<p>4–6 wk old NOD mice were transfused with CD4<sup>+</sup>CD25<sup>+</sup> T cells (either 1×10<sup>6</sup> (a) or 3×10<sup>6</sup> (b) per mouse) expanded by p509, p524 or p530. Untreated littermates were used as controls. In some cases, NOD recipients receiving 3×10<sup>6</sup> p524-expanded CD4<sup>+</sup>CD25<sup>+</sup> T cells were injected with neutralizing antibodies to IL-10/TGF-β according to the regimens described in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0007034#s2" target="_blank">Materials and Methods</a>. Development of diabetes was monitored for over 25 wks and the cumulative incidence of diabetes was shown from two experiments. The difference between untreated controls and mice treated with 1...
Beginning at the time of insulitis (7 wk of age), CD4+ and CD8+ mature thymocytes from nonobese diab...
<p>NOD mice received IDO-expressing fibroblasts upon initiation of spontaneous diabetes. At the endp...
Diabetes susceptibility in non-obese diabetic (NOD) mice may entail faulty activation of immunoregul...
<p>Diabetic splenocytes (1×10<sup>7</sup>) were co-transferred with or without CD4<sup>+</sup>CD25<s...
In the nonobese diabetic (NOD) mouse model of type 1 diabetes, the immune system recognizes many aut...
Most treatments that prevent autoimmune diabetes in nonobese diabetic (NOD) mice require interventio...
A deficit in IL-4 production has been previously reported in both diabetic human patients and non-ob...
OBJECTIVE: Blocking T-cell signaling is an effective means to prevent autoimmunity and allograft rej...
Non-obese diabetic (NOD) mice were injected with a rat monoclonal antibody to CD4 from birth every t...
BACKGROUND: We and others have previously demonstrated that treatment with bone marrow derived DC ge...
We and others have previously demonstrated that treatment with bone marrow derived DC genetically mo...
<p>NOD/scid recipient mice were transferred with either NOD mouse splenocytes (Nspl)(1×10<sup>7</sup...
The development of autoimmune diabetes in the nonobese diabetic (NOD) mouse results from a breakdown...
We have previously shown that nonobese diabetic (NOD) mice are selectively deficient in α/β-T cell r...
Diabetogenic T-cells can be detected in pre-diabetic nonobese diabetic (NOD) mice after transfer in ...
Beginning at the time of insulitis (7 wk of age), CD4+ and CD8+ mature thymocytes from nonobese diab...
<p>NOD mice received IDO-expressing fibroblasts upon initiation of spontaneous diabetes. At the endp...
Diabetes susceptibility in non-obese diabetic (NOD) mice may entail faulty activation of immunoregul...
<p>Diabetic splenocytes (1×10<sup>7</sup>) were co-transferred with or without CD4<sup>+</sup>CD25<s...
In the nonobese diabetic (NOD) mouse model of type 1 diabetes, the immune system recognizes many aut...
Most treatments that prevent autoimmune diabetes in nonobese diabetic (NOD) mice require interventio...
A deficit in IL-4 production has been previously reported in both diabetic human patients and non-ob...
OBJECTIVE: Blocking T-cell signaling is an effective means to prevent autoimmunity and allograft rej...
Non-obese diabetic (NOD) mice were injected with a rat monoclonal antibody to CD4 from birth every t...
BACKGROUND: We and others have previously demonstrated that treatment with bone marrow derived DC ge...
We and others have previously demonstrated that treatment with bone marrow derived DC genetically mo...
<p>NOD/scid recipient mice were transferred with either NOD mouse splenocytes (Nspl)(1×10<sup>7</sup...
The development of autoimmune diabetes in the nonobese diabetic (NOD) mouse results from a breakdown...
We have previously shown that nonobese diabetic (NOD) mice are selectively deficient in α/β-T cell r...
Diabetogenic T-cells can be detected in pre-diabetic nonobese diabetic (NOD) mice after transfer in ...
Beginning at the time of insulitis (7 wk of age), CD4+ and CD8+ mature thymocytes from nonobese diab...
<p>NOD mice received IDO-expressing fibroblasts upon initiation of spontaneous diabetes. At the endp...
Diabetes susceptibility in non-obese diabetic (NOD) mice may entail faulty activation of immunoregul...