Genes outside the MHC create a general susceptibility to autoimmunity in non-obese diabetic (NOD) mice. In this study, we describe marked differences in dendritic cell generation, in vitro, caused by non-MHC NOD genes. Bone marrow cells from NOD.H-2k mice cultured in vitro with GM-CSF and IL-4 generated a reduced yield of dendritic cells when compared to bone marrow cells from B10.H-2k mice. This was due to failure to pass through successive rounds of cell division and elevated levels of apoptosis in NOD.H-2k precursor cells. This aberrant response to GM-CSF and IL-4 was unique to the NOD.H-2k background when compared to bone marrow cells from other H-2k congenic strains, and coculture experiments showed that it was cell-autonomous. Overall...
The objective of the study was to identify immune cell populations, in addition to Foxp3+ T-regulato...
Autoreactive T cells clearly mediate the pancreatic beta cell destruction causing type 1 diabetes (T...
One mechanism whereby B cells contribute to type 1 diabetes in nonobese diabetic (NOD) mice is as a ...
Genes outside the MHC create a general susceptibility to autoimmunity in non-obese diabetic (NOD) mi...
The pathogenesis of diabetes in the nonobese diabetic (NOD) mouse is characterized by a selective de...
The NOD mouse spontaneously develops autoimmune diabetes. Dendritic cells (DC) play a crucial role i...
Aberrant dendritic cell (DC) development and function may contribute to autoimmune disease susceptib...
Although T lymphocytes are the ultimate effectors of pancreatic beta cell destruction in autoimmune ...
The nonobese diabetic (NOD) mouse is a spontaneous animal model for type 1 diabetes characterized by...
Genetically-controlled defects in the development and function of antigen presenting cells may expla...
Dendritic cells govern the outcome of an immune response toward either tolerance or autoimmunity. Re...
The development of autoimmune diabetes in the nonobese diabetic (NOD) mouse is controlled by multipl...
OBJECTIVE: Although the H2(g7) major histocompatibility complex (MHC) provides the primary pathogeni...
Abstract: NOD mice spontaneously develop diabe-tes between 15 and 20 weeks of age, which is preceded...
The objective of the study was to identify immune cell populations, in addition to Foxp3+ T-regulato...
The objective of the study was to identify immune cell populations, in addition to Foxp3+ T-regulato...
Autoreactive T cells clearly mediate the pancreatic beta cell destruction causing type 1 diabetes (T...
One mechanism whereby B cells contribute to type 1 diabetes in nonobese diabetic (NOD) mice is as a ...
Genes outside the MHC create a general susceptibility to autoimmunity in non-obese diabetic (NOD) mi...
The pathogenesis of diabetes in the nonobese diabetic (NOD) mouse is characterized by a selective de...
The NOD mouse spontaneously develops autoimmune diabetes. Dendritic cells (DC) play a crucial role i...
Aberrant dendritic cell (DC) development and function may contribute to autoimmune disease susceptib...
Although T lymphocytes are the ultimate effectors of pancreatic beta cell destruction in autoimmune ...
The nonobese diabetic (NOD) mouse is a spontaneous animal model for type 1 diabetes characterized by...
Genetically-controlled defects in the development and function of antigen presenting cells may expla...
Dendritic cells govern the outcome of an immune response toward either tolerance or autoimmunity. Re...
The development of autoimmune diabetes in the nonobese diabetic (NOD) mouse is controlled by multipl...
OBJECTIVE: Although the H2(g7) major histocompatibility complex (MHC) provides the primary pathogeni...
Abstract: NOD mice spontaneously develop diabe-tes between 15 and 20 weeks of age, which is preceded...
The objective of the study was to identify immune cell populations, in addition to Foxp3+ T-regulato...
The objective of the study was to identify immune cell populations, in addition to Foxp3+ T-regulato...
Autoreactive T cells clearly mediate the pancreatic beta cell destruction causing type 1 diabetes (T...
One mechanism whereby B cells contribute to type 1 diabetes in nonobese diabetic (NOD) mice is as a ...