2009
DOI: 10.1111/j.1751-2980.2009.00395.x
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Association of the human leukocyte antigen class II alleles with chronic atrophic gastritis and gastric carcinoma in Koreans

Abstract: OBJECTIVE:Gastric carcinogenesis is a multi-step process and is influenced by several etiological agents, including the host's genetic factors. Since whether a patient remains with chronic superficial gastritis (CSG) or progresses to either chronic atrophic gastritis (CAG) or gastric carcinoma (GC) could be a genetic predisposition unique in each population, we hypothesized that host human leukocyte antigen (HLA) alleles could be discriminative in predicting the risk of CSG progression to precancerous CAG and … Show more

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Cited by 28 publications
(23 citation statements)
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“…28,29 Moreover, different HLA alleles may be contribute to development and progression of gastric cancer in the diverse ethnic groups. 27 …”
Section: Discussionmentioning
confidence: 97%
See 1 more Smart Citation
“…28,29 Moreover, different HLA alleles may be contribute to development and progression of gastric cancer in the diverse ethnic groups. 27 …”
Section: Discussionmentioning
confidence: 97%
“…The distribution of HLA alleles and the linkage disequilibrium among alleles from diverse HLA gene differ in various ethnic populations. 26,27 In addition, relatively small populations were included in several studies. Third, the different antibody, immunostaining method, and scoring system may have contributed to discrepancies.…”
Section: Discussionmentioning
confidence: 99%
“…Recent studies have supported the hypothesis that genetic predisposition associated with human leukocyte antigen (HLA) genes have a role in the development of gastric cancer. In H. pylori-positive gastric cancers, studies especially conducted on class II HLA-DRB1* and HLA-DQB1* antigens attract attention (5,7) . To our knowledge, there are no studies on tissue groups in H. pylori-positive pediatric patients with active gastritis and duodenal ulcer in Turkish population.…”
Section: Introductionmentioning
confidence: 99%
“…The HpaA88-100 specific CD4 + T cell response was found to be associated with resistance to severe gastric diseases correlated to H. pylori infection in HLA-DRB1*1501 positive subjects [20]. A negative association with HLA-DRB1*1501 allele, reported in H. pylori -positive patients with gastric ulcers when compared with uninfected healthy controls, further supported this potential protective role mediated by HLA-DRB1*1501 restricted HpaA88-100 specific CD4 + T cell response [30, 31]. Here, we demonstrated that it was not the broad of peptide specificity, but the strength of HpaA specific CD4 + T cell responses was associated with gastric diseases potentially caused by H. pylori infection (Figure 5).…”
Section: Discussionmentioning
confidence: 97%