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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
3
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pubmed:dateCreated |
2001-2-26
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pubmed:abstractText |
An immunoglobulin G (IgG)-coated surface, such as that found on helminth parasites, is one of the most effective physiologic stimuli for eosinophil activation. The cysteine proteases secreted by tissue-invasive helminth larvae play an important role in evasion of the immune response by degrading the host immunoglobulins. In this study, we investigated whether cysteine proteases in the excretory-secretory product (ESP) produced by Paragonimus westermani newly excysted metacercariae (PwNEM), which cause pulmonary or extrapulmonary paragonimiasis in human beings, could modify effector functions of human eosinophils stimulated with IgG. We coated 96-well plates with human IgG in the absence or presence of the ESP produced by PwNEM. When eosinophils were incubated in the wells coated with IgG in the presence of the ESP, eosinophil degranulation and superoxide production were significantly reduced compared with results for cells incubated in wells coated with IgG alone. This inhibitory effect of the ESP on IgG-induced superoxide production was dose dependent and was significantly abolished by pretreatment of the ESP with heat. These findings suggest that the cysteine proteases secreted by PwNEM attenuate both activation and degranulation of eosinophils stimulated with IgG. Thus, the cysteine proteases produced by tissue-invasive helminth larvae play crucial roles in evasion of IgG-dependent eosinophil helminthotoxicity and in reduction of eosinophil-associated tissue inflammation during the migratory period.
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-10188385,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-10338513,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-10673346,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-10689327,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-10743354,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-10756213,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-11012979,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-1153011,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-15275116,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-1968426,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-2123226,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-2312166,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-2541198,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-2926137,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-3304826,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-3538819,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-3598802,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-3601445,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-4080419,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-564249,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-570202,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-6363816,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-6718049,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-7043200,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-7544379,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-7707186,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-7769121,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-7831096,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-7834240,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-8114830,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-8757214,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-8898333,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-9241989,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-9379296,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-9572052,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11179333-9916122
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0019-9567
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
69
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1599-604
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
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pubmed:year |
2001
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pubmed:articleTitle |
Cysteine protease secreted by Paragonimus westermani attenuates effector functions of human eosinophils stimulated with immunoglobulin G.
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pubmed:affiliation |
Department of Parasitology, College of Medicine, Ewha Woman's University, Seoul 158-710, Korea. mhshin@mm.ewha.ac.kr
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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