Increased expression and dysregulated association of restriction factors and type I interferon in HIV, HCV mono- and co-infected patients

被引:12
作者
Zhu, Jia-Wu [1 ,2 ]
Liu, Feng-Liang [1 ]
Mu, Dan [1 ,2 ]
Deng, De-Yao [3 ]
Zheng, Yong-Tang [1 ,2 ]
机构
[1] Chinese Acad Sci, Chinese Acad Sci & Yunnan Prov, Kunming Inst Zool, Key Lab Anim Models & Human Dis Mech, Kunming 650223, Yunnan, Peoples R China
[2] Univ Chinese Acad Sci, Kunming Coll Life Sci, Kunming, Yunnan, Peoples R China
[3] Second Peoples Hosp Yunnan Prov, Dept Clin Lab, Kunming, Yunnan, Peoples R China
基金
中国国家自然科学基金;
关键词
HIV; HCV; co-infection; restriction factors; type I interferon; MESSENGER-RNA LEVELS; CHRONIC HEPATITIS-C; VIRUS-INFECTION; DISEASE PROGRESSION; APOBEC3G; GENE; TRIM5-ALPHA; COINFECTION; LIVER; REPLICATION;
D O I
10.1002/jmv.24419
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Host restriction factors and type I interferon are important in limiting HIV and HCV infections, yet the role of HIV, HCV mono- and co-infection in regulating these antiviral genes expression is not clear. In this study, we measured the levels of TRIM5, TRIM22, APOBEC3G, and IFN-, - mRNA expression in peripheral blood mononuclear cells of 43 HIV mono-infected, 70 HCV mono-infected and 64 HIV/HCV co-infected patients along with 98 healthy controls. We also quantified HIV and HCV viral loads in mono- and co-infected patients. The results showed that HCV, HIV mono- and co-infection differentially increased TRIM22, APOBEC3G, and IFN-, - mRNA expression while the mRNA expression of TRIM was upregulated only by HCV-mono infection. HIV/HCV co-infection was associated with higher viral load, compared to either HIV or HCV mono-infection. Additionally, we showed TRIM and TRIM22 positively correlated with IFN-, -, which could be dysregulated by HIV, HCV mono- and co-infection. Furthermore, we found TRIM22 negatively correlated with HCV viral load in mono-infected patients and APOBEC3G positively correlated with HCV viral load in co-infected patients. Collectively, our findings suggest the potential role of restriction factors in restricting HIV, HCV mono- and co-infection in vivo, which appears to be a therapeutic target for potential drug discovery. J. Med. Virol. 88:987-995, 2016. (c) 2015 Wiley Periodicals, Inc.
引用
收藏
页码:987 / 995
页数:9
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