Abstract: |
Chimeric antigen receptor (CAR) T-cell therapy has resulted cytotoxicity mediated by the CAR and antigen-independent in remarkable clinical success in the treatment of B-cell ma- killing mediated through the interaction of LIGHT with lignancies. However, its clinical efficacy in solid tumors is lymphotoxin-β receptor on cancer cells. Moreover, CAR T cells limited, primarily by target antigen heterogeneity. To overcome expressing LIGHT had immunostimulatory properties that antigen heterogeneity, we developed CAR T cells that over- improved the cells’ proliferation and cytolytic profile. These express LIGHT, a ligand of both lymphotoxin-β receptor on data indicate that LIGHT-expressing CAR T cells may provide a cancer cells and herpes virus entry mediator on immune cells. way to eliminate antigen-negative tumor cells to prevent LIGHT-expressing CAR T cells displayed both antigen-directed antigen-negative disease relapse. ► ©2024 American Association for Cancer Research. |
Keywords: |
genetics; neoplasm; neoplasms; t lymphocyte; t-lymphocytes; mouse; animal; metabolism; animals; mice; drug screening; xenograft model antitumor assays; cell line, tumor; tumor antigen; immunology; antigens, neoplasm; tumor cell line; chimeric antigen receptor; cytotoxicity, immunologic; therapy; adoptive immunotherapy; immunotherapy, adoptive; procedures; immunocytotoxicity; lymphotoxin beta receptor; humans; human; tumor necrosis factor ligand superfamily member 14; receptors, chimeric antigen; herpesvirus entry mediator ligand
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