Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
11
pubmed:dateCreated
1994-1-6
pubmed:databankReference
pubmed:abstractText
SLE and mixed connective tissue disease (MCTD) are characterized by the presence of high titers of autoantibodies against uridine-rich RNA-small nuclear ribonucleoprotein (snRNP) Ag. Because the presence of such snRNP-reactive autoantibodies has recently been shown to be associated with polymorphisms of HLA, this study was undertaken to determine whether snRNP-reactive T cells could be identified and characterized from patients. PBMC were stimulated with affinity-purified snRNP Ag and cloned by limiting dilution in the presence of rIL-2 and rIL-4, snRNP-reactive human T cell clones were generated from three patients and two healthy blood donors who possessed disease-associated HLA genotypes. The cell surface phenotype of clones determined by flow cytometry was CD3+, CD4+, CD45RO+, TCR V alpha beta+. TCR V beta analysis, performed using V beta-specific primers and polymerase chain reaction, revealed that the T cell lines generated were clonal; a limited number of TCR V beta genes were expressed among the clones tested. All clones tested by mAb blocking of Ag-induced proliferation were restricted by HLA-DR. Several T cell clones were identified that were specific for B'/B or D polypeptides. These results demonstrate that snRNP-reactive T cells can be isolated from SLE and MCTD patients in vitro, and that Ag-driven expansion of such T cells could play a role in the immunopathogenesis of these diseases in vivo.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0022-1767
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
151
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
6460-9
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:8245479-Adult, pubmed-meshheading:8245479-Amino Acid Sequence, pubmed-meshheading:8245479-Antibodies, Monoclonal, pubmed-meshheading:8245479-Antigen-Presenting Cells, pubmed-meshheading:8245479-Base Sequence, pubmed-meshheading:8245479-Cell Line, pubmed-meshheading:8245479-Clone Cells, pubmed-meshheading:8245479-Female, pubmed-meshheading:8245479-HLA-DR Antigens, pubmed-meshheading:8245479-Humans, pubmed-meshheading:8245479-Lupus Erythematosus, Systemic, pubmed-meshheading:8245479-Lymphocyte Activation, pubmed-meshheading:8245479-Male, pubmed-meshheading:8245479-Middle Aged, pubmed-meshheading:8245479-Mixed Connective Tissue Disease, pubmed-meshheading:8245479-Molecular Sequence Data, pubmed-meshheading:8245479-Receptors, Antigen, T-Cell, alpha-beta, pubmed-meshheading:8245479-Ribonucleoproteins, Small Nuclear, pubmed-meshheading:8245479-T-Lymphocytes
pubmed:year
1993
pubmed:articleTitle
Human T cell clones reactive against U-small nuclear ribonucleoprotein autoantigens from connective tissue disease patients and healthy individuals.
pubmed:affiliation
Department of Internal Medicine, University of Missouri-Columbia School of Medicine.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, U.S. Gov't, Non-P.H.S.