Epstein–Barr virus expression in Hodgkin’s disease in relation to patient characteristics, serum factors and blood lymphocyte function
Open Access
- 12 November 1999
- journal article
- research article
- Published by Springer Nature in British Journal of Cancer
- Vol. 81 (7) , 1182-1187
- https://doi.org/10.1038/sj.bjc.6690827
Abstract
Epstein–Barr virus (EBV) expression was investigated by immunohistochemistry (latent membrane protein 1 [LMP-1]) and in situ hybridization (EBV encoded RNA [EBER]) in biopsies from 95 patients with untreated Hodgkin’s disease (HD). Tumour EBV status was related to EBV antibody titres, spontaneous and concanavallin A induced blood lymphocyte DNA synthesis, serum levels of soluble (s) CD4, sCD8, sCD25, sCD30, sCD54, β2-microglobulin, thymidine-kinase, routine chemistry, patient characteristics, complete remission and survival. The median follow-up time was 145 months (range 60–257). Tumour EBV-positive (n = 30; 33%) and negative (n = 62; 67%) patients did not differ with regard to sex, age, stage, presence of bulky disease or B-symptoms, remission rate or survival. The proportion of EBV+ cases was significantly higher among patients with mixed cellularity histopathology (58%) as compared to the nodular sclerosis subtype (18%; P < 0.001). The total white blood cell (WBC) counts were significantly lower in EBV+ patients (P < 0.01), who also had significantly higher levels of sCD54 (P < 0.02) and a tendency towards lower levels of sCD30 (P = 0.056). Patients in the tumour EBV+ group had significantly higher IgG antibody titres to restricted early antigen (EA-R) (P < 0.02). Hence, clinical features and outcome were not related to tumour EBV status. However, HD patients with EBV+ tumours had elevated sCD54 levels, higher antibody titres to EA-R and decreased total WBC counts. A potential causal relationship between EBV tumour status and these findings needs to be further explored. © 1999 Cancer Research CampaignKeywords
This publication has 49 references indexed in Scilit:
- CD30 Ligand, a Member of the TNF Ligand Superfamily, with Growth and Activation Control for CD30+ Lymphoid and Lymphoma Cells*Leukemia & Lymphoma, 1996
- Evaluation of epstein-barr virus antibody patterns and detection of viral markers in the biopsies of patients with Hodgkin's diseaseInternational Journal of Cancer, 1994
- Epstein‐Barr virus and Hodgkin's disease: A comparative immunological, in situ hybridization, and polymerase chain reaction studyAPMIS, 1994
- Expression of EBV Encoded Latent Membrane Protein 1 (LMP-1) and bcl-2 Protein in Childhood and Adult Hodgkin's Disease: Application of Microwave Irradiation for Antigen RetrievalLeukemia & Lymphoma, 1994
- ICAM-1 tissue overexpression associated with increased serum levels of its soluble form in Hodgkin's diseaseBritish Journal of Haematology, 1993
- Influence of Epstein-Barr Virus Encoded Latent Membrane Protein 1 on the Expression of CD23 Antigen, ICAM-1 and LFA-3 in Hodgkin and Reed-Sternberg Cells. A Morphometric AnalysisLeukemia & Lymphoma, 1993
- Lymphocyte abnormalities predicting a poor prognosis in Hodgkin's disease. A long-term follow-upCancer, 1991
- Hodgkin's Disease and Epstein-Barr VirusNew England Journal of Medicine, 1989
- An EBV membrane protein expressed in immortalized lymphocytes transforms established rodent cellsCell, 1985
- Immunoenzymatic labeling of monoclonal antibodies using immune complexes of alkaline phosphatase and monoclonal anti-alkaline phosphatase (APAAP complexes).Journal of Histochemistry & Cytochemistry, 1984