Regulation of autoimmune diabetes by interleukin 3-dependent bone marrow-derived cells in NOD mice.

Regulation of autoimmune diabetes by interleukin 3-dependent bone marrow-derived cells in NOD mice.
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NOD 小鼠中白细胞介素 3 依赖性骨髓衍生细胞对自身免疫糖尿病的调节。

DOI:
10.1006/jaut.1997.0142
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发表时间:
1997
期刊:
Journal of autoimmunity.
影响因子:
--
通讯作者:
Maki,T
Maki,T
中科院分区:
--
文献类型:
--
作者:
Ito,A;Aoyanagi,N;Maki,T

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Interleukin-3 (IL-3), a multilineage colony stimulating factor, has been shown to augment alloreactive bone marrow-derived suppressor cell activity in vivo and in vitro. The present study examined the effect of IL-3 on autoimmune-mediated diabetes in NOD mice. Administration of IL-3 twice weekly starting at 2–4 weeks of age delayed the onset and reduced the overall incidence of diabetes. Bone marrow cells obtained from IL-3-treated NOD mice protected NOD mice from cyclophosphamide-induced diabetes but failed to prevent adoptively transferred diabetes. In vitro culture of bone marrow cells in medium containing IL-3 produced a Thy-1+CD3ϵloCD4−CD8−CD25−immature T cell clone which prevented cyclophosphamide-induced diabetes. The cloned cells also effectively delayed the development of diabetes induced by transfer of T cells in adult thymectomized, irradiated, bone marrow-reconstituted NOD mice. These results suggest that IL-3 is capable of regulating extrathymic T cell development from the bone marrow and that these cells mediate strong immunoregulatory function.
肥大细胞生长因子和 IL-3 支持骨髓驻留 T 细胞前体的体外生长。
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发表时间: 1992
影响因子: 4.4
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发表时间: 1992-04-15
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DOI: --
发表时间: 1981
影响因子: 158.5
作者:
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