Campbell Family Institute for Breast Cancer Research, Ontario Cancer Institute, University Health Network, Toronto, ON, Canada M5G 2C1.
Proc Natl Acad Sci U S A. 2012 Jan 24;109(4):1210-5. doi: 10.1073/pnas.1118834109. Epub 2011 Dec 13.
Infections with HIV, hepatitis B virus, and hepatitis C virus can turn into chronic infections, which currently affect more than 500 million patients worldwide. It is generally thought that virus-mediated T-cell exhaustion limits T-cell function, thus promoting chronic disease. Here we demonstrate that natural killer (NK) cells have a negative impact on the development of T-cell immunity by using the murine lymphocytic choriomeningitis virus. NK cell-deficient (Nfil3(-/-), E4BP4(-/-)) mice exhibited a higher virus-specific T-cell response. In addition, NK cell depletion caused enhanced T-cell immunity in WT mice, which led to rapid virus control and prevented chronic infection in lymphocytic choriomeningitis virus clone 13- and reduced viral load in DOCILE-infected animals. Further experiments showed that NKG2D triggered regulatory NK cell functions, which were mediated by perforin, and limited T-cell responses. Therefore, we identified an important role of regulatory NK cells in limiting T-cell immunity during virus infection.
HIV、乙型肝炎病毒和丙型肝炎病毒感染可转为慢性感染,目前全球有超过 5 亿患者受到影响。一般认为,病毒介导的 T 细胞耗竭限制了 T 细胞功能,从而促进了慢性疾病的发生。在这里,我们通过使用鼠类淋巴细胞性脉络丛脑膜炎病毒证明了自然杀伤 (NK) 细胞对 T 细胞免疫的发展具有负面影响。NK 细胞缺陷(Nfil3(-/-)、E4BP4(-/-))小鼠表现出更高的病毒特异性 T 细胞反应。此外,NK 细胞耗竭导致 WT 小鼠的 T 细胞免疫增强,从而导致病毒迅速得到控制,并防止了淋巴细胞性脉络丛脑膜炎病毒克隆 13 的慢性感染和降低了 DOCILE 感染动物的病毒载量。进一步的实验表明,NKG2D 触发了由穿孔素介导的调节性 NK 细胞功能,从而限制了 T 细胞反应。因此,我们确定了调节性 NK 细胞在病毒感染期间限制 T 细胞免疫中的重要作用。