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Virus-infected cell antigens refer to a broad group of antigens that are expressed on the surface or inside of cells following viral infection. These antigens typically consist of either viral proteins produced during the replication cycle within the host cell, or host cell proteins modified as a result of the infection. They are not a single molecular entity but a functional description encompassing the many possible peptides and proteins that the immune system can recognize as evidence of viral infection[3][4][5]. In adaptive immunity, these antigens are processed by infected cells and displayed on **major histocompatibility complex (MHC) class I molecules**, which are then recognized by cytotoxic T cells (CD8+), leading to targeted destruction of the infected cells and viral clearance[2][3][6]. Antibody-secreting B cells and helper T cells (CD4+) also participate in recognizing these antigens following antigen presentation by dendritic cells and macrophages on MHC class II molecules[4]. The phrase "virus-infected cell antigens" is not a standard molecular target or a unique protein, and is therefore *not* considered a canonical therapeutic target like a receptor, enzyme, or defined protein. Rather, it represents a category that is context-dependent and includes numerous possible antigens, making it too broad and non-specific for structured molecular target databases[3][4].
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