肺结核
结核分枝杆菌
免疫学
结合珠蛋白
遗传倾向
血色病
巨噬细胞
医学
缺铁
铁状态
表型
风险因素
川地163
铁转运蛋白
炎症
贫血
生物
内科学
海西定
遗传学
病理
疾病
基因
体外
作者
Johan R. Boelaert,Stefaan J. Vandecasteele,Rui Appelberg,Victor R. Gordeuk
摘要
Several lines of evidence have suggested that iron is critical for Mycobacterium tuberculosis growth in macrophages. Macrophage iron loading in patients with African iron overload increases the risk of tuberculosis (TB) and may worsen TB outcome. Likewise, macrophage iron loading may contribute to an increased predisposition toward TB in HIV infection. Human genetic disorders or variations may increase the risk of TB or worsen its outcome through macrophage iron loading, including the haptoglobin 2-2 phenotype, NRAMP1 polymorphisms (at least in Africans and Asians), and possibly ferroportin 1 mutations, but not HFE hemochromatosis. Thus, the host's iron status may be an important yet underevaluated factor in TB prevention and therapy and in TB vaccine design.
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