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HLA-B locus products resist degradation by the human cytomegalovirus immunoevasin US11.

Cosima Zimmermann | Daniel Kowalewski | Liane Bauersfeld | Andreas Hildenbrand | Carolin Gerke | Magdalena Schwarzmüller | Vu Thuy Khanh Le-Trilling | Stefan Stevanovic | Hartmut Hengel | Frank Momburg | Anne Halenius
PLoS pathogens | 2019

To escape CD8+ T-cell immunity, human cytomegalovirus (HCMV) US11 redirects MHC-I for rapid ER-associated proteolytic degradation (ERAD). In humans, classical MHC-I molecules are encoded by the highly polymorphic HLA-A, -B and -C gene loci. While HLA-C resists US11 degradation, the specificity for HLA-A and HLA-B products has not been systematically studied. In this study we analyzed the MHC-I peptide ligands in HCMV-infected cells. A US11-dependent loss of HLA-A ligands was observed, but not of HLA-B. We revealed a general ability of HLA-B to assemble with β2m and exit from the ER in the presence of US11. Surprisingly, a low-complexity region between the signal peptide sequence and the Ig-like domain of US11, was necessary to form a stable interaction with assembled MHC-I and, moreover, this region was also responsible for changing the pool of HLA-B ligands. Our data suggest a two-pronged strategy by US11 to escape CD8+ T-cell immunity, firstly, by degrading HLA-A molecules, and secondly, by manipulating the HLA-B ligandome.

Pubmed ID: 31527904

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