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干扰素(IFN)-α 的给药会加重 DBA/1J 小鼠的呼肠孤病毒 2 型引发的自身免疫性胰岛炎。

Administration of interferon (IFN)-α exacerbates reovirus type-2-triggered autoimmune insulitis in DBA/1J mice.

机构信息

Laboratory of Veterinary Pathology, The United Graduate School of Veterinary Science, Yamaguchi University, Yoshida, Yamaguchi, Japan.

出版信息

Scand J Immunol. 2012 Oct;76(4):378-86. doi: 10.1111/j.1365-3083.2012.02754.x.

Abstract

The aim of this study is to clarify the effects of administrated interferon (IFN)-α on Reovirus type-2 (Reo-2)-triggered autoimmune insulitis. Newborn DBA/1J mice infected with Reo-2 (on day 0) showed the highest titre in the pancreas on day 5 and thereafter the titre declined. Similar viral growth curve with lower titre was found in the spleen and thymus. Insulitis with impaired glucose tolerance developed in infected mice on day 10, but not on day 5. IFN-α was produced in the blood on days 3 and 5, but not on days 7 and 10. During the virus growth phase, IFN-α positive((+)) cells were detected in some pancreatic islet cells and infiltrated dendritic cells (DCs) in interstitium. Virus antigen positive cells were detected in islet cells, but not in DCs. Administration with IFN-α (10(2) , 10(3) or 10(4) international unit) on day 7, which is the time of the disappearance of virus from the pancreas and IFN-α from the blood, exacerbated insulitis with increased glucose values compared to only infected mice. IFN-α administration at the same time of infection did not develop insulitis. In addition, IFN-α administration in uninfected mice on day 7 did not cause any damage to islet cells. The present study suggests that IFN-α may have a possibility to exacerbate Reo-2-tiggered mild insulitis.

摘要

本研究旨在阐明干扰素(IFN)-α 对 2 型呼肠孤病毒(Reo-2)引发的自身免疫性胰岛炎的影响。新生 DBA/1J 小鼠在第 0 天感染 Reo-2 后第 5 天在胰腺中的滴度最高,此后滴度下降。在脾脏和胸腺中发现了相似的病毒生长曲线,但滴度较低。感染小鼠在第 10 天出现胰岛炎和糖耐量受损,但在第 5 天没有。IFN-α 在第 3 天和第 5 天在血液中产生,但在第 7 天和第 10 天没有。在病毒生长期间,在一些胰岛细胞和间质浸润的树突状细胞(DC)中检测到 IFN-α 阳性(+)细胞。在胰岛细胞中检测到病毒抗原阳性细胞,但在 DC 中没有。在第 7 天(即病毒从胰腺和血液中消失以及 IFN-α 消失的时间)给予 IFN-α(10(2)、10(3)或 10(4)国际单位)会导致胰岛炎加重,血糖值升高,与仅感染小鼠相比。在感染时给予 IFN-α 不会引起胰岛炎。此外,在第 7 天未感染的小鼠中给予 IFN-α 不会对胰岛细胞造成任何损害。本研究表明,IFN-α 可能有加重 Reo-2 触发的轻度胰岛炎的可能性。

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