EXPRESSION OF EPSTEIN-BARR VIRUS-ENCODED GROWTH-TRANSFORMATION-ASSOCIATED PROTEINS IN LYMPHOPROLIFERATIONS OF BONE-MARROW TRANSPLANT RECIPIENTS

被引:73
作者
GRATAMA, JW
ZUTTER, MM
MINAROVITS, J
OOSTERVEER, MAP
THOMAS, ED
KLEIN, G
ERNBERG, I
机构
[1] KAROLINSKA INST,DEPT TUMOR BIOL,S-10401 STOCKHOLM 60,SWEDEN
[2] STATE UNIV LEIDEN HOSP,DEPT IMMUNOHEMATOL,2333 AA LEIDEN,NETHERLANDS
[3] STATE UNIV LEIDEN HOSP,BLOOD BANK,2333 AA LEIDEN,NETHERLANDS
[4] WASHINGTON UNIV,SCH MED,DEPT PATHOL,ST LOUIS,MO 63110
[5] FRED HUTCHINSON CANC RES CTR,DIV CLIN RES,SEATTLE,WA 98104
关键词
D O I
10.1002/ijc.2910470205
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The expression of Epstein-Barr virus (EBV)-encoded, growth-transformation-associated proteins was studied in lymphoproliferations of 9 allogeneic bone-marrow transplant (BMT) recipients. Immunoblots of cell lysates were probed with polyspecific and monospecific antisera directed against EBNA 1, 2, 3 and 6, and the membrane protein LMP. All tumors expressed EBNA 1 and LMP. EBNA 2 was detected in the tumors of 8 patients, and EBNA 3 and 6 in the tumors of 5 patients. The LMP regulatory sequences, 5' of the LMP gene, were totally unmethylated in all 7 cases, while the coding sequences of LMP and EBNA 2 were more methylated in CpG dinucleotides. EBV-transformed lymphoblastoid cell lines (LCL) express EBNA 1 to 6 and LMP; in contrast, Burkitt lymphomas express only EBNA 1. In vitro experiments have shown that EBNA 2, 3 and LMP can generate targets for cytotoxic T cells (CTL). These combined observations are consistent with the hypothesis that the EBV-associated lymphoproliferative disease of the BMT recipients escapes CTL-mediated rejection due to the failure of host immunosurveillance rather than to the down-regulation of immunogenic EBV-encoded antigens.
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收藏
页码:188 / 192
页数:5
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