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人类自身免疫性糖尿病中的CD4 + CD25高表达调节性T细胞

CD4+CD25high regulatory T cells in human autoimmune diabetes.

作者信息

Putnam Amy L, Vendrame Francesco, Dotta Francesco, Gottlieb Peter A

机构信息

Barbara Davis Center for Childhood Diabetes, University of Colorado Health Sciences Center, 4200 East Ninth Avenue, Box B140, Denver, CO, USA.

出版信息

J Autoimmun. 2005 Feb;24(1):55-62. doi: 10.1016/j.jaut.2004.11.004. Epub 2005 Jan 12.

Abstract

In mouse models, CD4+CD25+ T cells are involved in maintenance of peripheral tolerance. In humans, a subset of CD4+CD25+ T cells expressing high levels of CD25 (CD4+CD25high) with characteristics identical to murine CD4+CD25+ was recently described. We evaluated the characteristics of CD4+CD25high T cells in peripheral blood of type 1 diabetic subjects (T1D) and normal controls (NC). In contrast to a previous report, we found no difference in the number of CD4+CD25high and CD4+CD25+ T cells between T1D and NC. We confirmed previous studies that demonstrated that human CD4+CD25high cells can suppress the proliferation of co-cultured CD4+CD25- cells stimulated in conditions of sub-maximal cross-linking by anti-CD3 either with or without anti-CD28. However, we did not observe statistical differences between the normal controls and the chronic diabetic subjects we tested. Culturing of these cell populations did not appear to affect their ability to suppress proliferation in both groups. In conclusion, we found no significant differences in number or in vitro regulatory function of CD4+CD25high in chronic human T1D subjects.

摘要

在小鼠模型中,CD4+CD25+ T细胞参与维持外周耐受。在人类中,最近描述了一类表达高水平CD25的CD4+CD25+ T细胞亚群(CD4+CD25high),其特征与小鼠CD4+CD25+ T细胞相同。我们评估了1型糖尿病患者(T1D)和正常对照(NC)外周血中CD4+CD25high T细胞的特征。与之前的一份报告相反,我们发现T1D患者和NC之间CD4+CD25high和CD4+CD25+ T细胞的数量没有差异。我们证实了先前的研究,即人类CD4+CD25high细胞能够抑制在亚最大交联条件下由抗CD3单独或联合抗CD28刺激的共培养CD4+CD25-细胞的增殖。然而,我们在正常对照和我们测试的慢性糖尿病患者之间未观察到统计学差异。培养这些细胞群体似乎并未影响两组细胞抑制增殖的能力。总之,我们发现慢性人类T1D患者中CD4+CD25high细胞的数量或体外调节功能没有显著差异。

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