Figure 2
Figure 2. Absence of MIF delays CLL development and prolongs overall survival. (A) WBC (top panel) and malignant (IgM+CD5+) B cells (bottom panel) over time in TCL1+/wtMIFwt/wt (●) and TCL1+/wtMIF−/− (○) mice. Y-axis modified to accommodate high cell counts in leukemic mice. TCL1+/wtMIFwt/wt mice have higher WBC and malignant B cells than TCL1+/wtMIF−/− mice. (B) Incidence of CLL over time. TCL1+/wtMIFwt/wt mice develop leukemia with a WBC > 20 × 109/L more frequently than TCL1+/wtMIF−/− mice (P = .02, log rank test). Y-axis truncated at 50% because not all animals develop WBC > 20 × 109/L. (C) Increased spleen and liver weight in TCL1+/wtMIFwt/wt versus TCL1+/wtMIF−/− mice at month 12. (D) Prolonged overall survival of TCL1+/wtMIF−/− (n = 60) versus TCL1+/wtMIFwt/wt mice (n = 60). The difference of 80 days was significant with P = .0003 (log-rank test). + indicates censored events (not caused by CLL).

Absence of MIF delays CLL development and prolongs overall survival. (A) WBC (top panel) and malignant (IgM+CD5+) B cells (bottom panel) over time in TCL1+/wtMIFwt/wt (●) and TCL1+/wtMIF−/− (○) mice. Y-axis modified to accommodate high cell counts in leukemic mice. TCL1+/wtMIFwt/wt mice have higher WBC and malignant B cells than TCL1+/wtMIF−/− mice. (B) Incidence of CLL over time. TCL1+/wtMIFwt/wt mice develop leukemia with a WBC > 20 × 109/L more frequently than TCL1+/wtMIF−/− mice (P = .02, log rank test). Y-axis truncated at 50% because not all animals develop WBC > 20 × 109/L. (C) Increased spleen and liver weight in TCL1+/wtMIFwt/wt versus TCL1+/wtMIF−/− mice at month 12. (D) Prolonged overall survival of TCL1+/wtMIF−/− (n = 60) versus TCL1+/wtMIFwt/wt mice (n = 60). The difference of 80 days was significant with P = .0003 (log-rank test). + indicates censored events (not caused by CLL).

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