Epstein-Barr Virus and Human Disease 1987
DOI: 10.1007/978-1-4612-4590-2_89
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Differential Expression of EB-Viral and Cellular Surface Markers on Burkitt Lymphoma and Lymphoblastoid Cell Lines

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Cited by 4 publications
(2 citation statements)
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“…It has been shown that BL cells either do not produce LMP or at most in a truncated form [Modrow and Wolf, 1986]; in addition, certain peripheral blood cells have been identified, which do not ex press LMP. Furthermore, even in cell lines known to express LMP, only less than 10% of cells show a high level of LMP expression, the rest expresses LMP at most to a much lesser extent [Modrow and Wolf, 1986;Modrow et al, 1987], It has been shown by several groups that absence of LMP would allow such cells to escape specific killing [Jilg et al, 1988Thorley-Lawson and Israelsohn, 1987]. Other latent gene products are either absent or, in the case of EBNA1, have a high homology to a cel lular gene and are not targets for T-cell-mediated cell lysis.…”
Section: How Does the Immune System Control Ebv-infected Cells?mentioning
confidence: 99%
“…It has been shown that BL cells either do not produce LMP or at most in a truncated form [Modrow and Wolf, 1986]; in addition, certain peripheral blood cells have been identified, which do not ex press LMP. Furthermore, even in cell lines known to express LMP, only less than 10% of cells show a high level of LMP expression, the rest expresses LMP at most to a much lesser extent [Modrow and Wolf, 1986;Modrow et al, 1987], It has been shown by several groups that absence of LMP would allow such cells to escape specific killing [Jilg et al, 1988Thorley-Lawson and Israelsohn, 1987]. Other latent gene products are either absent or, in the case of EBNA1, have a high homology to a cel lular gene and are not targets for T-cell-mediated cell lysis.…”
Section: How Does the Immune System Control Ebv-infected Cells?mentioning
confidence: 99%
“…However, a more detailed study of such differences at the molecular level has only recently become possible. This was achieved by using panels of specific monoclonal antibodies , by studying differential sensitivity to MHC-restricted T-cell cytotoxicity Torsteinsdottir et al, 1986) or by performing direct qualitative and quantitative analysis of surface components coded either by the viral (LYDMA or BNLF 1-MA) or the cellular genomes (MHC-products) (Modrow and Wolf, 1986;Modrow et al, 1987).…”
mentioning
confidence: 99%