Human immunodeficiency virus-related microbial translocation and progression of hepatitis C

被引:223
作者
Balagopal, Ashwin [1 ]
Philp, Frances H. [1 ]
Astemborski, Jacquie [1 ,2 ]
Block, Timothy M. [3 ,4 ]
Mehta, Anand [3 ,4 ]
Long, Ronald [3 ,4 ]
Kirk, Gregory D. [1 ,2 ]
Mehta, Shruti H. [1 ,2 ]
Cox, Andrea L. [1 ]
Thomas, David L. [1 ,2 ]
Ray, Stuart C. [1 ]
机构
[1] Johns Hopkins Med Inst, Dept Med, Div Infect Dis, Viral Hepatitis Ctr, Baltimore, MD 21205 USA
[2] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Epidemiol, Baltimore, MD USA
[3] Drexel Coll Med, Hepatitis B Fdn, Doylestown, PA USA
[4] Drexel Coll Med, Drexel Inst Biotechnol & Virol Res, Doylestown, PA USA
关键词
D O I
10.1053/j.gastro.2008.03.022
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background&Aims: Human immunodeficiency virus (HIV)-l infection has been associated with enhanced microbial translocation, and microbial translocation is a mechanism through which alcohol and some enteric conditions cause liver disease. We hypothesized that HIV promotes liver disease by enhancing microbial translocation. Methods: We studied human cohorts in which hepatitis C virus (HCV) and HIV outcomes were carefully characterized. Results: HIV-related CD4(+) lymphocyte depletion was strongly associated with microbial translocation as indicated by elevated levels of circulating hpopolysaccharide (LPS), LPS-binding protein, soluble CD14, and fucose-binding lectin (AAL) reactive to immunoglobulin G specific for the a-galactose epitope and suppressed levels of endotoxin core antibodies (EndoCAb IgM) in HIV-infected subjects compared with the same persons before they had HIV infection and compared with HIV-uninfected subjects. The same measures of microbial translocation were strongly associated with HCV-related liver disease progression (cirrhosis), eg, LPS, odds ratio, 19.0 (P =.002); AAL, odds ratio, 27.8 (P <.0001); in addition, levels of LPS were elevated prior to recognition of cirrhosis. Conclusions: Microbial translocation may be a fundamental mechanism through which HIV accelerates progression of chronic liver disease.
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页码:226 / 233
页数:8
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