Graduate Program in Health Sciences, School of Medicine, Pontifícia Universidade Católica do Paraná, Rua Imaculada Conceição 1155 - Prado Velho, Curitiba, Paraná, Brazil.
Tropical Medicine Centre, University of Brasília, UnB - Brasília, DF, Brazil.
Sci Rep. 2020 Jan 28;10(1):1284. doi: 10.1038/s41598-020-58079-3.
Host genetic susceptibility to leprosy has been intensively investigated over the last decades; however, there are no studies on the role of genetic variants in disease recurrence. A previous initiative identified three recurrent cases of leprosy for which none of the M. leprae strains, as obtained in the first and the second diagnosis, had any known genomic variants associated to resistance to Multidrug therapy; in addition, whole genome sequencing indicated that the same M. leprae was causing two out of the three recurrences. Thus, these individuals were suspected of being particularly susceptible to M. leprae infection, either as relapse or reinfection. To verify this hypothesis, 19 genetic markers distributed across 11 loci (14 genes) classically associated with leprosy were genotyped in the recurrent and in three matching non-recurrent leprosy cases. An enrichment of risk alleles was observed in the recurrent cases, suggesting the existence of a particularly high susceptibility genetic profile among leprosy patients predisposing to disease recurrence.
宿主对麻风病的遗传易感性在过去几十年中得到了深入研究;然而,目前还没有关于遗传变异在疾病复发中的作用的研究。先前的一项研究确定了三个麻风病复发病例,在首次和第二次诊断中获得的麻风分枝杆菌菌株均没有任何与耐多药治疗相关的已知基因组变异;此外,全基因组测序表明,相同的麻风分枝杆菌导致了其中两个复发病例。因此,这些人被怀疑对麻风分枝杆菌感染特别敏感,无论是复发还是再感染。为了验证这一假设,对 19 个遗传标记进行了基因分型,这些标记分布在 11 个位点(14 个基因)上,这些位点通常与麻风病有关,这些标记在复发和三个匹配的非复发麻风病病例中进行了基因分型。在复发病例中观察到风险等位基因的富集,这表明在麻风病患者中存在一种特别高的易感性遗传特征,容易导致疾病复发。