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Expansion of CD4+CD25+FoxP3+ Regulatory T Cells in Chronic Hepatitis C Virus Infection | ||
Iranian Journal of Immunology | ||
مقاله 5، دوره 7، شماره 3، آذر 2010، صفحه 177-185 اصل مقاله (1.8 M) | ||
نوع مقاله: Original Article | ||
نویسندگان | ||
Tyebeha Hashempoor1؛ Taravat Bamdad* 1، 2؛ Shahin Merat3؛ Ehsan Janzamin4؛ Leila Nemati4؛ Hossain Jabbari3؛ Amir-Houshang Sharifi3؛ Hediyeh Zamini3 | ||
1Department of Virology, School of Medical Sciences, Tarbiat Modares University of Medical Sciences | ||
2Research and Development Center for Biotechnology (RDCB), Tarbiat Modares University, Tehran, Iran | ||
3Digestive Disease Research Center, Shariati Hospital, Tehran University of Medical Sciences | ||
4Rooyan Institute | ||
چکیده | ||
Background: Regulatory T cells (Tregs) have been involved in impaired immunity and may have a pivotal role in persistence of viral infections. Objective: To develop a simple and reliable in-house three color flow cytometery of peripheral blood to understand the role of HCV infection in the increase of Tregs. Methods: The level of naturally occurring CD4+CD25+FoxP3+ regulatory T cells (nTregs) in 20 chronically infected with hepatitis C virus (HCV) patients was compared to those of 15 healthy individuals by flowcytometry. In a different approach we performed permeabilization and intracellular staining before surface staining which allows the preservation of the surface molecules in the combined detection process and results in the normal frequency of nTregs in blood. Results: Using the optimized method, it was shown that a significantly higher proportion of nTregs in the total CD4+ T cell population was seen in the peripheral blood of chronic HCV patients (0.83 ± 0.21%, p=0.05) as compared to controls (0.26 ± 0.1, p=0.05). Conclusions: In accordance with other studies, we showed that HCV infection induces a dramatic increase in Tregs, which might contribute to the immune response failure during HCV infection. | ||
کلیدواژهها | ||
Hepatitis C Virus؛ Flowcytometry Method؛ Natural Regulatory T Cells | ||
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