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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1985-4-1
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pubmed:abstractText |
The cellular requirements for stimulating primed alloreactive T cells have been investigated. In vitro-primed secondary alloreactive cells, long-term lines, and Ly 1+2- noncytolytic clones which reacted with allo-H-2K, D, or Mls (M locus) antigens were tested. The data indicated that a specialized antigen-presenting cell such as a macrophage or a dendritic cell was required for stimulating primed alloreactive cells across all the genetic disparities tested. B and T lymphocytes were ineffective stimulators. The stimulator requirement for secondary and Ly 1+2- clone responses was heterogeneous, since both macrophages and dendritic cells were effective stimulators. Thus, the allostimulator requirement for inducing proliferation and mediator secretion by the primed T-cell populations closely paralleled the requirement for stimulating unprimed populations. The only exception found was the peritoneal washout population, which did not stimulate a primary response but did stimulate secondary responses. The failure of peritoneal macrophages to stimulate a primary response was shown to be due to an inhibitory pathway which did not occur when the responding population was alloantigen primed.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Monoclonal,
http://linkedlifedata.com/resource/pubmed/chemical/H-2 Antigens,
http://linkedlifedata.com/resource/pubmed/chemical/Histocompatibility Antigens Class II,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Antigen, B-Cell,
http://linkedlifedata.com/resource/pubmed/chemical/histocompatibility antigen H-2D(b)
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0008-8749
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
91
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
60-74
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:3156000-Animals,
pubmed-meshheading:3156000-Antibodies, Monoclonal,
pubmed-meshheading:3156000-Antigen-Presenting Cells,
pubmed-meshheading:3156000-Binding, Competitive,
pubmed-meshheading:3156000-Cell Adhesion,
pubmed-meshheading:3156000-Clone Cells,
pubmed-meshheading:3156000-H-2 Antigens,
pubmed-meshheading:3156000-Haploidy,
pubmed-meshheading:3156000-Histocompatibility Antigens Class II,
pubmed-meshheading:3156000-Lymphocyte Activation,
pubmed-meshheading:3156000-Lymphocyte Culture Test, Mixed,
pubmed-meshheading:3156000-Macrophages,
pubmed-meshheading:3156000-Mice,
pubmed-meshheading:3156000-Mice, Inbred C57BL,
pubmed-meshheading:3156000-Mice, Inbred DBA,
pubmed-meshheading:3156000-Peritoneal Cavity,
pubmed-meshheading:3156000-Receptors, Antigen, B-Cell,
pubmed-meshheading:3156000-Spleen,
pubmed-meshheading:3156000-T-Lymphocytes
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pubmed:year |
1985
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pubmed:articleTitle |
Stimulator requirements for primed alloreactive T cells: macrophages and dendritic cells activate T cells across all genetic disparities.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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