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BST-2/tetherin: Structural biology, viral antagonism, and immunobiology of a potent host antiviral factor

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MOLECULAR IMMUNOLOGY
卷 54, 期 2, 页码 132-139

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PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.molimm.2012.11.008

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Innate immunity; Tetherin; Virology; Interferon; Plasmacytoid dendritic cells; Antiviral state

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BST-2 (also known as tetherin, CD317, or HM1.24) was first described as a potent interferon-inducible host antiviral factor nearly five years ago. Since that time, numerous reports have been published regarding the antiviral activity and immunological properties of this protein. BST-2 blocks viral replication by inhibiting enveloped virus budding from the surface of infected cells. To counteract this, most viruses have developed strategies to antagonize BST-2, each employing a unique mechanism. In this review, we summarize the antiviral function, structural biology and immunobiology of BST-2. Taken together, our current understanding of BST-2 suggests potential avenues as well as challenges to exploiting its action in the development of broad spectrum antiviral treatments. (C) 2012 Elsevier Ltd. All rights reserved.

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