Source:http://linkedlifedata.com/resource/pubmed/id/10653856
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
2000-4-24
|
pubmed:abstractText |
We have generated a panel of cross-reactive T cells by immunizing SJL mice (I-A(s)) with Q144 peptide, an analog of an autoantigenic peptide (W144) of myelin proteolipid protein (PLP) 139-151 (HSLGKWLGHPDKF) in which W was replaced by Q at position 144. Following immunization with Q144, T cells were expanded in vitro with W144, which is a cross-reactive, suboptimal ligand, for Q144-specific T cells. The T cell clones responded to both ligands and grew normally on the peptide W144, but were hyperstimulated when activated by Q144 in vitro. This hyperstimulation results in a heteroclitic proliferative response with secretion of additional cytokines not induced by W144. Thus expansion of T cells by a suboptimal cross-reactive ligand effectively lowers the activation threshold so that the immunizing antigen becomes a hyperstimulating ligand for the clones. Surprisingly, when the T cell clones are grown on the hyperstimulating ligand Q144, some adapt by increasing their activation threshold. This desensitization results in a loss of response to a number of cross-reactive ligands and the appearance of a more specific T cell response. Long-term culture with the hyperstimulating ligand is sometimes associated with down-regulation of CD4 expression. These results provide an explanation for the common finding of T cell heteroclicity, and suggest that although the specificity and hierarchy of the response of T cells to peptides is determined by the TCR, activation threshold and effector functions are modified by exposure to cross-reactive ligands. This observation has implications for the development and regulation of autoimmune disease.
|
pubmed:grant | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD4,
http://linkedlifedata.com/resource/pubmed/chemical/Ligands,
http://linkedlifedata.com/resource/pubmed/chemical/Myelin Proteolipid Protein,
http://linkedlifedata.com/resource/pubmed/chemical/Peptide Fragments,
http://linkedlifedata.com/resource/pubmed/chemical/Peptides,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Antigen, T-Cell,
http://linkedlifedata.com/resource/pubmed/chemical/myelin proteolipid protein (139-151)
|
pubmed:status |
MEDLINE
|
pubmed:month |
Feb
|
pubmed:issn |
0953-8178
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
12
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
205-13
|
pubmed:dateRevised |
2011-8-26
|
pubmed:meshHeading |
pubmed-meshheading:10653856-Animals,
pubmed-meshheading:10653856-Antigens,
pubmed-meshheading:10653856-Antigens, CD4,
pubmed-meshheading:10653856-Clone Cells,
pubmed-meshheading:10653856-Cross Reactions,
pubmed-meshheading:10653856-Female,
pubmed-meshheading:10653856-Flow Cytometry,
pubmed-meshheading:10653856-Ligands,
pubmed-meshheading:10653856-Lymphocyte Activation,
pubmed-meshheading:10653856-Mice,
pubmed-meshheading:10653856-Myelin Proteolipid Protein,
pubmed-meshheading:10653856-Peptide Fragments,
pubmed-meshheading:10653856-Peptides,
pubmed-meshheading:10653856-Phenotype,
pubmed-meshheading:10653856-Receptors, Antigen, T-Cell,
pubmed-meshheading:10653856-T-Lymphocytes
|
pubmed:year |
2000
|
pubmed:articleTitle |
Tuning T cell activation threshold and effector function with cross-reactive peptide ligands.
|
pubmed:affiliation |
Center for Neurologic Diseases, Brigham and Women's Hospital and Harvard Medical School, 77 Avenue Louis Pasteur, Boston, MA 02115, USA.
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
|