Differential expression of viral and human interleukin-10 (IL-10) by primary B cell tumors and B cell lines.
dc.contributor.author | Stewart, James P | |
dc.contributor.author | Behm, F G | |
dc.contributor.author | Arrand, John R | |
dc.contributor.author | Rooney, Claire M | |
dc.date.accessioned | 2010-04-09T13:51:11Z | |
dc.date.available | 2010-04-09T13:51:11Z | |
dc.date.issued | 1994-05-01 | |
dc.identifier.citation | Differential expression of viral and human interleukin-10 (IL-10) by primary B cell tumors and B cell lines. 1994, 200 (2):724-32 Virology | en |
dc.identifier.issn | 0042-6822 | |
dc.identifier.pmid | 8178456 | |
dc.identifier.doi | 10.1006/viro.1994.1236 | |
dc.identifier.uri | http://hdl.handle.net/10541/96186 | |
dc.description.abstract | Human and viral interleukin-10 (IL-10) possess growth factor activity for human B cells and may act as autocrine growth factors in B cell malignancies. To study this possibility we have measured viral (v) and human (h) IL-10 expression in EBV-positive and negative B lineage tumors and tumor cell lines. Previous studies demonstrated IL-10 expression in cell lines and now we describe the pattern of IL-10 expression in primary Burkitt's lymphoma (BL) tumor biopsies and in BL lines of defined phenotypes. vIL-10 was expressed during the lytic (productive) phase of EBV infection, but not during virus latency. Although hIL-10 was expressed in the majority of B cell lines, it was not expressed in two BL biopsy specimens. Expression of hIL-10 did not correlate with the presence of EBV, but was associated with the differentiation state of the B cell line. Thus, vIL-10 may enhance the persistence of B cells infected at sites of virus replication, and while hIL-10 may be a factor in the growth both in vivo and in vitro of some BLs and EBV-transformed B cells, it is not an absolute requirement. | |
dc.language.iso | en | en |
dc.subject.mesh | B-Lymphocytes | |
dc.subject.mesh | Base Sequence | |
dc.subject.mesh | Biopsy | |
dc.subject.mesh | Burkitt Lymphoma | |
dc.subject.mesh | Cell Differentiation | |
dc.subject.mesh | Cell Line | |
dc.subject.mesh | DNA Probes | |
dc.subject.mesh | Herpesvirus 4, Human | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Interleukin-10 | |
dc.subject.mesh | Models, Biological | |
dc.subject.mesh | Molecular Sequence Data | |
dc.subject.mesh | Viral Proteins | |
dc.subject.mesh | Virus Latency | |
dc.title | Differential expression of viral and human interleukin-10 (IL-10) by primary B cell tumors and B cell lines. | en |
dc.type | Article | en |
dc.contributor.department | Department of Virology and Molecular Biology, St. Jude Children's Research Hospital, Memphis, Tennessee 38101-0318. | en |
dc.identifier.journal | Virology | en |
html.description.abstract | Human and viral interleukin-10 (IL-10) possess growth factor activity for human B cells and may act as autocrine growth factors in B cell malignancies. To study this possibility we have measured viral (v) and human (h) IL-10 expression in EBV-positive and negative B lineage tumors and tumor cell lines. Previous studies demonstrated IL-10 expression in cell lines and now we describe the pattern of IL-10 expression in primary Burkitt's lymphoma (BL) tumor biopsies and in BL lines of defined phenotypes. vIL-10 was expressed during the lytic (productive) phase of EBV infection, but not during virus latency. Although hIL-10 was expressed in the majority of B cell lines, it was not expressed in two BL biopsy specimens. Expression of hIL-10 did not correlate with the presence of EBV, but was associated with the differentiation state of the B cell line. Thus, vIL-10 may enhance the persistence of B cells infected at sites of virus replication, and while hIL-10 may be a factor in the growth both in vivo and in vitro of some BLs and EBV-transformed B cells, it is not an absolute requirement. |