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第二届小鼠自身抗体研讨会:用于鉴定非肥胖糖尿病小鼠中胰岛素自身抗体的放射结合测定法在不同实验室间具有显著的一致性。

The second murine autoantibody workshop: remarkable interlaboratory concordance for radiobinding assays to identify insulin autoantibodies in nonobese diabetic mice.

作者信息

Yu Liping, Eisenbarth George, Bonifacio Ezio, Thomas James, Atkinson Mark, Wasserfall Clive

机构信息

Barbara Davis Center for Childhood Diabetes, University of Colorado Health Sciences Center, Denver, Colorado, USA.

出版信息

Ann N Y Acad Sci. 2003 Nov;1005:1-12. doi: 10.1196/annals.1288.002.

Abstract

In October 2000, the First Murine Autoantibody Workshop was held as part of an International Workshop on Lessons from Animal Models for Human Type 1 Diabetes. This first workshop identified insulin, but not glutamic acid decarboxylase (GAD) or IA-2, as specific autoantigens of humoral immunity in nonobese diabetic (NOD) mice. The goals of the Second Murine Autoantibody Workshop, part of the Sixth Annual Meeting of the IDS, were to increase the number of participating investigators, attempt standardization of insulin autoantibody (IAA) results across laboratories, identify serologic evidence of humoral immunity to other beta cell antigens, and allow for validation of ELISA assays for autoantibody detection in NOD mice. Sixty-three coded samples (26 pooled NOD sera, 23 pooled C57BL/6 sera, and 14 diluted samples of an anti-insulin monoclonal antibody) were distributed to 12 participating laboratories. This second workshop demonstrated that, for nearly all laboratories, IAA measured by radioimmunoassay (RIA) provided a sensitive and specific assay capable of distinguishing diabetes-prone from nondiabetes-prone mice. Analyses involving the serially diluted anti-insulin monoclonal antibody offered hope that a standard reference unit for reactivity could be established. Surprisingly, two ELISA assays for IAA detection proved remarkably sensitive (i.e., 65% and 92%). However, subsequent absorption studies performed after the workshop (presented at the IDS meeting) brought into question whether ELISA assays for IAA do, in reality, detect anti-insulin immunities and whether assays for GAD and IA-2 autoantibodies distinguish diabetes-prone from nondiabetes-prone mice. In sum, this workshop continued to support the notion that IAA, as determined by RIA, could provide a sensitive and specific marker of anti-beta cell immunity in NOD mice.

摘要

2000年10月,作为“人类1型糖尿病动物模型经验国际研讨会”的一部分,第一届小鼠自身抗体研讨会召开。第一届研讨会确定胰岛素为非肥胖糖尿病(NOD)小鼠体液免疫的特异性自身抗原,但未将谷氨酸脱羧酶(GAD)或IA-2确定为特异性自身抗原。作为国际糖尿病学会第六届年会一部分的第二届小鼠自身抗体研讨会的目标是增加参与研究的人员数量,尝试使各实验室间胰岛素自身抗体(IAA)检测结果标准化,确定针对其他β细胞抗原的体液免疫的血清学证据,并验证用于检测NOD小鼠自身抗体的ELISA检测方法。63个编码样本(26份混合的NOD血清、23份混合的C57BL/6血清以及14份抗胰岛素单克隆抗体的稀释样本)被分发给12个参与实验室。第二届研讨会表明,对于几乎所有实验室而言,通过放射免疫测定法(RIA)检测的IAA提供了一种灵敏且特异的检测方法,能够区分易患糖尿病的小鼠和不易患糖尿病的小鼠。涉及系列稀释抗胰岛素单克隆抗体的分析带来了建立反应性标准参考单位的希望。令人惊讶的是,两种用于检测IAA的ELISA检测方法被证明具有极高的灵敏度(即分别为65%和92%)。然而,研讨会之后进行的后续吸收研究(在国际糖尿病学会会议上展示)引发了质疑,即IAA的ELISA检测方法在实际中是否真的能检测到抗胰岛素免疫,以及GAD和IA-2自身抗体检测方法能否区分易患糖尿病的小鼠和不易患糖尿病的小鼠。总之,本次研讨会继续支持这样一种观点,即通过RIA测定的IAA可作为NOD小鼠抗β细胞免疫的灵敏且特异的标志物。

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