Frequent expression of interleukin-10 by Epstein-Barr virus-harboring tumor cells of Hodgkin's disease

被引:155
作者
Herbst, H
Foss, HD
Samol, J
Araujo, I
Klotzbach, H
Krause, H
Agathanggelou, A
Niedobitek, G
Stein, H
机构
[1] FREE UNIV BERLIN,INST PATHOL,KONSULTAT & REFERENZZENTRUM LYMPHKNOTEN & HAMATOP,W-1000 BERLIN,GERMANY
[2] FREE UNIV BERLIN,KLINIKUM BENJAMIN FRANKLIN,INST IMMUNOL,W-1000 BERLIN,GERMANY
[3] UNIV BIRMINGHAM,DEPT PATHOL,BIRMINGHAM,W MIDLANDS,ENGLAND
关键词
D O I
10.1182/blood.V87.7.2918.bloodjournal8772918
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Tumor cells of Epstein-Barr virus (EBV)-associated Hodgkin's disease (HD) express the viral protein, latent infection membrane protein-1 (LMP1), but evade cytotoxic responses normally directed at this antigen. We tested whether local production of the immunoregulatory interleukins (IL)-4 and -10 may have a role in this process. IL-4 RNA was not detectable in any of the HD cases. By contrast, isotopic in situ hybridization and correlation with the presence of EBV gene products showed significantly higher proportions of cases with IL-10 expressing tumor cells in LMP1-positive (17 of 26, 66%) as compared with LMP1-negative HD cases (six of 37, 16%). Absence of EBV BCRF1 RNA indicated that the transcripts originated from the cellular IL-10 gene. Similarly, an association between IL-10 expression and EBV-infection of tumor cells was found in AIDS-related malignant non-Hodgkin lymphomas (ARL). Very small proportions of EBV-infected cells, mainly blasts, expressed IL-10 in infectious mononucleosis tonsils, Thus, although not entirely exclusive to EBV-positive cases, IL-10 expression is frequently associated with EBV-infection in HD and ARL and appears to be upregulated by EBV, most likely through LMP1. In view of the established inhibitory effects of IL-10 on cell mediated immunity, it is suggested that IL-10 expression may contribute to evasion of LMP1-positive cells from cytotoxicity directed at viral antigens. (C) 1996 by The American Society of Hematology.
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页码:2918 / 2929
页数:12
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