Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2003-7-22
pubmed:abstractText
Resistance and susceptibility to Leishmania major in mice are determined by multiple genes and correlate with the preferential development of Th1 and Th2 responses, respectively. Here, we found that CD11b+ dendritic cells (DCs) prime parasite-specific CD4+ T cells in both susceptible BALB/c (H2-d) and resistant B10.D2 (H2-d) mice. However, BALB/c and B10.D2 DCs from L. major-infected mice differ in their ability to polarize naive T cells into Th1 or Th2 effector cells. This difference is cell-intrinsic, is not restricted to H2-d mice, and is observed with both parasite-specific and allospecific CD4+ T cells. Thus, strain-specific differences within CD11b+ DCs influence the ability of inbred mice to mount polarized CD4+ T cell responses.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-10508279, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-10545503, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-10847770, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-11093169, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-11163193, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-11242036, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-11371351, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-11441078, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-11591754, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-11869679, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-11910893, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-12538655, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-12860934, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-1601029, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-1871133, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-7527824, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-7534215, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-7612219, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-7725103, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-7869047, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-7905017, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-8325337, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-8421175, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-8584935, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-8642279, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-8832890, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-9143690, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-9151907, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-9175833, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-9182685, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-9253713, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-9257839, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-9692874, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-9721100, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-9743526, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-9782133, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-9858515, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-9889960, http://linkedlifedata.com/resource/pubmed/commentcorrection/12860929-9973388
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0022-1007
pubmed:author
pubmed:issnType
Print
pubmed:day
21
pubmed:volume
198
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
201-9
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed-meshheading:12860929-Animals, pubmed-meshheading:12860929-CD4-Positive T-Lymphocytes, pubmed-meshheading:12860929-Cell Polarity, pubmed-meshheading:12860929-Cytokines, pubmed-meshheading:12860929-Dendritic Cells, pubmed-meshheading:12860929-Disease Susceptibility, pubmed-meshheading:12860929-Histocompatibility Antigens Class II, pubmed-meshheading:12860929-Immunity, Innate, pubmed-meshheading:12860929-Leishmaniasis, Cutaneous, pubmed-meshheading:12860929-Major Histocompatibility Complex, pubmed-meshheading:12860929-Mice, pubmed-meshheading:12860929-Mice, Inbred BALB C, pubmed-meshheading:12860929-Mice, Inbred Strains, pubmed-meshheading:12860929-RNA, Messenger, pubmed-meshheading:12860929-Species Specificity, pubmed-meshheading:12860929-Th1 Cells, pubmed-meshheading:12860929-Th2 Cells
pubmed:year
2003
pubmed:articleTitle
CD4+ T cell polarization in mice is modulated by strain-specific major histocompatibility complex-independent differences within dendritic cells.
pubmed:affiliation
E03-44, Institut National de la Santé et de la Recherche Médicale, University of Nice-Sophia Antipolis, 660 Route des Lucioles, 06560 Valbonne, France.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't