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γ干扰素和白细胞介素1可抑制轮状病毒进入人肠道细胞系,但α干扰素无此作用。

Interferon gamma and interleukin 1, but not interferon alfa, inhibit rotavirus entry into human intestinal cell lines.

作者信息

Bass D M

机构信息

Department of Pediatrics, and Stanford Center for Digestive Diseases, Stanford University, California 94305-5119, USA.

出版信息

Gastroenterology. 1997 Jul;113(1):81-9. doi: 10.1016/s0016-5085(97)70083-0.

Abstract

BACKGROUND & AIMS: Rotavirus, an important agent of gastroenteritis in children, causes diarrhea by infecting differentiated villus enterocytes in the small intestine. The aim of this study was to determine whether cytokines that can be expressed by mucosal cells have an effect on the rotavirus susceptibility of cultured human enterocytes.

METHODS

Caco-2 and HT-29 cells were pretreated with various cytokines before challenge with rotavirus.

RESULTS

Interleukin (IL)-1, interferon (IFN)-alpha, and IFN-gamma pretreatment led to a dose-dependent resistance to rotavirus infection. Maximum effects occurred after 72 hours of pretreatment, whereas no detectable inhibition occurred with <12 hours of pretreatment. Liposomal transfection of single-shelled and double-shelled rotavirus particles bypassed the block to rotavirus replication in IFN-gamma- and IL-1-treated but not IFN-alpha-treated cells. Binding studies with purified, metabolically labeled rotavirus showed no significant difference among IFN-gamma- and IFN-alpha-treated and control Caco-2 cells. Viral entry into Caco-2 cells was significantly inhibited by IFN-gamma and IL-1 but not IFN-alpha.

CONCLUSIONS

IFN-alpha and IFN-gamma induce rotavirus resistance by different mechanisms, suggesting that cytokines play a role in host defense against viral agents by changing the phenotype of intestinal epithelial cells.

摘要

背景与目的

轮状病毒是儿童肠胃炎的重要病原体,通过感染小肠中分化的绒毛肠上皮细胞引起腹泻。本研究的目的是确定黏膜细胞表达的细胞因子是否对培养的人肠上皮细胞的轮状病毒易感性有影响。

方法

在用轮状病毒攻击之前,用各种细胞因子预处理Caco-2和HT-29细胞。

结果

白细胞介素(IL)-1、干扰素(IFN)-α和IFN-γ预处理导致对轮状病毒感染的剂量依赖性抗性。预处理72小时后出现最大效应,而预处理<12小时则未检测到抑制作用。单壳和双壳轮状病毒颗粒的脂质体转染绕过了IFN-γ和IL-1处理但未用IFN-α处理的细胞中对轮状病毒复制的阻断。用纯化的、代谢标记的轮状病毒进行的结合研究表明,IFN-γ和IFN-α处理的Caco-2细胞与对照细胞之间没有显著差异。IFN-γ和IL-1可显著抑制病毒进入Caco-2细胞,但IFN-α则无此作用。

结论

IFN-α和IFN-γ通过不同机制诱导轮状病毒抗性,表明细胞因子通过改变肠上皮细胞表型在宿主抗病毒防御中发挥作用。

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