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Cytomegalovirus phosphoprotein 150 (pp150) and other CMV-derived peptides presented on HLA class I (CMV pp150/HLA-I complex)

Target
CMV pp150/HLA-I complex
Molecular classification
Peptide-MHC complex, Viral antigen, Tegument protein
01

Overview

Cytomegalovirus (CMV) phosphoprotein 150 (pp150), encoded by the UL32 gene, is a major tegument protein essential for the stabilization of the viral capsid during maturation and egress (UniProt P06473). In infected cells, pp150 and other viral proteins like pp65 and IE1 are processed into short peptides and presented on the cell surface by Human Leukocyte Antigen (HLA) class I molecules. This peptide-HLA complex serves as a critical target for the host's immune system, specifically for CD8+ cytotoxic T-lymphocytes (CTLs), which recognize these epitopes to eliminate infected cells (PubMed: 31110034). Therapeutic strategies targeting these complexes include adoptive cell transfer of CMV-specific T-cells and the development of TCR-engineered T-cells (TCR-T) designed to recognize specific pp150 epitopes, such as those presented by HLA-A*02:01. Additionally, multi-antigen vaccines like Triplex utilize pp150 to induce robust cellular immunity in transplant recipients (PubMed: 28655821). These interventions are primarily aimed at preventing or treating CMV-related complications in immunocompromised individuals, such as hematopoietic stem cell or solid organ transplant recipients. By enhancing the cellular immune response against these viral antigens, these therapies help control viral replication and reduce the risk of clinical CMV disease.

Other names
CMV UL32CMV pUL32Cytomegalovirus phosphoprotein 150CMV peptide-MHC class I complexCMV tegument protein pp150
02

Mechanism of action

Recognition of the viral peptide-HLA complex by the T-cell receptor (TCR) on CD8+ cytotoxic T-lymphocytes, triggering the release of perforin and granzymes to induce apoptosis in CMV-infected cells.

03

Biological functions

Viral capsid maturationViral egressAntigen presentationImmune recognitionT-cell activation
04

Disease associations

Cytomegalovirus infectionPost-transplant lymphoproliferative disorderCongenital cytomegalovirus infectionInfection in immunocompromised patients
05

Safety considerations

Graft-versus-host disease (GvHD) in allogeneic settingsCytokine release syndrome (CRS)Immune evasion via viral downregulation of HLA class IOff-target toxicity due to TCR cross-reactivity
06

Interacting drugs

Triplex vaccine

3 more in the full profile.

07

Biomarkers

HLA-A*02:01 genotypeCMV serostatusCMV DNAemia (viral load)CMV-specific T-cell frequency (ELISPOT/Tetramer staining)

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