pubmed-article:2154620 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:2154620 | lifeskim:mentions | umls-concept:C0014644 | lld:lifeskim |
pubmed-article:2154620 | lifeskim:mentions | umls-concept:C0368761 | lld:lifeskim |
pubmed-article:2154620 | lifeskim:mentions | umls-concept:C0004561 | lld:lifeskim |
pubmed-article:2154620 | lifeskim:mentions | umls-concept:C0024432 | lld:lifeskim |
pubmed-article:2154620 | lifeskim:mentions | umls-concept:C0003320 | lld:lifeskim |
pubmed-article:2154620 | lifeskim:mentions | umls-concept:C1510411 | lld:lifeskim |
pubmed-article:2154620 | lifeskim:mentions | umls-concept:C0021467 | lld:lifeskim |
pubmed-article:2154620 | lifeskim:mentions | umls-concept:C1444748 | lld:lifeskim |
pubmed-article:2154620 | lifeskim:mentions | umls-concept:C0021469 | lld:lifeskim |
pubmed-article:2154620 | lifeskim:mentions | umls-concept:C1522240 | lld:lifeskim |
pubmed-article:2154620 | lifeskim:mentions | umls-concept:C0449450 | lld:lifeskim |
pubmed-article:2154620 | pubmed:issue | 3 | lld:pubmed |
pubmed-article:2154620 | pubmed:dateCreated | 1990-3-26 | lld:pubmed |
pubmed-article:2154620 | pubmed:abstractText | The ability of B cells, B blasts, and macrophages to present Epstein-Barr virion antigens to autologous T cells and trigger their capacity to inhibit Epstein-Barr virus-induced B-cell transformation was tested. Macrophages were as efficient as B cells and B blasts in presenting the virus to T lymphocytes. This function required antigen processing, because it was inhibited by chloroquine treatment and by fixation of the antigen-presenting cells immediately after viral exposure but not 18 h later. T cells exposed to the purified Epstein-Barr virus envelope antigen gp350 coupled to immunostimulating complexes also showed inhibitory function. These results suggest that recognition of processed virion antigens elicits the generation of T-cell-mediated inhibition of Epstein-Barr virus-induced B-cell transformation. | lld:pubmed |
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pubmed-article:2154620 | pubmed:language | eng | lld:pubmed |
pubmed-article:2154620 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2154620 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:2154620 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2154620 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:2154620 | pubmed:month | Mar | lld:pubmed |
pubmed-article:2154620 | pubmed:issn | 0022-538X | lld:pubmed |
pubmed-article:2154620 | pubmed:author | pubmed-author:KleinGG | lld:pubmed |
pubmed-article:2154620 | pubmed:author | pubmed-author:MorganAA | lld:pubmed |
pubmed-article:2154620 | pubmed:author | pubmed-author:MoreinBB | lld:pubmed |
pubmed-article:2154620 | pubmed:author | pubmed-author:KleinEE | lld:pubmed |
pubmed-article:2154620 | pubmed:author | pubmed-author:MasucciM GMG | lld:pubmed |
pubmed-article:2154620 | pubmed:author | pubmed-author:BejaranoM TMT | lld:pubmed |
pubmed-article:2154620 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:2154620 | pubmed:volume | 64 | lld:pubmed |
pubmed-article:2154620 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:2154620 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:2154620 | pubmed:pagination | 1398-401 | lld:pubmed |
pubmed-article:2154620 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
pubmed-article:2154620 | pubmed:meshHeading | pubmed-meshheading:2154620-... | lld:pubmed |
pubmed-article:2154620 | pubmed:meshHeading | pubmed-meshheading:2154620-... | lld:pubmed |
pubmed-article:2154620 | pubmed:meshHeading | pubmed-meshheading:2154620-... | lld:pubmed |
pubmed-article:2154620 | pubmed:meshHeading | pubmed-meshheading:2154620-... | lld:pubmed |
pubmed-article:2154620 | pubmed:meshHeading | pubmed-meshheading:2154620-... | lld:pubmed |
pubmed-article:2154620 | pubmed:meshHeading | pubmed-meshheading:2154620-... | lld:pubmed |
pubmed-article:2154620 | pubmed:meshHeading | pubmed-meshheading:2154620-... | lld:pubmed |
pubmed-article:2154620 | pubmed:meshHeading | pubmed-meshheading:2154620-... | lld:pubmed |
pubmed-article:2154620 | pubmed:meshHeading | pubmed-meshheading:2154620-... | lld:pubmed |
pubmed-article:2154620 | pubmed:year | 1990 | lld:pubmed |
pubmed-article:2154620 | pubmed:articleTitle | Epstein-Barr virus (EBV) antigens processed and presented by B cells, B blasts, and macrophages trigger T-cell-mediated inhibition of EBV-induced B-cell transformation. | lld:pubmed |
pubmed-article:2154620 | pubmed:affiliation | Department of Tumor Biology, Karolinska Institutet, Stockholm, Sweden. | lld:pubmed |
pubmed-article:2154620 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:2154620 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
pubmed-article:2154620 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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