mortality/aging
• in mice infected with Mycobacteria tuberculosis H37Rv or Citrobacter rodentium compared with C57BL/6J wild-type mice
|
• following infection with Plasmodium berghei ANKA-parasitized red blood cells to induce cerebral malaria, mice exhibit longer survival compared with C57BL/6J wild-type mice
• however, splenocytes from infected C57BL/10J restores susceptibility
|
immune system
small thymus
(
J:185217
)
• in mice infected with Mycobacterium bovis BCG
|
• in the spleen
|
• complete absence of CD19+ B cells in the bone marrow
|
• in the spleen
|
• in the thymus
|
• severe in the thymus and spleen
|
• from total spleen cells in response to activation along the Th1 pathway
|
• mice infected with Mycobacterium bovis BCG exhibit splenomegaly and increased spleen bacterial count compared with C57BL/6J wild-type mice
|
• in mice infected with Mycobacteria tuberculosis H37Rv or Citrobacter rodentium compared with C57BL/6J wild-type mice
|
• following infection with Plasmodium berghei ANKA-parasitized red blood cells to induce cerebral malaria, mice exhibit longer survival compared with C57BL/6J wild-type mice
• however, splenocytes from infected C57BL/10J restores susceptibility
|
hematopoietic system
small thymus
(
J:185217
)
• in mice infected with Mycobacterium bovis BCG
|
• in the spleen
|
• complete absence of CD19+ B cells in the bone marrow
|
• in the spleen
|
• in the thymus
|
• severe in the thymus and spleen
|
• in the bone marrow
|
endocrine/exocrine glands
small thymus
(
J:185217
)
growth/size/body
• in mice infected with Mycobacterium bovis BCG
|