hematopoietic system
• B cells exhibited defects in activation; proliferation was reduced in response to stimulators
|
• premature maturation of DN thymocytes which then undergo a high rate of apoptosis
|
• reduced proportion of DN3 T cells (CD4-, CD8-, CD25+, CD44lo)
• increased proportion of DN4 T cells (CD4-, CD8-, CD25-, CD44lo)
|
• CD5+, B220+ B cells absent in peritoneum, although B lymphocyte development in the bone marrow was normal
|
• reduced basal serum immunoglobulin levels, including IgM, IgG1, IgG2b, IgG3, and IgA
|
• impaired proliferative response of T cells in response to anti-CD3 antibody
|
immune system
• B cells exhibited defects in activation; proliferation was reduced in response to stimulators
|
• premature maturation of DN thymocytes which then undergo a high rate of apoptosis
|
• reduced proportion of DN3 T cells (CD4-, CD8-, CD25+, CD44lo)
• increased proportion of DN4 T cells (CD4-, CD8-, CD25-, CD44lo)
|
• CD5+, B220+ B cells absent in peritoneum, although B lymphocyte development in the bone marrow was normal
|
• reduced basal serum immunoglobulin levels, including IgM, IgG1, IgG2b, IgG3, and IgA
|
• impaired proliferative response of T cells in response to anti-CD3 antibody
|
cellular
• B cells exhibited defects in activation; proliferation was reduced in response to stimulators
|
• impaired proliferative response of T cells in response to anti-CD3 antibody
|