Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
1982-7-19
pubmed:abstractText
A single intraperitoneal injection of the monovalent synthetic antigen, tyrosinated trimethylaminoaniline [tyr(TMA)] in Freund's complete adjuvant induces an antiidiotypic second-order T suppressor (Ts2) cell population 6 wk later. This population was able to suppress TMA-specific delayed-type hypersensitivity (DTH) responses when adoptively transferred into normal syngeneic recipients. However, they failed to function intrinsically. The inability of the Ts2 to function intrinsically was not caused by compensating idiotype-negative T cells that mediate DTH. Rather, this paradoxical observation was found to be caused by the absence or loss of function of a critical modulatory T cell population in the suppressor cell-bearing mice. This cell is functionally active in normal mice immunized for DTH responses and is sensitive to cyclophosphamide treatment. In addition, this cell type bears idiotype on its surface and is Thy-1+ and Lyt-1-,2+. It was demonstrated that by adoptively transferring the activated modulatory T cells from normal mice into tyr(TMA)-immune recipients, it was possible to observe suppressor cell function intrinsically. The potential importance of modulatory T cell function in the regulation of antibody and DTH responses is discussed.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/6210741-1117258, http://linkedlifedata.com/resource/pubmed/commentcorrection/6210741-306925, http://linkedlifedata.com/resource/pubmed/commentcorrection/6210741-308883, http://linkedlifedata.com/resource/pubmed/commentcorrection/6210741-308970, http://linkedlifedata.com/resource/pubmed/commentcorrection/6210741-313902, http://linkedlifedata.com/resource/pubmed/commentcorrection/6210741-4142565, http://linkedlifedata.com/resource/pubmed/commentcorrection/6210741-6153672, http://linkedlifedata.com/resource/pubmed/commentcorrection/6210741-6154584, http://linkedlifedata.com/resource/pubmed/commentcorrection/6210741-6164730, http://linkedlifedata.com/resource/pubmed/commentcorrection/6210741-6169780, http://linkedlifedata.com/resource/pubmed/commentcorrection/6210741-6172534, http://linkedlifedata.com/resource/pubmed/commentcorrection/6210741-6444660, http://linkedlifedata.com/resource/pubmed/commentcorrection/6210741-6445395, http://linkedlifedata.com/resource/pubmed/commentcorrection/6210741-6454741, http://linkedlifedata.com/resource/pubmed/commentcorrection/6210741-6454748, http://linkedlifedata.com/resource/pubmed/commentcorrection/6210741-6454751, http://linkedlifedata.com/resource/pubmed/commentcorrection/6210741-6454752, http://linkedlifedata.com/resource/pubmed/commentcorrection/6210741-6455299, http://linkedlifedata.com/resource/pubmed/commentcorrection/6210741-6765967, http://linkedlifedata.com/resource/pubmed/commentcorrection/6210741-6783830, http://linkedlifedata.com/resource/pubmed/commentcorrection/6210741-68972, http://linkedlifedata.com/resource/pubmed/commentcorrection/6210741-6968816, http://linkedlifedata.com/resource/pubmed/commentcorrection/6210741-6972088, http://linkedlifedata.com/resource/pubmed/commentcorrection/6210741-6997378, http://linkedlifedata.com/resource/pubmed/commentcorrection/6210741-6997388, http://linkedlifedata.com/resource/pubmed/commentcorrection/6210741-7035601, http://linkedlifedata.com/resource/pubmed/commentcorrection/6210741-80953, http://linkedlifedata.com/resource/pubmed/commentcorrection/6210741-85681, http://linkedlifedata.com/resource/pubmed/commentcorrection/6210741-87487, http://linkedlifedata.com/resource/pubmed/commentcorrection/6210741-93548
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0022-1007
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
155
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1810-22
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
1982
pubmed:articleTitle
Hapten-specific responses to the phenyltrimethylamino hapten. III. Mice whose delayed-type hypersensitivity responses cannot be abrogated by the presence of anti-idiotypic suppressor T cells lack a critical modulatory T cell function.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't