immune system
• the percentage of mature (CD69loCD62Lhi) single-positive thymocytes is decreased in these mice
|
• CD4+ T cell numbers in the periphery are significantly decreased about 5-fold
|
• CD8+ T cell numbers in the periphery are significantly decreased about 5-fold
|
• in vitro transwell assays demonstrate migration defects in thymic CD4+ T cells' response to sphingosine 1-phosphate, CCL21, and CXCL12
• similar defects are observed in the migratory response of CD4+CD8+ T cells to CXCL12 and of splenic CD4+ T cells to CCL21
|
hematopoietic system
• the percentage of mature (CD69loCD62Lhi) single-positive thymocytes is decreased in these mice
|
• CD4+ T cell numbers in the periphery are significantly decreased about 5-fold
|
• CD8+ T cell numbers in the periphery are significantly decreased about 5-fold
|
• in vitro transwell assays demonstrate migration defects in thymic CD4+ T cells' response to sphingosine 1-phosphate, CCL21, and CXCL12
• similar defects are observed in the migratory response of CD4+CD8+ T cells to CXCL12 and of splenic CD4+ T cells to CCL21
|
endocrine/exocrine glands
• the percentage of mature (CD69loCD62Lhi) single-positive thymocytes is decreased in these mice
|
Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive | DOID:0090014 |
OMIM:608971 |
J:141431 |