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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
1989-9-13
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pubmed:abstractText |
EBV can induce human B cells to proliferate, differentiate, and undergo transformation into continuously growing lymphoblastoid cell lines. The EBV responsiveness appears to be confined to a very limited subpopulation of B cells, the nature of which is still unclear. In these studies, we sorted tonsillar B cells on the basis of their expression of the early surface activation Ag, Bac-1, and compared their proliferative responses to EBV. Bac-1+ cells responded to EBV with a relatively high level of DNA synthesis, whereas the Bac-1- cells did not. Both large and small Bac-1+ cells were responsive to EBV and the responsiveness was unrelated to the level of Bac-1 immunofluorescence intensity. Bac-1+ cells were relatively enriched for surface IgM and IgD expression. When the Bac-1- population was enriched for IgM+ cells, the proliferative response was still significantly lower than that of the Bac-1+ population. B cells acquire the ability to bind IgM relatively late after activation, and this feature did not distinguish the EBV-responsive B cells. The results suggest B cells become responsive to EBV after an early activation signal.
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pubmed:grant | |
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, Surface,
http://linkedlifedata.com/resource/pubmed/chemical/DNA,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin D,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin M,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Antigen, B-Cell,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Fc,
http://linkedlifedata.com/resource/pubmed/chemical/immunoglobulin M receptor
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
143
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1543-8
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:2547870-Adult,
pubmed-meshheading:2547870-Animals,
pubmed-meshheading:2547870-Antigens, Surface,
pubmed-meshheading:2547870-B-Lymphocytes,
pubmed-meshheading:2547870-Callitrichinae,
pubmed-meshheading:2547870-Cell Line,
pubmed-meshheading:2547870-Child,
pubmed-meshheading:2547870-DNA,
pubmed-meshheading:2547870-Herpesvirus 4, Human,
pubmed-meshheading:2547870-Humans,
pubmed-meshheading:2547870-Immunoglobulin D,
pubmed-meshheading:2547870-Immunoglobulin M,
pubmed-meshheading:2547870-Lymphocyte Activation,
pubmed-meshheading:2547870-Palatine Tonsil,
pubmed-meshheading:2547870-Receptors, Antigen, B-Cell,
pubmed-meshheading:2547870-Receptors, Fc,
pubmed-meshheading:2547870-Tumor Virus Infections
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pubmed:year |
1989
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pubmed:articleTitle |
Epstein-Barr virus preferentially induces proliferation of primed B cells.
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pubmed:affiliation |
Department of Pediatrics, University of Alabama, Birmingham 35294.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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