The response to TLR ligation of human CD16+CD14- monocytes is weakly modulated as a consequence of persistent infection with the hepatitis C virus

Molecular Immunology

Volumn 48, Issue 12-13, 2011, Pages 1505-1511

  Peng, Cheng ^a,b   Liu, Bi Sheng ^a   de Knegt, Robert J ^a   Janssen, Harry L A ^a   Boonstra, André ^a  

^a ERASMUS MEDICAL CENTER   (Netherlands)

^b HUAZHONG UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

Author keywords

Hepatitis C virus; Monocyte subset; TLR; Viral infection

Indexed keywords

ALANINE AMINOTRANSFERASE; CD14 ANTIGEN; CD16 ANTIGEN; MACROPHAGE INFLAMMATORY PROTEIN 1BETA; TOLL LIKE RECEPTOR;

ADULT; ALANINE AMINOTRANSFERASE BLOOD LEVEL; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; HEPATITIS C; HEPATITIS C VIRUS; HUMAN; HUMAN CELL; LIVER FIBROSIS; MALE; MONOCYTE; PERSISTENT VIRUS INFECTION; PRIORITY JOURNAL; VIRUS LOAD; VIRUS PATHOGENESIS;

ADULT; ANTIGENS, CD14; CELL COUNT; CHEMOKINE CCL4; CYTOKINES; FEMALE; HEPACIVIRUS; HEPATITIS C, CHRONIC; HUMANS; IMIDAZOLES; LIPOPOLYSACCHARIDES; MALE; MIDDLE AGED; MONOCYTES; RECEPTORS, IGG; TOLL-LIKE RECEPTOR 4; TOLL-LIKE RECEPTOR 8; TUMOR NECROSIS FACTOR-ALPHA;

HEPATITIS C VIRUS;

EID: 79957855239     PISSN: 01615890     EISSN: 18729142     Source Type: Journal    
DOI: 10.1016/j.molimm.2011.04.008     Document Type: Article

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