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. 2024 May 20;12(5):e009013. doi: 10.1136/jitc-2024-009013

Figure 4.

Figure 4

Membrane-proximal CD33-targeting chimeric antigen receptor (CAR) T cells provide enhanced survival in xenograft mouse model. (A) Schematic diagram of in vivo experimental setup. NCG mice were inoculated with U937-CD33high tumor and subsequently treated with CAR T cells. (B) Survival of NCG mice bearing U937-CD33high tumors and treated with titrated doses of CAR T cells (n=5; **p<0.01, *p<0.05). P values for survival determined by log-rank Mantel-Cox test, with 95% CI. (C) Tumor regression of NCG mice inoculated with U937-CD33high tumor and subsequently treated with 5.0×105 of CAR T cells. (D) Bioluminescence over time of U937-CD33high in tumor-bearing NCG mice treated with 5.0×105 CAR T cells. (E) Schematic diagram of in vivo experimental setup. NCG mice were inoculated with OCiAML3-CD33low tumor and subsequently treated with CAR T cells. (F) Survival of NCG mice inoculated with OCiAML3-CD33low tumors and treated with 5.0×105 CAR T cells (n=5; *p<0.05). P values for survival determined by log-rank Mantel-Cox test, with 95% CI. (G) Tumor regression of NCG mice bearing OCiAML3-CD33low tumors and treated with 5.0×105 CAR T cells. (H) Bioluminescence over time of OCiAML3-CD33low in tumor-bearing NCG mice treated with 5.0×105 CAR T cells.