Suppression of costimulation by human cytomegalovirus promotes evasion of cellular immune defenses
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
Grant support
MR/P001602/1
Medical Research Council - United Kingdom
108070
Wellcome Trust - United Kingdom
210688/Z/18/Z
Wellcome Trust - United Kingdom
G1000236
Medical Research Council - United Kingdom
WT090323MA
Wellcome Trust - United Kingdom
MR/L018373/1
Medical Research Council - United Kingdom
MC_UU_12014/12
Medical Research Council - United Kingdom
MC_UU_12014/3
Medical Research Council - United Kingdom
HS-14-11
HCRW_ - United Kingdom
101835
Wellcome Trust - United Kingdom
MR/L008734/1
Medical Research Council - United Kingdom
PubMed
29691324
PubMed Central
PMC5948980
DOI
10.1073/pnas.1720950115
PII: 1720950115
Knihovny.cz E-resources
- Keywords
- CD58, CTLs, NK cells, human cytomegalovirus, immune modulation,
- MeSH
- Immunity, Cellular * MeSH
- Killer Cells, Natural immunology pathology MeSH
- CD8-Positive T-Lymphocytes immunology pathology MeSH
- Cytomegalovirus Infections genetics immunology pathology MeSH
- Cytomegalovirus genetics immunology MeSH
- Immune Evasion * MeSH
- Humans MeSH
- Viral Fusion Proteins genetics immunology MeSH
- Cell Line, Transformed MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Viral Fusion Proteins MeSH
- UL148 protein, human cytomegalovirus MeSH Browser
CD58 is an adhesion molecule that is known to play a critical role in costimulation of effector cells and is intrinsic to immune synapse structure. Herein, we describe a virally encoded gene that inhibits CD58 surface expression. Human cytomegalovirus (HCMV) UL148 was necessary and sufficient to promote intracellular retention of CD58 during HCMV infection. Blocking studies with antagonistic anti-CD58 mAb and an HCMV UL148 deletion mutant (HCMV∆UL148) with restored CD58 expression demonstrated that the CD2/CD58 axis was essential for the recognition of HCMV-infected targets by CD8+ HCMV-specific cytotoxic T lymphocytes (CTLs). Further, challenge of peripheral blood mononuclear cells ex vivo with HCMV∆UL148 increased both CTL and natural killer (NK) cell degranulation against HCMV-infected cells, including NK-driven antibody-dependent cellular cytotoxicity, showing that UL148 is a modulator of the function of multiple effector cell subsets. Our data stress the effect of HCMV immune evasion functions on shaping the immune response, highlighting the capacity for their potential use in modulating immunity during the development of anti-HCMV vaccines and HCMV-based vaccine vectors.
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