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Human cytomegalovirus lower matrix phosphoprotein 65 (pp65, UL83) is the most abundant tegument protein in the human cytomegalovirus virion, comprising up to 15% of the virion mass[2][3][4][6]. It is a dominant target for both humoral and cellular immune responses, particularly CD8+ T cells, during natural CMV infection[5][7]. The protein plays a key role in antagonizing the host’s innate immune response—specifically, it prevents IRF-3 (interferon regulatory factor 3) from translocating to the nucleus and blocks early induction of the type I interferon pathway, thereby helping the virus evade immediate antiviral defenses[1][8]. The pp65 antigen is frequently used as a marker of ongoing CMV replication in clinical diagnostics and is a leading candidate for monitoring CMV-specific immunity, especially in transplant recipients[5][6][7]. Although it is essential for immune evasion and virion tegument structure, pp65 is non-essential for CMV replication in vitro, and deletion mutants can still form virions, albeit with structural differences[4]. The listing “Cytomegalovirus phosphoprotein 65 antigen-presenting cells activation” is not a canonical molecular target: the protein itself is pp65; “antigen-presenting cells activation” describes an immune process rather than a molecule. Caveat: - is_incorrect=true because the provided target name in the query “Cytomegalovirus phosphoprotein 65 antigen-presenting cells activation” conflates the molecule with an immunological process (antigen-presenting cell activation) rather than denoting a single protein or receptor. The scientifically accurate target is human cytomegalovirus lower matrix phosphoprotein 65 (pp65, UL83).
For immune therapies targeting this protein: - Stimulation of cytotoxic T lymphocyte response against cells expressing pp65 - Vaccine candidates may use pp65 or its peptides to induce protective immunity
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