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PredicateObject
rdf:type
lifeskim:mentions
pubmed:dateCreated
1994-12-27
pubmed:abstractText
We used synthetic peptides duplicating the structures of a human lambda light chain (Mcg), and a human T-cell receptor (Tcr) alpha and a Tcr beta chain predicted from gene sequence to determine the presence and loci of activity of natural human autoantibodies directed against these antigen recognition molecules. We report that normal individuals and patients suffering from autoimmune diseases have antibodies directed against regions of lambda light chains and Tcr beta chains corresponding to the first complementarity determining region and the third framework region of the variable domain and to constant region determinants. The levels of IgM natural antibodies particularly against the CDR1 peptides tend to be higher in RA patients than in normals or SLE patients. Although polyclonal IgG immunoglobulins from healthy individuals did not show detectable reactivity to Tcr alpha peptides, such reactivity was found in the IgM immunoglobulins of RA patients, thereby showing that Tcr alpha peptides can be autoantigenic in man. The levels of IgM autoantibodies to V beta CDR1 peptides tend to decrease with age. By contrast, there was a marked increase in IgG natural autoantibodies to certain CDR1 sequences with advancing age. We suggest that the natural antibodies to defined regions of immunoglobulins and T-cell receptors are part of a physiological network for the regulation of the immune response.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
0065-2598
pubmed:author
pubmed:issnType
Print
pubmed:volume
347
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
135-45
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:7976728-Adult, pubmed-meshheading:7976728-Aged, pubmed-meshheading:7976728-Aged, 80 and over, pubmed-meshheading:7976728-Aging, pubmed-meshheading:7976728-Amino Acid Sequence, pubmed-meshheading:7976728-Animals, pubmed-meshheading:7976728-Antibody Specificity, pubmed-meshheading:7976728-Arthritis, Rheumatoid, pubmed-meshheading:7976728-Autoantibodies, pubmed-meshheading:7976728-Autoantigens, pubmed-meshheading:7976728-Autoimmune Diseases, pubmed-meshheading:7976728-Enzyme-Linked Immunosorbent Assay, pubmed-meshheading:7976728-Humans, pubmed-meshheading:7976728-Immunoglobulin G, pubmed-meshheading:7976728-Immunoglobulin Light Chains, pubmed-meshheading:7976728-Immunoglobulin M, pubmed-meshheading:7976728-Molecular Sequence Data, pubmed-meshheading:7976728-Myeloma Proteins, pubmed-meshheading:7976728-Peptide Fragments, pubmed-meshheading:7976728-Rabbits, pubmed-meshheading:7976728-Receptors, Antigen, T-Cell, alpha-beta, pubmed-meshheading:7976728-Reference Values
pubmed:year
1994
pubmed:articleTitle
Naturally occurring human autoantibodies to defined T-cell receptor and light chain peptides.
pubmed:affiliation
Microbiology and Immunology Department, University of Arizona, Tucson 85724.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't