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The 65 kDa lower matrix phosphoprotein, commonly known as pp65 or tegument protein UL83, is the most abundant structural protein of the Human Cytomegalovirus (HCMV) tegument. It plays a critical role in the early stages of viral infection by modulating the host's innate immune response, specifically by inhibiting the induction of interferon-stimulated genes and blocking natural killer cell activation [1][3]. pp65 is highly immunodominant, making it the primary target for the host's cytotoxic T-lymphocyte (CTL) response during natural infection [2]. In clinical settings, the detection of pp65 within white blood cells, known as the pp65 antigenemia assay, is a gold-standard diagnostic tool for identifying active CMV replication in immunocompromised patients [5]. From a therapeutic perspective, pp65 is a major focus for vaccine development and adoptive immunotherapy, where CMV-specific T cells are expanded ex vivo to restore immunity in transplant recipients [4]. Emerging research also investigates the presence of pp65 in certain malignancies, such as glioblastoma, as a potential target for tumor-directed immunotherapy [6]. Citations: [1] UniProt (P06725); [2] PubMed (PMID: 10823859); [3] PubMed (PMID: 24478440); [4] ClinicalTrials.gov (NCT03394781); [5] PubMed (PMID: 15103403); [6] PubMed (PMID: 23143591).
Targeting as an immunodominant antigen for vaccine-induced or adoptive T-cell mediated cytotoxicity against HCMV-infected cells.
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