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The Basis and Advances in Clinical Application of Cytomegalovirus-Specific Cytotoxic T Cell Immunotherapy for Glioblastoma Multiforme

Amin Daei SorkhabiImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, IranAila SarkeshImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, IranHossein SaeediImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, IranFaroogh MarofiDepartment of Hematology, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, IranMahnaz GhaebiCancer Gene Therapy Research Center (CGRC), Zanjan University of Medical Sciences, Zanjan, IranNicola SilvestrisMedical Oncology Unit, Department of Human Pathology "G. Barresi", University of Messina, Messina, ItalyBehzad BaradaranImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, IranOronzo BrunettiMedical Oncology Unit-Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Istituto Tumori "Giovanni Paolo II" of Bari, Bari, Italy
2022en
ABI

Аннотация

A high percentage of malignant gliomas are infected by human cytomegalovirus (HCMV), and the endogenous expression of HCMV genes and their products are found in these tumors. HCMV antigen expression and its implications in gliomagenesis have emerged as a promising target for adoptive cellular immunotherapy (ACT) strategies in glioblastoma multiforme (GB) patients. Since antigen-specific T cells in the tumor microenvironments lack efficient anti-tumor immune response due to the immunosuppressive nature of glioblastoma, CMV-specific ACT relies on in vitro expansion of CMV-specific CD8 + T cells employing immunodominant HCMV antigens. Given the fact that several hurdles remain to be conquered, recent clinical trials have outlined the feasibility of CMV-specific ACT prior to tumor recurrence with minimal adverse effects and a substantial improvement in median overall survival and progression-free survival. This review discusses the role of HCMV in gliomagenesis, disease prognosis, and recent breakthroughs in harnessing HCMV-induced immunogenicity in the GB tumor microenvironment to develop effective CMV-specific ACT.

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