CXCR3 ligands contribute to Th1-induced inflammation but not to homing of Th1 cells into the lung

Experimental Lung Research

Volumn 34, Issue 7, 2008, Pages 391-407

  Manicone, Anne M ^a,c   Burkhart, Kristi M ^a   Lu, Bao ^b   Clark, Joan G ^c  

^a UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

^b BOSTON CHILDREN S HOSPITAL   (United States)

^c UNIVERSITY OF WASHINGTON   (United States)

Author keywords

IP10; Macrophage; MIG

Indexed keywords

CHEMOKINE RECEPTOR CXCR3; CXCL9 CHEMOKINE; GAMMA INTERFERON INDUCIBLE PROTEIN 10; NEUTRALIZING ANTIBODY;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELL ACTIVITY; CELL HOMING; CELL PROLIFERATION; CELL TRANSPORT; CONTROLLED STUDY; HOST CELL; IN VITRO STUDY; INFLAMMATION; MOUSE; NONHUMAN; PNEUMONIA; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTEIN INTERACTION; TH1 CELL;

ADOPTIVE TRANSFER; ANIMALS; ANTIBODIES; CELL PROLIFERATION; CELLS, CULTURED; CHEMOKINE CXCL10; CHEMOKINE CXCL9; CHEMOTAXIS, LEUKOCYTE; DISEASE MODELS, ANIMAL; LIGANDS; LUNG; MACROPHAGES, ALVEOLAR; MICE; MICE, INBRED C57BL; MICE, KNOCKOUT; PNEUMONIA; RECEPTORS, CXCR3; RECOMBINANT PROTEINS; TH1 CELLS; TIME FACTORS;

EID: 50049118687     PISSN: 01902148     EISSN: 15210499     Source Type: Journal    
DOI: 10.1080/01902140802221987     Document Type: Article

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