Figure 7.
Oral administration with VEN-120 attenuates chronic murine ileitis. A, B] H&E staining demonstrates improved architectural appearance and decreased chronic and acute inflammation following oral administration of VEN-120 or subcutaneous anti-TNF antibody, infliximab [IFX] [*p < 0.05; ***p < 0.0001, Student’s t test]. Flow cytometric analysis demonstrating that VEN-120 administration significantly decreases CD4+ burden at C] the LP, and D] at the MLN in TNFΔARE/+ mice. Further interrogation of these T cells identified a significant increase in IL-10 at the E] LP but not the F] MLN of TNFΔARE/+ mice treated with VEN-120. A significant reduction in IL-17 expressing cells was demonstrated at G] the LP but not H] the MLN of TNFΔARE/+ mice treated with VEN-120 [*p < 0.05; **p < 0.01, one-way ANOVA, n = 6]. MLN, mesenteric lymph nodes; LP, lamina propria; ANOVA, analysis of variance; H&E, haematoxylin and eosin; TNF, tumour necrosis factor.

Oral administration with VEN-120 attenuates chronic murine ileitis. A, B] H&E staining demonstrates improved architectural appearance and decreased chronic and acute inflammation following oral administration of VEN-120 or subcutaneous anti-TNF antibody, infliximab [IFX] [*p < 0.05; ***p < 0.0001, Student’s t test]. Flow cytometric analysis demonstrating that VEN-120 administration significantly decreases CD4+ burden at C] the LP, and D] at the MLN in TNFΔARE/+ mice. Further interrogation of these T cells identified a significant increase in IL-10 at the E] LP but not the F] MLN of TNFΔARE/+ mice treated with VEN-120. A significant reduction in IL-17 expressing cells was demonstrated at G] the LP but not H] the MLN of TNFΔARE/+ mice treated with VEN-120 [*p < 0.05; **p < 0.01, one-way ANOVA, n = 6]. MLN, mesenteric lymph nodes; LP, lamina propria; ANOVA, analysis of variance; H&E, haematoxylin and eosin; TNF, tumour necrosis factor.

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