Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
7
pubmed:dateCreated
2003-6-23
pubmed:abstractText
Morbidity and mortality in schistosomiasis are largely due to an immune response mediated by CD4 T lymphocytes. Since lymphocyte activation is shaped by costimulatory signals, the specific functions of different costimulatory pathways are of increasing interest. We now examined the role of the inducible costimulatory molecule (ICOS) and its ligand B7-related protein 1 (B7RP-1) in the experimental murine schistosome infection by blocking this costimulatory pathway with monoclonal antibody against ICOS, administered daily by intraperitoneal injection during the patent phase of the disease. The treated mice exhibited enhanced hepatic immunopathology characterized by enlarged egg granulomas and pronounced parenchymal inflammation with hepatocellular necrosis, resulting in elevated liver enzyme levels in serum. Most strikingly, there was a sharp increase in gamma interferon (IFN-gamma) production by schistosome egg antigen-stimulated granuloma cells, bulk mesenteric lymph node (MLN) cells, and purified MLN CD4 T cells, which contrasted with a more discreet change in the Th2-type cytokines interleukin 4 (IL-4) and IL-10. These findings suggest that the ICOS-B7RP-1 costimulatory pathway serves primarily to control IFN-gamma production, thereby promoting a cytokine environment conducive to limited hepatic damage.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-10072537, http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-10201906, http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-10760791, http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-10843696, http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-10880526, http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-10933398, http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-11046032, http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-11169414, http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-11429535, http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-11429542, http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-11429543, http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-11429544, http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-11489981, http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-11606762, http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-11801630, http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-11861596, http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-11971013, http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-12672053, http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-1682388, http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-1824635, http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-2504481, http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-3096893, http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-3111283, http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-5535626, http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-7525726, http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-7737289, http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-8335939, http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-839071, http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-8617955, http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-8671630, http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-8717514, http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-9174607, http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-9651922, http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-9709038, http://linkedlifedata.com/resource/pubmed/commentcorrection/12819093-9930702
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0019-9567
pubmed:author
pubmed:issnType
Print
pubmed:volume
71
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
4040-4
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed:year
2003
pubmed:articleTitle
Disruption of the ICOS-B7RP-1 costimulatory pathway leads to enhanced hepatic immunopathology and increased gamma interferon production by CD4 T cells in murine schistosomiasis.
pubmed:affiliation
Department of Pathology, Tufts University School of Medicine, Boston, Massachusetts 02111, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.