Genetic variations of EBV-LMP1 from nasopharyngeal carcinoma biopsies: potential loss of T cell epitopes

Brazilian Journal of Medical and Biological Research

Y.l. Tang¹  J.h. Lu¹  L. Cao¹  M.h. Wu¹  S.p. Peng¹  H.d. Zhou¹  C. Huang¹  Y.x. Yang¹  Y.h. Zhou¹  Q. Chen¹  X.l. Li¹  M. Zhou¹  G.y. Li¹ 

[1] ,Central South University Cancer Research Institute Changsha Hunan ,the People's Republic of China

关键词: Genetic variation;    Epitope;    Immune recognition;    Latent membrane protein 1;    Tumorigenicity;   

DOI  :  10.1590/S0100-879X2008000200006

来源: SciELO

【 摘 要 】

To find Epstein-Barr virus (EBV) strains with genetic variations of EBV latent membrane protein 1 (EBV-LMP1) from nasopharyngeal carcinoma (NPC), the full-length DNA of LMP1 genes from 21 NPC biopsies obtained in Hunan province in southern China was amplified and sequenced. Our sequences were compared to those previously reported by the Clustal V method. Results showed that all 21 sequences displayed two amino acid changes most frequently in LMP1 of CD4+ T cell epitopes at codons 144 (F®I, 21/21) and 212 (G®S, 19/21) or (G®N, 2/21). We also show that type A EBV strain is prevalent in the cases of NPC from Hunan province with a 30-bp 18/21 deletion, and we highlight that this deletion resulted in loss of one of the CD4+ T cell-restricted epitopes. The other 3 sequences without this deletion all had a change at codon 344 (G®D). Furthermore, in the major epitope sequence of CD8+ T cells restricted by HLA-A2, all 21 sequences showed changes at codons 126 (L®F) and 129 (M®I). Our study discovered that one of the 21 sequence variations harbored a new change at codon 131 (W®C), and 5/21 specimens showed another novel change at codon 115 (G®A) in the major epitope sequence of CD8+ T cells restricted by HLA-A2. Our study suggests that these sequence variations of NPC-derived LMP1 may lead to a potential escape from host cell immune recognition, protecting latent EBV infection and causing an increase in tumorigenicity.

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