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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0015576,
umls-concept:C0039194,
umls-concept:C0054941,
umls-concept:C0086418,
umls-concept:C0206431,
umls-concept:C0332120,
umls-concept:C0443288,
umls-concept:C0680022,
umls-concept:C0871261,
umls-concept:C1413207,
umls-concept:C1413209,
umls-concept:C1704632,
umls-concept:C1706817,
umls-concept:C2911692
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pubmed:issue |
7
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pubmed:dateCreated |
1996-11-25
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pubmed:abstractText |
Previous studies suggest that CD1 is a family of Ag-presenting molecules distantly related to those encoded by the MHC. However, of the four known human CD1 proteins, only CD1b has been shown to restrict Ag-specific T cell responses. In this study, we have shown that a second member of the human CD1 family, CD1c, could also mediate Ag presentation to T cells. Three T cell lines recognizing mycobacterial Ags in a CD1c-restricted manner were isolated from normal donor blood. These T cells were MHC unrestricted, and their recognition of Ag was independent of the products of the transporter associated with Ag presentation-1/2 and DMA/B genes that are generally required for Ag presentation by MHC-encoded Ag-presenting molecules. Furthermore, unlike MHC-restricted responses to peptides, the CD1c-restricted T cell lines recognized protease-resistant mycobacterial lipid Ags. These T cell lines also showed significant cytotoxicity toward CD1c-expressing target cells even in the absence of mycobacterial Ags, which was shown by clonal analysis to be mediated by a subpopulation of T cells directly reactive to CD1c molecules. Our findings establish the ability of a second member of the CD1 family to restrict responses of Ag-specific T cells, and thus support the general hypothesis that the CD1 family comprises a third lineage of Ag-presenting molecules that presents a novel class of foreign and self Ags to MHC-unrestricted T cells.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Bacterial,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD1,
http://linkedlifedata.com/resource/pubmed/chemical/Lipopolysaccharides,
http://linkedlifedata.com/resource/pubmed/chemical/Mannosides,
http://linkedlifedata.com/resource/pubmed/chemical/Membrane Glycoproteins,
http://linkedlifedata.com/resource/pubmed/chemical/Phosphatidylinositols,
http://linkedlifedata.com/resource/pubmed/chemical/lipoarabinomannan
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
157
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2795-803
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:8816382-Antigen Presentation,
pubmed-meshheading:8816382-Antigens, Bacterial,
pubmed-meshheading:8816382-Antigens, CD1,
pubmed-meshheading:8816382-Cell Line,
pubmed-meshheading:8816382-Humans,
pubmed-meshheading:8816382-Lipopolysaccharides,
pubmed-meshheading:8816382-Mannosides,
pubmed-meshheading:8816382-Membrane Glycoproteins,
pubmed-meshheading:8816382-Mycobacterium tuberculosis,
pubmed-meshheading:8816382-Phosphatidylinositols,
pubmed-meshheading:8816382-T-Lymphocyte Subsets
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pubmed:year |
1996
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pubmed:articleTitle |
CD1c restricts responses of mycobacteria-specific T cells. Evidence for antigen presentation by a second member of the human CD1 family.
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pubmed:affiliation |
Division of Rheumatology and Immunology, Brigham and Women's Hospital, Boston, MA 02115, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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