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- Ba4f34fa58c33eca74d88e5a49e7d966a NCIT_P378 "NCI" @default.
- Ba4f34fa58c33eca74d88e5a49e7d966a type Axiom @default.
- Ba4f34fa58c33eca74d88e5a49e7d966a annotatedProperty IAO_0000115 @default.
- Ba4f34fa58c33eca74d88e5a49e7d966a annotatedSource NCIT_C180570 @default.
- Ba4f34fa58c33eca74d88e5a49e7d966a annotatedTarget "A preparation of T-lymphocytes that have been genetically modified to express a chimeric antigen receptor (CAR) targeting the tumor-associated antigen (TAA) CD19 and containing a short hairpin RNA (shRNA) against the pro-inflammatory cytokine interleukin-6 (IL-6), and linked to the intracellular signaling domains of 4-1BB (CD137) and the zeta chain of the TCR/CD3 complex (TCRzeta; CD247; CD3zeta), with potential immunostimulating and antineoplastic activities. Upon administration, short hairpin RNA-IL-6 gene silencing anti-CD19 CAR T cells target and bind to CD19-expressing tumor cells, thereby inducing selective toxicity in CD19-expressing tumor cells. CD19 antigen is a B-cell specific cell surface antigen expressed in all B-cell lineage malignancies. IL-6 gene silencing reduces IL-6 gene expression and release. This may inhibit IL-6-mediated toxicity due to high IL-6 levels and may prevent severe cytokine release syndrome (CRS) and CAR-T-related encephalopathy (CRES)." @default.