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Cytomegalovirus immediate-early 1 peptide-major histocompatibility complex (CMV IE-1 pMHC)

Target
CMV IE-1 pMHC
Molecular classification
Peptide-MHC complex, Antigenic complex, Viral protein-MHC complex
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Overview

Cytomegalovirus immediate-early 1 (IE-1) peptide-major histocompatibility complex (pMHC) is a primary immunological target for the cellular immune response against Human Cytomegalovirus (HCMV). The IE-1 protein, encoded by the UL123 gene, is expressed immediately upon viral entry and plays a crucial role in transactivating viral and host genes, making it an early marker of infection (PMID: 15976050). These complexes are formed when proteasome-derived IE-1 peptides are loaded onto MHC Class I molecules in the endoplasmic reticulum and subsequently presented on the cell surface. CD8+ T cells recognize these specific pMHC complexes via their T-cell receptors (TCRs), which is essential for controlling viral latency and reactivation (PMID: 25609814). In clinical development, CMV IE-1 pMHC complexes are targeted by adoptive cell therapies, including donor-derived CMV-specific T cells and TCR-engineered T cells, to treat or prevent CMV disease in immunocompromised patients, such as those undergoing hematopoietic stem cell transplantation (PMID: 30206139). Therapeutic strategies also include vaccines that aim to elicit robust IE-1-specific T-cell responses to provide long-term protection against CMV-related complications.

Other names
HCMV IE1 peptide-HLA complexIE1-MHC complexImmediate-early protein 1 peptide-MHCUL123 peptide-MHCCMV IE1-HLA-A*02:01 complex
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Mechanism of action

Recognition by T-cell receptors (TCRs) on CD8+ cytotoxic T lymphocytes, leading to the targeted lysis of CMV-infected cells and the release of antiviral cytokines like IFN-gamma.

03

Biological functions

Antigen presentationImmune recognitionT-cell activationViral immune evasion
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Disease associations

Cytomegalovirus infectionOpportunistic infectionCongenital cytomegalovirusPost-transplant lymphoproliferative disorder
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Safety considerations

Cross-reactivity with self-antigensCytokine release syndromeGraft-versus-host disease (GvHD)Immune escape via MHC downregulation
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Interacting drugs

CMV-specific T-cell therapy

3 more in the full profile.

07

Biomarkers

HLA-A*02:01 genotypeIE-1 specific T-cell frequencyCMV viral loadHLA-B*07:02 genotype

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