Epstein-Barr virus infection and risk of lymphoma: Immunoblot analysis of antibody responses against EBV-related proteins in a large series of lymphoma subjects and matched controls

被引:40
作者
de Sanjose, Silvia
Bosch, Ramon
Schouten, Tabitha
Verkuijlen, Sandra
Nieters, Alexandra
Foretova, Lenka
Maynadie, Marc
Cocco, Pier Luigi
Staines, Anthony
Becker, Nikolaus
Brennan, Paul
Benavente, Yolanda
Boffetta, Paolo
Meijer, Chris J. L. M.
Middeldorp, Jaap M.
机构
[1] Catalan Inst Oncol, Barcelona, Spain
[2] Hosp Verge Cinta, Dept Pathol, Tortosa, Spain
[3] Univ Hosp Vrije, Dept Pathol, Amsterdam, Netherlands
[4] German Canc Res Ctr, D-6900 Heidelberg, Germany
[5] Masaryk Mem Canc Ins, Brno, Czech Republic
[6] Registre Hemopathies Malignes Cote Dor, Dijon, France
[7] Univ Cagliari, Inst Occupat Med, Cagliari, Italy
[8] Publ Hlth Univ Coll, Dublin, Ireland
[9] Int Agcy Res Canc, F-69372 Lyon, France
关键词
Epstein Barr virus; lymphoma; case control; leukaemia;
D O I
10.1002/ijc.22857
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Epstein-Barr Virus (EBV) is consistently associated with distinct lymphoproliferative malignancies and aberrant EBV antibody patterns are found in most EBV cancer patients. We evaluate the detection of an abnormal reactive serological pattern to EBV (ab_EBV) infection and the risk of lymphoma in a multicentric case-control study. Serum samples were collected at study entry from 1,085 incident lymphoma cases from Spain, France, Germany, Czech Republic, Italy and 1,153 age, sex and country matched controls. EBV immunoglobulin G (IgG) serostatus was evaluated through a peptide-based ELISA combining immunodominant epitopes of EBNA1 (BKRF1) and VCA-p18 (BFRF3). Further, immunoblot analysis was performed to evaluate distinct antibody diversity patterns to EBV early antigens (EA), besides EBNA1, VCA-p18, VCA-p40 (BdRF1) and Zebra (BZLF1). Patients with chronic active EBV infection and aberrant EBV activity were characterized as having an abnormal reactive pattern (ab_EBV). Ab EBV was observed in 20.9% of 2,238 included subjects with an increased proportion of cases presenting ab_EBV as compared to the control population (23.9% vs. 18.0% p = 0.001). Ab_EBV positivity was a risk factor for all lymphomas combined (odds ratio [OR] = 1.42, 95% confidence interval [CI]=1.15-1.74), and specifically for chronic lymphocytic leukaemia (OR = 2.96, 95%CI = 2.22-3.95). Lower levels of ab EBV were observed for follicular lymphoma (OR = 0.38, 95%-CI = 0.15-0.98). EBV may be involved in a larger subset of lymphomas among clinically immunocompetent subjects than previously thought, probably explained by an underlying loss of immune control of EBV latent infection. Ab_EBV is a useful too] to explore EBV imbalances preceeding or paralleling possible EBV associated oncogenic events. (C) 2007 Wiley-Liss, Inc.
引用
收藏
页码:1806 / 1812
页数:7
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