Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
2009-3-16
pubmed:abstractText
The levels of regulatory T cells (Treg cells), analyzed by Foxp3 mRNA expression, were determined in lesions from patients with acute cutaneous leishmaniasis (ACL) and chronic cutaneous leishmaniasis (CCL). We demonstrated that Treg cells preferentially accumulate in lesions from ACL patients during the early phase of infection (lesion duration of less than 1 month). In addition, levels of Foxp3 mRNA transcripts were significantly higher in specimens from patients with CCL than in those from patients with ACL, suggesting a critical role of intralesional Treg cells in CCL. Intralesional Treg cells from both ACL and CCL patients were shown to have suppressive functions in vitro, since they inhibited the gamma interferon (IFN-gamma) produced by CD4(+) CD25(-) T cells purified from peripheral blood mononuclear cells from the same patient in response to Leishmania guyanensis stimulation. Intralesional 2,3-indoleamine dioxygenase (IDO) mRNA expression was associated with that of Foxp3, suggesting a role for IDO in the suppressive activity of intralesional Treg cells. In addition, a role, albeit minor, of interleukin-10 (IL-10) was also demonstrated, since neutralization of IL-10 produced by intralesional T cells increased IFN-gamma production by effector cells in an in vitro suppressive assay. These results confirm the role of intralesional Treg cells in the immunopathogenesis of human Leishmania infection, particularly in CCL patients.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/19168733-10899916, http://linkedlifedata.com/resource/pubmed/commentcorrection/19168733-11716098, http://linkedlifedata.com/resource/pubmed/commentcorrection/19168733-11740743, http://linkedlifedata.com/resource/pubmed/commentcorrection/19168733-12186837, http://linkedlifedata.com/resource/pubmed/commentcorrection/19168733-12186838, http://linkedlifedata.com/resource/pubmed/commentcorrection/19168733-12218142, http://linkedlifedata.com/resource/pubmed/commentcorrection/19168733-12228717, http://linkedlifedata.com/resource/pubmed/commentcorrection/19168733-12232795, http://linkedlifedata.com/resource/pubmed/commentcorrection/19168733-12368911, http://linkedlifedata.com/resource/pubmed/commentcorrection/19168733-12466842, http://linkedlifedata.com/resource/pubmed/commentcorrection/19168733-12654849, http://linkedlifedata.com/resource/pubmed/commentcorrection/19168733-15351783, http://linkedlifedata.com/resource/pubmed/commentcorrection/19168733-15728505, http://linkedlifedata.com/resource/pubmed/commentcorrection/19168733-15905558, http://linkedlifedata.com/resource/pubmed/commentcorrection/19168733-16113310, http://linkedlifedata.com/resource/pubmed/commentcorrection/19168733-16586370, http://linkedlifedata.com/resource/pubmed/commentcorrection/19168733-16903921, http://linkedlifedata.com/resource/pubmed/commentcorrection/19168733-17283207, http://linkedlifedata.com/resource/pubmed/commentcorrection/19168733-17389235, http://linkedlifedata.com/resource/pubmed/commentcorrection/19168733-17675505, http://linkedlifedata.com/resource/pubmed/commentcorrection/19168733-17947673, http://linkedlifedata.com/resource/pubmed/commentcorrection/19168733-17948021, http://linkedlifedata.com/resource/pubmed/commentcorrection/19168733-17948274, http://linkedlifedata.com/resource/pubmed/commentcorrection/19168733-18070890, http://linkedlifedata.com/resource/pubmed/commentcorrection/19168733-18285775, http://linkedlifedata.com/resource/pubmed/commentcorrection/19168733-18424735, http://linkedlifedata.com/resource/pubmed/commentcorrection/19168733-18832696, http://linkedlifedata.com/resource/pubmed/commentcorrection/19168733-19125672, http://linkedlifedata.com/resource/pubmed/commentcorrection/19168733-2492973, http://linkedlifedata.com/resource/pubmed/commentcorrection/19168733-6422465, http://linkedlifedata.com/resource/pubmed/commentcorrection/19168733-7612219
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
1098-5522
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
77
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1465-74
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed-meshheading:19168733-Acute Disease, pubmed-meshheading:19168733-Adolescent, pubmed-meshheading:19168733-Adult, pubmed-meshheading:19168733-Animals, pubmed-meshheading:19168733-Chronic Disease, pubmed-meshheading:19168733-Female, pubmed-meshheading:19168733-Forkhead Transcription Factors, pubmed-meshheading:19168733-Humans, pubmed-meshheading:19168733-Indoleamine-Pyrrole 2,3,-Dioxygenase, pubmed-meshheading:19168733-Interferon-gamma, pubmed-meshheading:19168733-Interleukin-10, pubmed-meshheading:19168733-Leishmania guyanensis, pubmed-meshheading:19168733-Leishmaniasis, Cutaneous, pubmed-meshheading:19168733-Male, pubmed-meshheading:19168733-Middle Aged, pubmed-meshheading:19168733-RNA, Messenger, pubmed-meshheading:19168733-Skin, pubmed-meshheading:19168733-T-Lymphocytes, Regulatory, pubmed-meshheading:19168733-Young Adult
pubmed:year
2009
pubmed:articleTitle
Intralesional regulatory T-cell suppressive function during human acute and chronic cutaneous leishmaniasis due to Leishmania guyanensis.
pubmed:affiliation
Immunologie des Leishmanioses, Institut Pasteur de la Guyane, 97306 Cayenne, French Guyana.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't