Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
1983-4-15
pubmed:abstractText
We have previously shown that lymphoblasts alloactivated in vitro acquire the capacity of stimulating the autologous mixed lymphocyte response. This response is anti-idiotypic in nature because lymphocytes so primed display accelerated memory responses only when restimulated by autologous lymphoblasts that have been alloactivated against the same HLA-DR antigen. Based on this observation we have postulated that the absence of HLA antibodies in alloimmunized human subjects may be due to the development of autoantibodies that react with the anti-HLA receptors expressed by primed lymphocytes or by anti-HLA antibodies or both. This hypothesis has been confirmed in the present investigations which show that sera from parous women react with autologous T lymphoblasts primed in 5-day mixed lymphocyte culture against their husband-i.e., with lymphoblasts expressing receptors for the immunizing donor. Anti-HLA receptors expressed by T and B lymphocytes seem to share serologic determinants because sera that bind to autologous alloactivated lymphoblasts are also capable of inhibiting the anti-HLA activity of autologous and homologous sera. Auto-anti-idiotypic antibodies inhibit the autologous mixed lymphocyte response to autologous alloactivated lymphoblasts, a phenomenon whose in vivo correlate may reside in autoinhibition of anti-HLA antibody formation and of allograft immunity. Because auto-anti-idiotypic antibodies were found in sera from all parous women tested, the hypothesis that nonresponsiveness to alloantigens exists as a state per se is not likely. The passive transfer of antireceptor (idiotype) immunity by use of antibodies from pregnant women's sera may provide a powerful tool for specific suppression of allograft rejection.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/6600840-10649, http://linkedlifedata.com/resource/pubmed/commentcorrection/6600840-331569, http://linkedlifedata.com/resource/pubmed/commentcorrection/6600840-33224, http://linkedlifedata.com/resource/pubmed/commentcorrection/6600840-408091, http://linkedlifedata.com/resource/pubmed/commentcorrection/6600840-4270240, http://linkedlifedata.com/resource/pubmed/commentcorrection/6600840-6161968, http://linkedlifedata.com/resource/pubmed/commentcorrection/6600840-6173456, http://linkedlifedata.com/resource/pubmed/commentcorrection/6600840-6174671, http://linkedlifedata.com/resource/pubmed/commentcorrection/6600840-6177823, http://linkedlifedata.com/resource/pubmed/commentcorrection/6600840-6808075, http://linkedlifedata.com/resource/pubmed/commentcorrection/6600840-6946986, http://linkedlifedata.com/resource/pubmed/commentcorrection/6600840-69518, http://linkedlifedata.com/resource/pubmed/commentcorrection/6600840-6968909, http://linkedlifedata.com/resource/pubmed/commentcorrection/6600840-7051480
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0027-8424
pubmed:author
pubmed:issnType
Print
pubmed:volume
80
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
830-4
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
1983
pubmed:articleTitle
Anti-idiotypic antibodies to anti-HLA receptors induced by pregnancy.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.