immune system
N |
• no defects in T cell development in the thymus, spleen, or lymph nodes are dectected
• no alteration in cell viability, expression of cell surface activation markers, cell cycle progression, or cell size
|
• moderate suppression of overall proliferation after activation in vitro
|
• enhanced anti-inflammatory induced T regulatory cell differentiation in vitro
|
• inhibition in vitro
• however, there is no significant change in Th2 cell differentiation in vitro
|
• inhibition of differentiation in vitro
• treatment with NV118 (cell permeable succinate analogue) partially restores differentiation
|
• enhanced anti-inflammatory induced T regulatory cell differentiation in vitro
|
• significant protection from EAE pathogenic progression with more infiltrated FoxP3+CD4+ T cells and fewer infiltrated inflammatory CD4+T cells
|
cellular
• moderate suppression of overall proliferation after activation in vitro
|
hematopoietic system
• moderate suppression of overall proliferation after activation in vitro
|
• enhanced anti-inflammatory induced T regulatory cell differentiation in vitro
|
• inhibition in vitro
• however, there is no significant change in Th2 cell differentiation in vitro
|
• inhibition of differentiation in vitro
• treatment with NV118 (cell permeable succinate analogue) partially restores differentiation
|
• enhanced anti-inflammatory induced T regulatory cell differentiation in vitro
|