Alcaïs Alexandre, Mira Marcelo, Casanova Jean-Laurent, Schurr Erwin, Abel Laurent
Laboratoire de Génétique Humaine des Maladies Infectieuses, Université de Paris René Descartes, Institut National de la Santé et de la Recherche Medicale U.550, Faculté de Médecine Necker, Paris, France, European Union.
Curr Opin Immunol. 2005 Feb;17(1):44-8. doi: 10.1016/j.coi.2004.11.006.
Leprosy is a chronic infectious disease caused by Mycobacterium leprae that affects an estimated 700,000 new individuals each year. A strong contribution of host genetics to susceptibility to leprosy has long been suggested to account for the considerable variability observed between individuals exposed to M. leprae. As there is no relevant animal model for human leprosy, forward genetics is the main strategy used to identify the genes and, consequently, the immunological pathways involved in protective immunity to M. leprae. With respect to genome-wide screens, a major breakthrough has been reported this year; variants in the regulatory region shared by PARK2 and PACRG have been identified as being common risk factors for leprosy.
麻风病是一种由麻风分枝杆菌引起的慢性传染病,每年估计有70万新发病例。长期以来,人们一直认为宿主基因对麻风病易感性有很大影响,这可以解释在接触麻风分枝杆菌的个体之间观察到的显著差异。由于没有针对人类麻风病的相关动物模型,正向遗传学是用于识别基因以及因此识别参与对麻风分枝杆菌保护性免疫的免疫途径的主要策略。关于全基因组筛查,今年有一项重大突破;已确定PARK2和PACRG共享的调控区域中的变异是麻风病的常见风险因素。