Epstein-Barr virus (EBV) has been found in most cases of rare gastric
lymphoepithelioma-like carcinomas and a small but significant proporti
on of common gastric adenocarcinomas. The presence of EBV in gastric c
ancer has been detected by polymerase chain reaction and in-situ hybri
dization, the latter technique demonstrating EBV in every malignant ep
ithelial cell. The carcinoma cells express EBNA1 but not the other EBN
As or LMP1. A single fused terminal fragment of the EBV genome was det
ected in each of the EBNA1-expressing tumours suggesting that the viru
s-positive gastric carcinomas represent a clonal proliferation of EBV-
infected cells. EBV antibody titres were elevated in patients with vir
us-positive carcinomas and also in those destined to develop EBV-posit
ive carcinomas. EBV-specific cytotoxic T-lymphocyte activity was retai
ned in patients with EBV-positive carcinomas suggesting that the tumou
rs can evade immunosurveillance possibly by only expressing the EBNA1
protein which is not able to be processed and presented. These results
implicate EBV as one of the factors contributing to the development o
f gastric cancer.