期刊论文详细信息
PLoS Pathogens
Role of ABO Secretor Status in Mucosal Innate Immunity and H. pylori Infection
Andre Dubois1  Cara Olsen2  Sara Lindén3  Ingemar Carlstedt3  Cristina Semino-Mora4  Thomas Borén5  Jafar Mahdavi5 
[1] Department of Preventive Medicine and Biometrics, Uniformed Services University of the Health Sciences, Bethesda, Maryland, United States of America;Division of Microbiology and Infectious Diseases, Queen's Medical Centre, Nottingham, United Kingdom;Laboratory of Gastrointestinal and Liver Studies, Digestive Diseases Division, Department of Medicine, Uniformed Services University of the Health Sciences, Bethesda, Maryland, United States of America;Mucosal Diseases Program, Mater Medical Research Institute, South Brisbane, Australia;United States Military Cancer Institute, Bethesda, Maryland, United States of America
关键词: Helicobacter pylori;    Gastrointestinal infections;    Monkeys;    Blood groups;    Inflammation;    Gastritis;    Mucin;    Epithelium;   
DOI  :  10.1371/journal.ppat.0040002
学科分类:生物科学(综合)
来源: Public Library of Science
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【 摘 要 】

The fucosylated ABH antigens, which constitute the molecular basis for the ABO blood group system, are also expressed in salivary secretions and gastrointestinal epithelia in individuals of positive secretor status; however, the biological function of the ABO blood group system is unknown. Gastric mucosa biopsies of 41 Rhesus monkeys originating from Southern Asia were analyzed by immunohistochemistry. A majority of these animals were found to be of blood group B and weak-secretor phenotype (i.e., expressing both Lewis a and Lewis b antigens), which are also common in South Asian human populations. A selected group of ten monkeys was inoculated with Helicobacter pylori and studied for changes in gastric mucosal glycosylation during a 10-month period. We observed a loss in mucosal fucosylation and concurrent induction and time-dependent dynamics in gastric mucosal sialylation (carbohydrate marker of inflammation), which affect H. pylori adhesion targets and thus modulate host–bacterial interactions. Of particular relevance, gastric mucosal density of H. pylori, gastritis, and sialylation were all higher in secretor individuals compared to weak-secretors, the latter being apparently “protected.” These results demonstrate that the secretor status plays an intrinsic role in resistance to H. pylori infection and suggest that the fucosylated secretor ABH antigens constitute interactive members of the human and primate mucosal innate immune system.

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