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作 者:Natasha Kamal Beatriz Marciano Bryan Curtin Anna Strongin Suk See DeRavin Athos Bousvaros Christopher Koh Harry L.Malech Steven M.Holland Christa Zerbe Theo Heller
机构地区:[1]Digestive Disease Branch,National Institute of Diabetes and Digestive and Kidney Diseases,National Institutes of Health,Bethesda,MD,USA [2]Laboratory of Host Defenses,National Institute of Allergy and Infectious Diseases,National Institutes of Health,Bethesda,MD,USA [3]Division of Gastroenterology,Hepatology and Nutrition,Boston Children’s Hospital,Boston,MA,USA [4]Liver Disease Branch,National Institute of Diabetes and Digestive and Kidney Diseases,National Institutes of Health,Bethesda,MD,USA [5]Laboratory of Clinical Immunology and Microbiology,National Institute of Allergy and Infectious Diseases,National Institutes of Health,Bethesda,MD,USA
出 处:《Gastroenterology Report》2020年第5期404-406,I0003,共4页胃肠病学报道(英文)
基 金:This work was supported by intramural program at the National Institutes of Health.
摘 要:Introduction Chronic granulomatous disease(CGD)is a rare immunodeficiency affecting approximately 1 in 200,000 people[1].Patients with CGD are unable to produce normal amounts of neutrophil superoxide and other phagocyte reactive oxygen species.As a result,phagocytes have decreased microbicidal activity and patients develop recurrent bacterial and fungal infections.
关 键 词:慢性肉芽肿 单抗治疗 炎症性肠病 IMMUNODEFICIENCY
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