Tumor Necrosis Factor–α and Interleukin-10 Promoter Polymorphisms in Epstein-Barr Virus–Associated Gastric Carcinoma

MS Wu, SP Huang, YT Chang, CT Shun… - The journal of …, 2002 - academic.oup.com
MS Wu, SP Huang, YT Chang, CT Shun, MC Chang, MT Lin, HP Wang, JT Lin
The journal of infectious diseases, 2002academic.oup.com
To investigate whether genetic differences in cytokine promoter polymorphisms effect
various outcomes after exposure to Epstein-Barr virus (EBV) infection, 30 patients with EBV-
positive gastric carcinoma (GC), 120 patients with EBV-negative GC, and 220 control
subjects were enrolled. Promoter polymorphisms of tumor necrosis factor (TNF)–α at
positions− 238 and− 308 and of interleukin (IL)–10 at position− 1082 were determined. The
frequency of the high-producer allele (− 308A) in the TNF-α gene was significantly higher …
Abstract
To investigate whether genetic differences in cytokine promoter polymorphisms effect various outcomes after exposure to Epstein-Barr virus (EBV) infection, 30 patients with EBV-positive gastric carcinoma (GC), 120 patients with EBV-negative GC, and 220 control subjects were enrolled. Promoter polymorphisms of tumor necrosis factor (TNF)–α at positions −238 and −308 and of interleukin (IL)–10 at position −1082 were determined. The frequency of the high-producer allele (−308A) in the TNF-α gene was significantly higher among EBV-positive GC patients compared with control subjects (23.3% vs. 12.0%, P<.05), whereas the frequency of the high-producer allele (−1082G) in the IL-10 gene was significantly higher among EBV-negative GC patients compared with control subjects (6.3% vs. 3.0%, P<.05). These data support the notion that genetic factors may modify the outcomes of infectious diseases through different TNF-α– or IL-10–producing capabilities
Oxford University Press