IL-10 is crucial for the transition from acute to chronic disease state during infection of mice with Schistosoma mansoni

European Journal of Immunology

Volumn 33, Issue 4, 2003, Pages 880-888

  Sadler, Clare H ^a   Rutitzky, Laura I ^b   Stadecker, Miguel J ^b   Wilson, R Alan ^a  

^a UNIVERSITY OF YORK   (United Kingdom)

^b TUFTS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Inflammation; Parasitic helminth; Rodent; Suppression

Indexed keywords

COLLAGEN; GAMMA INTERFERON; INTERLEUKIN 10; INTERLEUKIN 4; PARASITE ANTIGEN;

ACUTE DISEASE; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; CELL INFILTRATION; CHRONIC DISEASE; CONTROLLED STUDY; CYTOKINE PRODUCTION; DISEASE ACTIVITY; GRANULOMA; HEPATITIS; IMMUNOMODULATION; IMMUNOPATHOLOGY; IMMUNOREGULATION; IN VITRO STUDY; INTESTINE WALL; LIVER; LIVER NECROSIS; LYMPH NODE; LYMPHOCYTE PROLIFERATION; MOUSE; NONHUMAN; PRIORITY JOURNAL; REVIEW; SCHISTOSOMA MANSONI; SCHISTOSOMIASIS; SPLEEN CELL; T LYMPHOCYTE ACTIVATION; TUMOR EMBOLISM; TUMOR VOLUME; WILD TYPE;

ACUTE DISEASE; ANIMALS; ANTIBODIES, HELMINTH; ANTIGENS, HELMINTH; CD4-POSITIVE T-LYMPHOCYTES; CELLS, CULTURED; CHRONIC DISEASE; CYTOKINES; DISEASE PROGRESSION; GRANULOMA; INTERLEUKIN-10; LYMPHOCYTE ACTIVATION; MICE; MICE, INBRED C57BL; MICE, KNOCKOUT; SCHISTOSOMA MANSONI; SCHISTOSOMIASIS MANSONI;

EID: 0038476617     PISSN: 00142980     EISSN: None     Source Type: Journal    
DOI: 10.1002/eji.200323501     Document Type: Review

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