Inhibition of CD1d1-mediated antigen presentation by the vaccinia virus B1R and H5R molecules

被引:39
作者
Webb, Tonya J. Roberts
Litavecz, Roberta A.
Khan, Masood A.
Du, Wenjun
Gervay-Hague, Jacquelyn
Renukaradhya, Gourapura J.
Brutkiewicz, Randy R.
机构
[1] Indiana Univ, Sch Med, Dept Microbiol & Immunol, Indianapolis, IN 46202 USA
[2] Indiana Univ, Sch Med, Walther Oncol Ctr, Indianapolis, IN 46202 USA
[3] Walther Canc Inst, Indianapolis, IN USA
[4] Univ Calif Davis, Dept Chem, Davis, CA 95616 USA
关键词
antigen presentation; CD1d; immune evasion; NKT cells; vaccinia virus;
D O I
10.1002/eji.200636024
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:2595 / 2600
页数:6
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