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Heterogeneity of HLA and EBER expression in epstein‐barr virus‐associated nasopharyngeal carcinoma
Author(s) -
Yao Yunhong,
Minter Helena A.,
Chen Xiaoyi,
Reynolds Gary M.,
Bromley Michael,
Arrand John R.
Publication year - 2000
Publication title -
international journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.475
H-Index - 234
eISSN - 1097-0215
pISSN - 0020-7136
DOI - 10.1002/1097-0215(20001215)88:6<949::aid-ijc18>3.0.co;2-6
Subject(s) - nasopharyngeal carcinoma , human leukocyte antigen , epstein–barr virus , biology , virus , immunology , immune system , phenotype , carcinoma , cancer research , antigen , gene , medicine , genetics , radiation therapy
Nasopharyngeal carcinoma (NPC) is an aggressive tumour of multifactorial aetiology that, although rare in most parts of the world, poses a significant mortality problem in its high incidence area of Southern China. Improved therapies are an urgent requirement and, towards this end, immunotherapeutic methods are being developed in several centres. Such strategies are dependent on the immune competence of the target tumour, in particular its expression of HLA class‐I. We examined HLA class‐I and ‐II expression in 27 primary NPC biopsies and found that 15% were extensively down‐regulated for class‐I expression with the majority of tumour cells appearing negative. Whilst HLA class‐II was expressed at high levels in the majority of tumours, 37% showed substantial down‐regulation. NPC is associated with Epstein‐Barr virus (EBV). Expression of the virus‐encoded EBER RNAs is accepted as a marker of EBV latency and is regarded as a valuable diagnostic criterion. EBER RNAs were expressed in all samples, but in some the level was remarkably heterogeneous, being barely detectable in many tumour cells. Our study reinforces the concept of extensive phenotypic variation in NPC. There are morphological differences between tumour cells. Some tumours express HLA class‐I and/or –II, whilst others are down‐regulated or negative. Individual tumours may or may not express the EBV‐encoded LMP‐1 protein, and individual tumour cells may express high levels of EBER, yet adjacent tumour cells express very little or none. Int. J. Cancer 88:949–955, 2000. © 2000 Wiley‐Liss, Inc.