp Med. 2010 Jun 7;207(6):1333-43. doi: 10.1084/jem.20091193. Epub 2010 May 31.

Abstract

Effective immunity requires the coordinated activation of innate and adaptive immune responses. Natural killer (NK) cells are central innate immune effectors, but can also affect the generation of acquired immune responses to viruses and malignancies. How NK cells influence the efficacy of adaptive immunity, however, is poorly understood. Here, we show that NK cells negatively regulate the duration and effectiveness of virus-specific CD4+ and CD8+ T cell responses by limiting exposure of T cells to infected antigen-presenting cells. This impacts the quality of T cell responses and the ability to limit viral persistence. Our studies provide unexpected insights into novel interplays between innate and adaptive immune effectors, and define the critical requirements for efficient control of viral persistence.

摘要

有效的免疫需要先天和适应性免疫反应的协调激活。自然杀伤 (NK) 细胞是先天免疫效应的核心,但也可以影响对病毒和恶性肿瘤的获得性免疫反应的产生。然而,NK 细胞如何影响适应性免疫的疗效还知之甚少。在这里,我们表明 NK 细胞通过限制 T 细胞与感染的抗原呈递细胞接触来负调节病毒特异性 CD4+和 CD8+T 细胞反应的持续时间和有效性。这会影响 T 细胞反应的质量和限制病毒持续存在的能力。我们的研究为先天和适应性免疫效应器之间的新相互作用提供了意想不到的见解,并确定了有效控制病毒持续存在的关键要求。

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