High plasma CXCL10 levels are associated with HCV-genotype 1, and higher insulin resistance, fibrosis, and HIV viral load in HIV/HCV coinfected patients

被引:21
作者
Berenguer, Juan [2 ]
Fernandez-Rodriguez, Amanda [1 ]
Angeles Jimenez-Sousa, Maria [1 ]
Cosin, Jaime [2 ]
Zarate, Paola [1 ,3 ]
Micheloud, Dariela [1 ,4 ]
Carlos Lopez, Juan [2 ]
Miralles, Pilar [2 ]
Catalan, Pilar [5 ]
Resino, Salvador [1 ,3 ]
机构
[1] Inst Salud Carlos III, Ctr Nacl Microbiol, Lab Mol Epidemiol Infect Dis, Madrid 28220, Spain
[2] Hosp Gen Gregorio Maranon, Infect Dis HIV Unit, Madrid, Spain
[3] Hosp Gen Gregorio Maranon, Family & Community Med Dept, Madrid, Spain
[4] Hosp Gen Gregorio Maranon, Dept Internal Med, Madrid, Spain
[5] Hosp Gen Gregorio Maranon, Dept Microbiol, Madrid, Spain
关键词
Chemokine; HOMA; AIDS; Chronic hepatitis C; Inflammation; HEPATITIS-C-VIRUS; GAMMA-INDUCIBLE PROTEIN-10; ACTIVE ANTIRETROVIRAL THERAPY; VIROLOGICAL RESPONSE; INFECTED PATIENTS; PLUS RIBAVIRIN; INTERFERON; EXPRESSION; IDENTIFICATION; INFLAMMATION;
D O I
10.1016/j.cyto.2011.10.020
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: CXCL10 may contribute to the host immune response against the hepatitis C virus (HCV), liver disease progression, and response to HCV antiviral therapy. The aim of our study was to analyze the relationship among virological, immunological, and clinical characteristics with plasma CXCL10 levels in human immunodeficiency virus (HIV)/HCV-coinfected patients. Methods: We carried out a cross-sectional study on 144 patients. CXCL10 and insulin were measured using an immunoassay kit. The degree of insulin resistance was estimated for each patient using the homeostatic model assessment (HOMA) method. Insulin resistance was defined as a HOMA index higher than or equal to 3.8. Aspartate aminotransferase (AST) to platelet ratio (APRI), FIB-4, Forns index, HGM1, and HGM2 were calculated. Results: The variables associated with log(10) CXCL10 levels by univariate analysis were age (b = 0.013; p = 0.023), prior AIDS-defining condition (6 = 0.127; p = 0.045), detectable plasma HIV viral load (b = 0.092; p = 0.006), log(10) HOMA (b = 0.216; p = 0.002), HCV-genotype 1 (b = 0.114; p = 0.071), and liver fibrosis assessed by all non-invasive indexes (log(10) APRI (b = 0.296; p = 0.001), log(10) FIB-4 (b = 0.436; p < 0.001), log(10) Forns index (b = 0.591; p < 0.001). log(10) HGM1 (b = 0.351; p = 0.021), and log(10) HGM2 (b = 0.215; p = 0.018)). However, in multivariate analysis, CXCL10 levels were only associated with HOMA, detectable plasma HIV viral load, HCV-genotype 1 and FIB-4 (R-square = 0.235; p < 0.001). Conclusion: Plasma CXCL10 levels were influenced by several characteristics of patients related to HIV and HCV infections, insulin resistance, and liver fibrosis, indicating that CXCL10 may play an important role in the pathogenesis of both HCV and HIV infections. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:25 / 29
页数:5
相关论文
共 30 条
[1]   Systemic and Intrahepatic Interferon-Gamma-Inducible Protein 10 kDa Predicts the First-Phase Decline in Hepatitis C Virus RNA and Overall Viral Response to Therapy in Chronic Hepatitis C [J].
