Journal of Immunotherapy · 2004 · 27 citations · 41 references
Cytotoxic T LymphocytesEndothelial CellsImmunologyTumor Endothelial CellsCell DeathImmunologic MechanismEndoglin-positive Endothelial CellsImmunotherapyEndocytic PathwayCell SignalingAutoimmunityVascular BiologyTumor TargetingCell BiologyTumor MicroenvironmentScdb Edgcd3Endothelial DysfunctionImmune Checkpoint InhibitorMedicine
We present a novel vascular tumor therapy approach based on lysing endothelial cells by cytotoxic T lymphocytes (CTLs). Retargeting of CTLs is achieved by a recombinant bispecific antibody molecule (bispecific single-chain diabody) directed against human endoglin (CD105, EDG) and the T-cell coreceptor CD3 (scDb EDGCD3). Bacterially expressed scDb EDGCD3 was able to bind to endoglin-expressing endothelial cells as well as CD3-expressing T lymphocytes. The single-chain diabody mediated killing of endothelial cells (HUVEC, HMEC) by activated cytotoxic T lymphocytes at picomolar concentrations, and cells not expressing endoglin were not affected. Because endoglin is up-regulated in the vasculature of many solid tumors, this antibody molecule should be capable of lysing tumor endothelial cells and thus destroying the vascular bed of the tumor.
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Prostate-specific membrane antigen is produced in tumor-associated neovasculature.
Sam S. Chang, Denise S. O’Keefe, Dean J. Bacich et al. · PubMed · 1999 · 464 citations
Torsten Dreier, Grit Lorenczewski, Christian Brandl et al. · International Journal of Cancer · 2002 · 349 citations · Full text