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Human papillomavirus 18 E7 antigen peptide–HLA-DRB1*09:01 complex

Molecular classification
Antigen-peptide/MHC class II complex, Antigen presentation molecule complex, Other
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Overview

The “Human papillomavirus 18 E7 antigen peptide–HLA-DRB1*09:01 complex” consists of a peptide fragment derived from the E7 oncoprotein of HPV18, bound to the major histocompatibility complex (MHC) class II receptor HLA-DRB1*09:01. This complex is recognized by CD4+ T cells, enabling immune recognition and elimination of HPV18-infected or transformed cells. The E7 protein is a central viral oncoprotein driving disruption of cell cycle control, facilitating cancer progression in persistent HPV infections[1][4]. Peptides derived from E7 are frequently studied as targets in therapeutic vaccines, as their presentation on specific HLA molecules (e.g., DRB1*09:01) is key to initiating robust, antigen-specific T-cell responses crucial for immunotherapy against HPV-associated malignancies[2][4][7]. The complex serves as a molecular target in research and experimental therapies for cervical and other HPV-related cancers, specifically in immunological patient subgroups defined by their HLA type[2][3][4][7].

Other names
HPV18 E7 peptide/HLA-DRB1*09:01 complexHPV18 E7-HLA-DRB1*09:01HPV18 E7-derived T-cell epitope/HLA-DRB1*09:01
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Mechanism of action

Vaccines induce E7 peptide presentation by HLA-DRB1*09:01, stimulating antigen-specific CD4+ T cells to mount immune responses against HPV-infected or transformed (cancer) cells[2][4]. T cells recognize the peptide–MHC complex, leading to targeted immune-mediated destruction of HPV-positive cancer cells.

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Biological functions

Immune response initiation (T-cell activation)Antigen presentationAdaptive immunity (CD4+ T cell stimulation)Cancer immunosurveillance
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Disease associations

Cancer (oncogenic HPV, cervical and other anogenital cancers)Infection (HPV infection/clearance)Other (autoimmunity rare, context dependent)
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Safety considerations

Potential for off-target T-cell responses or autoimmunity (rare)[2][4].Risk of immune-mediated tissue damage, though generally low in peptide vaccine settings.Limited efficacy in patients lacking the relevant HLA-DRB1*09:01 allele.Immunogenicity issues (variable antigen processing/presentation).
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Interacting drugs

No classical small-molecule drugs. However, investigational peptide-based therapeutic vaccines and immunotherapies target the E7/HLA complex[2][4].

2 more in the full profile.

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Biomarkers

Presence of HPV18 E7-specific CD4+ T-cell responsesHLA-DRB1*09:01 genotype (patient selection for vaccine efficacy)Tumor/lesion HPV18 positivity

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