Momburg F, Hengel H
Deutsches Krebsforschungszentrum, Department of Molecular Immunology, 69120 Heidelberg, Germany.
Curr Top Microbiol Immunol. 2002;269:57-74. doi: 10.1007/978-3-642-59421-2_4.
In this chapter, mechanisms are reviewed that viruses use to inhibit the function of the peptide transporter associated with antigen processing (TAP), which translocates cytosolic peptides into the endoplasmic reticulum (ER) for binding to MHC class I molecules. Although some DNA viruses, such as adenovirus or EBV, downmodulate TAP expression on the transcriptional level, members of the alpha and beta subfamily of herpesviruses, such as herpes simplex virus (HSV) and human cytomegalovirus (HCMV), express proteins that bind to TAP and interfere with peptide translocation. The modes of action of the HSV-encoded cytosolic TAP inhibitor ICP47 and the HCMV-encoded ER-resident TAP inhibitor gpUS6 are discussed in detail. Viral interference with antigen presentation through TAP inhibition is not only relevant for the immunobiology of persistent viral infections but also contributes to the understanding of the translocation mechanism utilized by the ATP-binding cassette transporter TAP.
在本章中,我们将综述病毒用于抑制与抗原加工相关的肽转运体(TAP)功能的机制,TAP可将胞质肽转运至内质网(ER)以与MHC I类分子结合。尽管一些DNA病毒,如腺病毒或EB病毒,在转录水平下调TAP表达,但疱疹病毒α和β亚科的成员,如单纯疱疹病毒(HSV)和人巨细胞病毒(HCMV),会表达与TAP结合并干扰肽转运的蛋白质。我们将详细讨论HSV编码的胞质TAP抑制剂ICP47和HCMV编码的内质网驻留TAP抑制剂gpUS6的作用方式。病毒通过抑制TAP对抗原呈递的干扰不仅与持续性病毒感染的免疫生物学相关,也有助于理解ATP结合盒转运体TAP所利用的转运机制。