HCMV glycoprotein US6 mediated inhibition of TAP does not affect HLA-E dependent protection of K-562 cells from NK cell lysis (Q78861574)

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17 December 2019

title

HCMV glycoprotein US6 mediated inhibition of TAP does not affect HLA-E dependent protection of K-562 cells from NK cell lysis (English)

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17 December 2019

author name string

Matthias Ulbrecht

1

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17 December 2019

Valeska Hofmeister

2

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17 December 2019

Gülnihål Yüksekdag

3

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17 December 2019

Joachim W Ellwart

4

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17 December 2019

Hartmut Hengel

5

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17 December 2019

Frank Momburg

6

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17 December 2019

Silvia Martinozzi

7

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17 December 2019

Murielle Reboul

8

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17 December 2019

Marika Pla

9

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17 December 2019

Elisabeth H Weiss

10

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17 December 2019

publication date

1 February 2003

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17 December 2019

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17 December 2019

volume

64

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17 December 2019

issue

2

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17 December 2019

page(s)

231-237

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Viral strategies of immune evasion

17 December 2019

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Self class I molecules protect normal cells from lysis mediated by autologous natural killer cells

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Trophoblast class I major histocompatibility complex (MHC) products are resistant to rapid degradation imposed by the human cytomegalovirus (HCMV) gene products US2 and US11.

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Human cytomegalovirus gene products US3 and US6 down-regulate trophoblast class I MHC molecules

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Surface expression of HLA-E, an inhibitor of natural killer cells, enhanced by human cytomegalovirus gpUL40.

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Cutting edge: the human cytomegalovirus UL40 gene product contains a ligand for HLA-E and prevents NK cell-mediated lysis

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Recognition of human histocompatibility leukocyte antigen (HLA)-E complexed with HLA class I signal sequence-derived peptides by CD94/NKG2 confers protection from natural killer cell-mediated lysis

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HLA-E is a major ligand for the natural killer inhibitory receptor CD94/NKG2A

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TAP- and tapasin-dependent HLA-E surface expression correlates with the binding of an MHC class I leader peptide

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7 January 2021

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Identifiers

DOI

1 reference

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17 December 2019

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