Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
1979-9-17
pubmed:abstractText
The present study describes the qualitative reactions of a xenogeneic anti-idiotype (Id) antiserum produced in a mouse-gamma-globulin-tolerant rabbit (5,936) against B6 anti-CBA IgG antibodies. The results showed that such an anti-Id antiserum reacts specifically against anti-H-2k antibodies and against H-2k alloantigen-activated T cells from the following pairs of congenic mice: B10 (H-2b) and B10.D2 (H-2d); and A.BY (H-2b) and A.SW (H-2s), but not against C3H.SW (H-2b) and C3H.OH (H-2o); and BALB/b (H-2b) and BALB/c (H-2d). CB 20 (BALB/c mice with the Ig-1b allotype) anti-CBA T blasts also express idiotypic determinants that react with rabbit 5,936 antiserum. Thus, positive reactions are obtained between rabbit 5,936 anti-Id antiserum and anti-H-2k IgG preparations and T blasts from mice carrying the Ig-1b or Ig-1e allotype, but not from mice carrying the Ig-1a allotype. These reactions are qualitatively independent of the H-2 genotype of the Id-producing mice. Such a finding strongly suggests that the Id-bearing receptor molecules on mouse T cells are coded for by genes that are associated with the Ig heavy-chain-linkage group and not to the mouse histocompatibility complex. Furthermore, the anti-Id antibodies studied react preferentially against anti-H-2k antibodies or T cells with specificity toward the IAk-region-associated serological specificities. Thus, genes associated with the Ig heavy-chain-linkage group seem to be structural genes for at least T-cell receptors with specificity for IA-region-coded membrane antigens.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/110903-100785, http://linkedlifedata.com/resource/pubmed/commentcorrection/110903-103727, http://linkedlifedata.com/resource/pubmed/commentcorrection/110903-302186, http://linkedlifedata.com/resource/pubmed/commentcorrection/110903-302982, http://linkedlifedata.com/resource/pubmed/commentcorrection/110903-303266, http://linkedlifedata.com/resource/pubmed/commentcorrection/110903-305612, http://linkedlifedata.com/resource/pubmed/commentcorrection/110903-307689, http://linkedlifedata.com/resource/pubmed/commentcorrection/110903-322367, http://linkedlifedata.com/resource/pubmed/commentcorrection/110903-408092, http://linkedlifedata.com/resource/pubmed/commentcorrection/110903-412192, http://linkedlifedata.com/resource/pubmed/commentcorrection/110903-412775, http://linkedlifedata.com/resource/pubmed/commentcorrection/110903-413058, http://linkedlifedata.com/resource/pubmed/commentcorrection/110903-4136037, http://linkedlifedata.com/resource/pubmed/commentcorrection/110903-4136845, http://linkedlifedata.com/resource/pubmed/commentcorrection/110903-4540327, http://linkedlifedata.com/resource/pubmed/commentcorrection/110903-4551691, http://linkedlifedata.com/resource/pubmed/commentcorrection/110903-52178, http://linkedlifedata.com/resource/pubmed/commentcorrection/110903-60781, http://linkedlifedata.com/resource/pubmed/commentcorrection/110903-63988, http://linkedlifedata.com/resource/pubmed/commentcorrection/110903-66781, http://linkedlifedata.com/resource/pubmed/commentcorrection/110903-69514, http://linkedlifedata.com/resource/pubmed/commentcorrection/110903-69518, http://linkedlifedata.com/resource/pubmed/commentcorrection/110903-825450, http://linkedlifedata.com/resource/pubmed/commentcorrection/110903-83961, http://linkedlifedata.com/resource/pubmed/commentcorrection/110903-96442
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0022-1007
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
150
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
307-21
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed:year
1979
pubmed:articleTitle
Alloantigen-specific idiotype-bearing receptors on mouse T lymphocytes. I. Specificity characterization and genetic association with the heavy-chain IgG allotype.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.