| Literature DB >> 29374075 |
Blake F Frey1, Jiansheng Jiang2, Yongjun Sui3, Lisa F Boyd2, Bin Yu4, Gwen Tatsuno4, Rolf Billeskov1, Shahram Solaymani-Mohammadi1, Phillip W Berman4, David H Margulies2, Jay A Berzofsky1.
Abstract
Unlike cytosolic processing and presentation of viral Ags by virus-infected cells, Ags first expressed in infected nonprofessional APCs, such as CD4+ T cells in the case of HIV, are taken up by dendritic cells and cross-presented. This generally requires entry through the endocytic pathway, where endosomal proteases have first access for processing. Thus, understanding virus escape during cross-presentation requires an understanding of resistance to endosomal proteases, such as cathepsin S (CatS). We have modified HIV-1MN gp120 by mutating a key CatS cleavage site (Thr322Thr323) in the V3 loop of the immunodominant epitope IGPGRAFYTT to IGPGRAFYVV to prevent digestion. We found this mutation to facilitate cross-presentation and provide evidence from MHC binding and X-ray crystallographic structural studies that this results from preservation of the epitope rather than an increased epitope affinity for the MHC class I molecule. In contrast, when the protein is expressed by a vaccinia virus in the cytosol, the wild-type protein is immunogenic without this mutation. These proof-of-concept results show that a virus like HIV, infecting predominantly nonprofessional presenting cells, can escape T cell recognition by incorporating a CatS cleavage site that leads to destruction of an immunodominant epitope when the Ag undergoes endosomal cross-presentation.Entities:
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Year: 2018 PMID: 29374075 PMCID: PMC5890335 DOI: 10.4049/jimmunol.1701523
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422