Extended Data Fig. 8: Cardiotoxicity, inflammation and immune assessments after FAP CAR T cell transfer. | Nature

Extended Data Fig. 8: Cardiotoxicity, inflammation and immune assessments after FAP CAR T cell transfer.

From: Targeting cardiac fibrosis with engineered T cells

Extended Data Fig. 8: Cardiotoxicity, inflammation and immune assessments after FAP CAR T cell transfer.The alternative text for this image may have been generated using AI.

a, Volcano plot showing the differential expression of genes known to be modified in cardiotoxicity in the hearts of mice treated with either AngII/PE and FAP CAR T cells or a saline control for 4 weeks. Statistically significant changes are marked to indicate whether genes are expected to increase (orange) or decrease (blue) in the setting of cardiotoxicity. b, Differential expression of the same conditions in a at 8 weeks. a, b, Two-sided Welch’s t-test; n = 3 biologically independent mice per condition. c, Volcano plot showing the differential expression of 1,659 immune- and inflammation-related genes from hearts of mice treated with AngII/PE and FAP CAR T cells or AngII/PE for 4 weeks. In total, 22 genes were differentially expressed between the conditions. n = 3 mice per condition. d, Photomicrographs and quantification (mean ± s.e.m.) of immune cell (arrowheads) residency of the left ventricle at 4 weeks after either AngII/PE or AngII/PE and FAP CAR T cell treatment. Two-tailed unpaired Student’s t-test; n = 3 or 4 biologically independent mice, respectively. Scale bars, 100 μm.

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