TY - JOUR KW - Communicable Diseases KW - Crohn Disease KW - Genetic Markers KW - Genetic Predisposition to Disease KW - Genome-Wide Association Study KW - Humans KW - Inflammation KW - leprosy KW - Mycobacterium leprae AU - Gaschignard J AU - Scurr E AU - Alcaïs A AB -
Despite a natural reservoir of Mycobacterium leprae limited to humans and free availability of an effective antibiotic treatment, more than 200,000 people develop leprosy each year. This disease remains a major cause of disability and social stigma worldwide. The cause of this constant incidence is currently unknown and indicates that important aspects of the complex relationship between the pathogen and its human host remain to be discovered. An important contribution of host genetics to susceptibility to leprosy has long been suggested to account for the considerable variability between individuals sustainably exposed to M. leprae. Given the inability to cultivate M. leprae in vitro and in the absence of relevant animal model, genetic epidemiology is the main strategy used to identify the genes and, consequently, the immunological pathways involved in protective immunity to M. leprae. Recent genome-wide studies have identified new pathophysiological pathways which importance is only beginning to be understood. In addition, the prism of human genetics placed leprosy at the crossroads of other common diseases such as Crohn's disease, asthma or myocardial infarction. Therefore, novel lights on the pathogenesis of many common diseases could eventually emerge from the detailed understanding of a disease of the shadows.
BT - Pathologie-biologie C1 - http://www.ncbi.nlm.nih.gov/pubmed/23711949?dopt=Abstract CN - GASCHIGNARD 2014 DA - 2013 Jun DO - 10.1016/j.patbio.2013.03.003 IS - 3 J2 - Pathol. Biol. LA - fre N2 -Despite a natural reservoir of Mycobacterium leprae limited to humans and free availability of an effective antibiotic treatment, more than 200,000 people develop leprosy each year. This disease remains a major cause of disability and social stigma worldwide. The cause of this constant incidence is currently unknown and indicates that important aspects of the complex relationship between the pathogen and its human host remain to be discovered. An important contribution of host genetics to susceptibility to leprosy has long been suggested to account for the considerable variability between individuals sustainably exposed to M. leprae. Given the inability to cultivate M. leprae in vitro and in the absence of relevant animal model, genetic epidemiology is the main strategy used to identify the genes and, consequently, the immunological pathways involved in protective immunity to M. leprae. Recent genome-wide studies have identified new pathophysiological pathways which importance is only beginning to be understood. In addition, the prism of human genetics placed leprosy at the crossroads of other common diseases such as Crohn's disease, asthma or myocardial infarction. Therefore, novel lights on the pathogenesis of many common diseases could eventually emerge from the detailed understanding of a disease of the shadows.
PY - 2013 SP - 120 EP - 8 T2 - Pathologie-biologie TI - [Leprosy, a pillar of human genetics of infectious diseases]. TT - La lèpre, pilier de la génétique des maladies infectieuses VL - 61 SN - 1768-3114 ER -