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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0018951,
umls-concept:C0019764,
umls-concept:C0021467,
umls-concept:C0021469,
umls-concept:C0024264,
umls-concept:C0085358,
umls-concept:C0086418,
umls-concept:C0108779,
umls-concept:C0205307,
umls-concept:C0376152,
umls-concept:C1332717,
umls-concept:C1413244,
umls-concept:C1533691,
umls-concept:C1706438,
umls-concept:C2698600
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pubmed:issue |
5
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pubmed:dateCreated |
1988-12-8
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pubmed:abstractText |
We previously demonstrated that after allogeneic bone marrow transplantation (BMT) a subset of CD8, HNK1, and DR-positive T lymphocytes are able to inhibit CFU-GM and BFU-E growth with an HLA-DR restriction. In this study we investigated whether these cells, present in normal marrow in low concentration (less than 1%), play the same role. HNK1-positive sorted marrow cells forming rosettes (E+C) were able to inhibit BFU-E and CFU-GM growth when added back to the marrow E-C at a ratio of 1:10 (HNK1+ E+C/E-C) in a range from 40% to 60%. This inhibitory effect was also detected for a cellular ratio of 1:100, which is the normal marrow value for this subset of T cell. HNK1+ DR+-sorted E+C after double-immunofluorescent labeling also showed the same inhibitory activity as the HNK1+ E+C, whereas the negative fraction including all the other E+C had no detectable inhibitory activity. CD3 and CD8 antigens were also present on the membrane of these cells, as demonstrated in two cases by double-immunofluorescent labeling performed with anti-CD3 or anti-CD8 monoclonal antibodies (MoAbs) and HNK1 MoAb, respectively, and subsequent cell sorting. Blocking experiments, performed by adding in culture anti-CD4 and anti-CD8 MoAbs to HNK1+ T cells showed that only the last MoAb was able to prevent inhibition of hematopoietic colony growth. These results confirmed that one subset of CD3+, CD8+, HNK1+, and DR+ T cells was responsible for in vitro inhibition of normal hematopoiesis. In addition, this inhibition was genetically restricted to HLA-class II antigens, since in three co-culture experiments with unrelated bone marrow cells inhibition occurred only when cells with one haplo-identical HLA-DR antigen was added back to the culture. Indeed, this effect was really HLA-DR restricted, since in blocking experiments with different anti-HLA class II MoAbs (anti-DR, anti-DP, and anti-DQ MoAbs) only an anti-HLA-DR MoAb was able to prevent the colony growth inhibition by CD3+ HNK1+, or CD8+ HNK1+ E+C. In conclusion, the CD3+, HNK1+, CD8+, DR+ cells may be the T-cell subset able to inhibit normal hematopoiesis with an HLA-DR restriction.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD3,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD8,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Differentiation...,
http://linkedlifedata.com/resource/pubmed/chemical/HLA-DR Antigens,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Antigen, T-Cell
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0006-4971
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
72
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1616-21
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:2972326-Antigens, CD3,
pubmed-meshheading:2972326-Antigens, CD8,
pubmed-meshheading:2972326-Antigens, Differentiation, T-Lymphocyte,
pubmed-meshheading:2972326-Bone Marrow Cells,
pubmed-meshheading:2972326-Cell Division,
pubmed-meshheading:2972326-Colony-Forming Units Assay,
pubmed-meshheading:2972326-Cytotoxicity, Immunologic,
pubmed-meshheading:2972326-HLA-DR Antigens,
pubmed-meshheading:2972326-Hematopoiesis,
pubmed-meshheading:2972326-Humans,
pubmed-meshheading:2972326-Immunity, Cellular,
pubmed-meshheading:2972326-Killer Cells, Natural,
pubmed-meshheading:2972326-Receptors, Antigen, T-Cell,
pubmed-meshheading:2972326-T-Lymphocytes
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pubmed:year |
1988
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pubmed:articleTitle |
In vitro inhibition of normal human hematopoiesis by marrow CD3+, CD8+, HLA-DR+, HNK1+ lymphocytes.
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pubmed:affiliation |
INSERM U.91, Service d'Hématologie Hôpital Henri Mondor, Créteil, France.
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pubmed:publicationType |
Journal Article,
In Vitro,
Research Support, Non-U.S. Gov't
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