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CMV pp65 TCR-modified T cells is an adoptive cell therapy consisting of T cells genetically engineered, typically via lentiviral transduction, to express a T-cell receptor (TCR) specific for the cytomegalovirus (CMV) pp65 antigen (also known as UL83). This therapy is designed to recognize and eliminate CMV-infected cells by targeting pp65 epitopes presented by HLA class I molecules. It is primarily investigated for the treatment or prevention of CMV infection and reactivation in immunocompromised patients, such as those undergoing allogeneic hematopoietic stem cell transplantation (HSCT), where natural CMV-specific T-cell immunity is often deficient. The therapy targets multiple pp65 epitopes across major HLA-A alleles, enabling the engineered T cells to recognize and kill CMV-infected cells.
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