Webb Tonya J Roberts, Litavecz Roberta A, Khan Masood A, Du Wenjun, Gervay-Hague Jacquelyn, Renukaradhya Gourapura J, Brutkiewicz Randy R
Department of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, IN 46202-5181, USA.
Eur J Immunol. 2006 Oct;36(10):2595-600. doi: 10.1002/eji.200636024.
Vaccinia virus (VV) has been most commonly used as the vaccine to protect individuals against the causative agent of smallpox (variola virus), but it also uses a number of strategies meant to evade or blunt the host's antiviral immune response. Natural killer T (NKT) cells are a subset of immunoregulatory CD1d-restricted T lymphocytes believed to bridge the innate and adaptive immune responses. It is shown here that the VV-encoded molecules, B1R and H5R, play a role in the ability of VV to inhibit CD1d-mediated antigen presentation to NKT cells. These are the first poxvirus-encoded molecules identified that can play such a role in the evasion of an important component of the innate immune response.
痘苗病毒(VV)最常被用作疫苗来保护个体免受天花病原体(天花病毒)的侵害,但它也采用了多种策略来逃避或削弱宿主的抗病毒免疫反应。自然杀伤T(NKT)细胞是免疫调节性CD1d限制性T淋巴细胞的一个亚群,被认为可连接先天性免疫反应和适应性免疫反应。本文表明,痘苗病毒编码的分子B1R和H5R在痘苗病毒抑制CD1d介导的向NKT细胞呈递抗原的能力中发挥作用。这些是首次鉴定出的在逃避先天性免疫反应重要组成部分中起此类作用的痘病毒编码分子。