Blocking chemokine responsive to γ-2/interferon (IFN)-γ inducible protein and monokine induced by IFN-γ activity in vivo reduces the pathogenetic but not the antiviral potential of hepatitis B virus-specific cytotoxic T lymphocytes

Journal of Experimental Medicine

Volumn 194, Issue 12, 2001, Pages 1755-1766

  Kakimi, Kazuhiro ^a   Lane, Thomas E ^b   Wieland, Stefan ^a   Asensio, Valerie C ^a   Campbell, Iain L ^a   Chisari, Francis V ^a   Guidotti, Luca G ^a  

^a SCRIPPS RESEARCH INSTITUTE   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Chemokines; Hepatitis B virus; Infectious immunity virus; Liver

Indexed keywords

ANTIBODY; CHEMOKINE; CHEMOKINE RESPONSIVE TO GAMMA 2; GAMMA INTERFERON; GAMMA INTERFERON INDUCIBLE PROTEIN 10; MONOKINE; MONOKINE INDUCED BY INTERFERON GAMMA; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANTIVIRAL ACTIVITY; ARTICLE; CELL TRANSFER; CONTROLLED STUDY; CYTOKINE PRODUCTION; CYTOTOXIC T LYMPHOCYTE; DISEASE SEVERITY; HEPATITIS B; HEPATITIS B VIRUS; IMMUNOTHERAPY; IN VIVO STUDY; LIVER DISEASE; LIVER INJURY; MONONUCLEAR CELL; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; PATHOGENICITY; PRIORITY JOURNAL; TRANSGENIC MOUSE; VIRUS REPLICATION;

ANIMALS; CYTOTOXICITY, IMMUNOLOGIC; HEPATITIS B; HEPATITIS B VIRUS; INTERFERON TYPE II; LIVER; MICE; MICE, TRANSGENIC; MONOKINES; T-LYMPHOCYTES, CYTOTOXIC;

EID: 0035905411     PISSN: 00221007     EISSN: None     Source Type: Journal    
DOI: 10.1084/jem.194.12.1755     Document Type: Article

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