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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
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pubmed:dateCreated |
1996-7-25
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pubmed:abstractText |
Humans chronically infected with schistosomiasis usually have impaired parasite Ag-specific lymphocyte proliferation and IFN-gamma production that may facilitate persistence of the parasite while producing little clinical disease. The mechanisms that contribute to the immunologic hyporesponsiveness in these patients remain undefined. IL-10 has been shown to exert an inhibitory effect on cell-mediated immunity. To determine whether endogenous IL-10 has a role in regulating parasite-specific anergy in schistosomiasis, neutralizing anti-IL-10 added to PBMC from Schistosoma haematobium patients' enhanced adult worm (SWAP)- or egg Ag (SEA)-driven lymphocyte proliferation and/or IFN-gamma production by 2- to >100-fold in 32 of 38 subjects. In contrast, anti-IL-10 failed to significantly augment the mycobacterial Ag, purified protein derivative (PPD)-driven lymphocyte proliferation, or IFN-gamma production in 9 or 10 of 14 individuals, respectively. SWAP or SEA triggered IL-10 release from PBMC of both patients and healthy individuals; however, CD4+ cells were a significant source of IL-10 only in infected subjects. PPD relative to SWAP induced fivefold less IL-10 release by CD4+ cells (p < 0.01). A possible mechanism whereby IL-10 suppressed Ag-specific T cell responses was demonstrated by the ability of SWAP and not PPD to suppress B7 expression on PBMC. Anti-IL-10 completely inhibited the parasite Ag-induced down-regulation of B7 expression. These studies indicate that IL-10 contributes to parasite Ag-induced T cell hyporesponsiveness observed in patients with chronic schistosomiasis hematobia.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jun
|
pubmed:issn |
0022-1767
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pubmed:author |
pubmed-author:BrustoskiKK,
pubmed-author:El-SherbinyMM,
pubmed-author:HelmyAA,
pubmed-author:IbrahimSS,
pubmed-author:KhaudaryJJ,
pubmed-author:KingC LCL,
pubmed-author:MalhotraII,
pubmed-author:MedhatAA,
pubmed-author:NafehMM,
pubmed-author:ShataM TMT,
pubmed-author:ShehataMM,
pubmed-author:StupiR JRJ,
pubmed-author:ZagàFF
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pubmed:issnType |
Print
|
pubmed:day |
15
|
pubmed:volume |
156
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pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
4715-21
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:8648117-Adolescent,
pubmed-meshheading:8648117-Adult,
pubmed-meshheading:8648117-Animals,
pubmed-meshheading:8648117-Antigens, Helminth,
pubmed-meshheading:8648117-Base Sequence,
pubmed-meshheading:8648117-Child,
pubmed-meshheading:8648117-Chronic Disease,
pubmed-meshheading:8648117-DNA Primers,
pubmed-meshheading:8648117-Humans,
pubmed-meshheading:8648117-Immune Tolerance,
pubmed-meshheading:8648117-Interferon-gamma,
pubmed-meshheading:8648117-Interleukin-10,
pubmed-meshheading:8648117-Lymphocyte Activation,
pubmed-meshheading:8648117-Molecular Sequence Data,
pubmed-meshheading:8648117-Schistosoma haematobium,
pubmed-meshheading:8648117-Schistosomiasis haematobia
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pubmed:year |
1996
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pubmed:articleTitle |
Cytokine control of parasite-specific anergy in human urinary schistosomiasis. IL-10 modulates lymphocyte reactivity.
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pubmed:affiliation |
Division of Geographic Medicine, Western Reserve University, Cleveland, OH 44106, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't
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