Askarieh, Galia ;
Alsio, Asa ;
Pugnale, Paolo ;
Negro, Francesco ;
Ferrari, Carlo ;
Neumann, Avidan U. ;
Pawlotsky, Jean-Michel ;
Schalm, Solko W. ;
Zeuzem, Stefan ;
Norkrans, Gunnar ;
Westin, Johan ;
Soderholm, Jonas ;
Hellstrand, Kristoffer ;
Lagging, Martin .
HEPATOLOGY, 2010, 51 (05) :1523-1530
[2]   Identification of liver fibrosis in HIV/HCV-coinfected patients using a simple predictive model based on routine laboratory data [J].
Berenguer, J. ;
Bellon, J. M. ;
Miralles, P. ;
Alvarez, E. ;
Sanchez-Conde, M. ;
Cosin, J. ;
Lopez, J. C. ;
Alvarez, F. ;
CatalaN, P. ;
Resino, S. .
JOURNAL OF VIRAL HEPATITIS, 2007, 14 (12) :859-869
[3]   DNA oxidative damage in leukocytes correlates with the severity of HCV-related liver disease: validation in an open population study [J].
Cardin, R ;
Saccoccio, G ;
Masutti, F ;
Bellentani, S ;
Farinati, F ;
Tiribelli, C .
JOURNAL OF HEPATOLOGY, 2001, 34 (04) :587-592
[4]   Evidence for an antagonist form of the chemokine CXCL10 in patients chronically infected with HCV [J].
Casrouge, Armanda ;
Decalf, Jeremie ;
Ahloulay, Mina ;
Lababidi, Cyril ;
Mansour, Hala ;
Vallet-Pichard, Anais ;
Mallet, Vincent ;
Mottez, Estelle ;
Mapes, James ;
Fontanet, Arnaud ;
Pol, Stanislas ;
Albert, Matthew L. .
JOURNAL OF CLINICAL INVESTIGATION, 2011, 121 (01) :308-317
[5]   Chemokine antagonism in chronic hepatitis C virus infection [J].
Charles, Edgar D. ;
Dustin, Lynn B. .
JOURNAL OF CLINICAL INVESTIGATION, 2011, 121 (01) :25-27
[6]   Association of pretreatment serum interferon γ inducible protein 10 levels with sustained virological response to peginterferon plus ribavirin therapy in genotype 1 infected patients with chronic hepatitis C [J].
Diago, M ;
Castellano, G ;
García-Samaniego, J ;
Pérez, C ;
Fernández, I ;
Romero, M ;
Iacono, OL ;
García-Monzón, C .
GUT, 2006, 55 (03) :374-379
[7]   Identification of chronic hepatitis C patients without hepatic fibrosis by a simple predictive model [J].
Forns, X ;
Ampurdanès, S ;
Llovet, JM ;
Aponte, J ;
Quintó, L ;
Martínez-Bauer, E ;
Bruguera, M ;
Sánchez-Tapias, JM ;
Rodés, J .
HEPATOLOGY, 2002, 36 (04) :986-992
[8]   Innate immunity and chronic immune activation in HCV/HIV-1 co-infection [J].
Gonzalez, Veronica D. ;
Landay, Alan L. ;
Sandberg, Johan K. .
CLINICAL IMMUNOLOGY, 2010, 135 (01) :12-25
[9]   Expression of the chemokine IP-10 (CXCL10) by hepatocytes in chronic hepatitis C virus infection correlates with histological severity and lobular inflammation [J].
Harvey, CE ;
Post, JJ ;
Palladinetti, P ;
Freeman, AJ ;
Ffrench, RA ;
Kumar, RK ;
Marinos, G ;
Lloyd, AR .
JOURNAL OF LEUKOCYTE BIOLOGY, 2003, 74 (03) :360-369
[10]   Chemokines in the Immunopathogenesis of Hepatitis C Infection [J].
Heydtmann, Mathis ;
Adams, David H. .
HEPATOLOGY, 2009, 49 (02) :676-688