Pauci- and Multibacillary Leprosy: Two Distinct, Genetically Neglected Diseases

PLoS Negl Trop Dis. 2016 May 24;10(5):e0004345. doi: 10.1371/journal.pntd.0004345. eCollection 2016 May.

Abstract

After sustained exposure to Mycobacterium leprae, only a subset of exposed individuals develops clinical leprosy. Moreover, leprosy patients show a wide spectrum of clinical manifestations that extend from the paucibacillary (PB) to the multibacillary (MB) form of the disease. This "polarization" of leprosy has long been a major focus of investigation for immunologists because of the different immune response in these two forms. But while leprosy per se has been shown to be under tight human genetic control, few epidemiological or genetic studies have focused on leprosy subtypes. Using PubMed, we collected available data in English on the epidemiology of leprosy polarization and the possible role of human genetics in its pathophysiology until September 2015. At the genetic level, we assembled a list of 28 genes from the literature that are associated with leprosy subtypes or implicated in the polarization process. Our bibliographical search revealed that improved study designs are needed to identify genes associated with leprosy polarization. Future investigations should not be restricted to a subanalysis of leprosy per se studies but should instead contrast MB to PB individuals. We show the latter approach to be the most powerful design for the identification of genetic polarization determinants. Finally, we bring to light the important resource represented by the nine-banded armadillo model, a unique animal model for leprosy.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Alleles
  • Animals
  • Armadillos* / microbiology
  • Disease Models, Animal
  • Female
  • Genetic Variation
  • Genome-Wide Association Study
  • Humans
  • Leprosy, Multibacillary / epidemiology
  • Leprosy, Multibacillary / genetics*
  • Leprosy, Multibacillary / microbiology
  • Leprosy, Multibacillary / physiopathology
  • Leprosy, Paucibacillary / epidemiology
  • Leprosy, Paucibacillary / genetics*
  • Leprosy, Paucibacillary / microbiology
  • Leprosy, Paucibacillary / physiopathology
  • Male
  • Mycobacterium leprae / physiology
  • Neglected Diseases / epidemiology
  • Neglected Diseases / genetics*
  • Neglected Diseases / microbiology

Grants and funding

JG is funded by Fondation pour la Recherche Medicale. This work was supported by the Programme Blanc de l’Agence National de la Recherche, the Programme MALTALEP de l’Ordre de Malte, and by the Canadian Institutes of Health Research (CIHR). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.