mortality/aging
• compared with wild-type mice and Faslgld homozygotes
|
immune system
N |
• mice mount a normal immune response to influenza
|
• T cells are less efficient than wild-type cells at killing CH1 cells
|
• at 12 to 20 weeks
|
• 62% of terminally ill mice exhibit systemic lupus erythematosus-like (SLE) autoimmune disease with cellular crescents, protein casts, and compliment in renal glomeruli unlike wild-type mice
• mice develop more severe SLE-like disease than Faslgld homozygotes
• by 57 weeks, 50% of mice develop fatal SLE-like autoimmune kidney disease compared with 15% of Faslgld homozygotes
|
• higher than in wild-type mice and Faslgld homozygotes
|
• higher than in wild-type mice and Faslgld homozygotes
|
• mice develop SLE-like glomerulonephritis unlike wild-type mice and more frequently than Faslgld homozygotes
|
dermatitis
(
J:153501
)
• 30% of mice develop severe dermatitis with lesions on the ears and necks unlike wild-type mice
|
renal/urinary system
• mice develop SLE-like glomerulonephritis unlike wild-type mice and more frequently than Faslgld homozygotes
|
• 62% of terminally ill mice exhibit SLE-like glomerulonephritis with cellular crescents in the renal glomeruli
|
renal cast
(
J:153501
)
• 62% of terminally ill mice exhibit SLE-like glomerulonephritis with protein casts
|
neoplasm
• by 78 weeks, 27% of mice develop hepatic tumors with characteristics of histiocytic sarcoma with deposits in the spleen and lungs
|
• by 78 weeks, 27% of mice develop hepatic tumors with characteristics of histiocytic sarcoma with deposits in the spleen and lungs
|
homeostasis/metabolism
• at 12 to 20 weeks
|
hematopoietic system
• T cells are less efficient than wild-type cells at killing CH1 cells
|
integument
dermatitis
(
J:153501
)
• 30% of mice develop severe dermatitis with lesions on the ears and necks unlike wild-type mice
|
liver/biliary system
• by 78 weeks, 27% of mice develop hepatic tumors with characteristics of histiocytic sarcoma with deposits in the spleen and lungs
|
growth/size/body