mortality/aging
• in vesicular stomatitis virus (VSV)-infected mice
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immune system
N |
• mice exhibit normal T cell dependent immune response
|
• when cells are used in adoptive transfer experiments in Rag1 null mice
|
• in uninduced and BCR-stimulated mice
|
• adoptive transfer experiments confirm that the defects in B cell homeostasis is B cell intrinsic
|
• recirculating B cells are decreased compared to in wild-type mice
• splenic B cells are decreased compared to in wild-type mice
|
• the splenic B cell zone is smaller, the T cell zone is not consistently surrounded by B cells, the follicular B cell area is smaller, and the marginal zone B cell area is absent compared to in wild-type mice
|
• decreased
|
• in vesicular stomatitis virus (VSV)-infected mice
|
• following TNP-Ficoll injection
|
• vesicular stomatitis virus (VSV)-infected mice exhibit decreased IgG levels and increased mortality compared with similarly treated wild-type mice
|
• in vesicular stomatitis virus (VSV)-infected mice
|
hematopoietic system
• when cells are used in adoptive transfer experiments in Rag1 null mice
|
• in uninduced and BCR-stimulated mice
|
• adoptive transfer experiments confirm that the defects in B cell homeostasis is B cell intrinsic
|
• recirculating B cells are decreased compared to in wild-type mice
• splenic B cells are decreased compared to in wild-type mice
|
• the splenic B cell zone is smaller, the T cell zone is not consistently surrounded by B cells, the follicular B cell area is smaller, and the marginal zone B cell area is absent compared to in wild-type mice
|
• decreased
|
• in vesicular stomatitis virus (VSV)-infected mice
|
• following TNP-Ficoll injection
|
cellular
• when cells are used in adoptive transfer experiments in Rag1 null mice
|
• in uninduced and BCR-stimulated mice
|