Expression of NLRP3 inflammasome in leprosy indicates immune evasion of Mycobacterium leprae

Mem Inst Oswaldo Cruz. 2020 Feb 27:115:e190324. doi: 10.1590/0074-02760190324. eCollection 2020.

Abstract

Background: Leprosy is an infectious-contagious disease caused by Mycobacterium leprae that remain endemic in 105 countries. This neglected disease has a wide range of clinical and histopathological manifestations that are related to the host inflammatory and immune responses. More recently, the inflammasome has assumed a relevant role in the inflammatory response against microbiological agents. However, the involvement of inflammasome in leprosy remains poorly understood.

Objectives: The aim is to associate biomarkers of inflammasome with the different immunopathological forms of leprosy.

Methods: We performed an observational, cross-sectional, and comparative study of the immunophenotypic expression of inflammasome-associated proteins in immunopathological forms of leprosy of 99 skin lesion samples by immunohistochemistry. The intensity and percentage of NLRP3, Caspase-1, Caspases-4/5, interleukin-1β and interleukin-18 immunoreactivities in the inflammatory infiltrate of skin biopsies were evaluated.

Findings: Strong expression of NLRP3 and inflammatory Caspases-4/5 were observed in lepromatous leprosy (lepromatous pole). In addition, were observed low expression of caspase-1, interleukin-1β, and interleukin-18 in tuberculoid and lepromatous leprosy. The interpolar or borderline form showed immunophenotype predominantly similar to the lepromatous pole.

Main conclusions: Our results demonstrate that the NLRP3 inflammasome is inactive in leprosy, suggesting immune evasion of M. leprae.

Publication types

  • Comparative Study
  • Observational Study

MeSH terms

  • Cross-Sectional Studies
  • Humans
  • Immune Evasion / immunology*
  • Immunohistochemistry
  • Inflammasomes / metabolism*
  • Leprosy / immunology*
  • Leprosy / metabolism*
  • Leprosy / pathology
  • Mycobacterium leprae / immunology*
  • NLR Family, Pyrin Domain-Containing 3 Protein / metabolism*

Substances

  • Inflammasomes
  • NLR Family, Pyrin Domain-Containing 3 Protein