7
views
0
recommends
+1 Recommend
1 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

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

      research-article

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          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.

          Related collections

          Most cited references25

          • Record: found
          • Abstract: not found
          • Article: not found

          Classification of leprosy according to immunity. A five-group system.

            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Mycobacterium tuberculosis prevents inflammasome activation.

            Mycobacterium tuberculosis (Mtb) parasitizes host macrophages and subverts host innate and adaptive immunity. Several cytokines elicited by Mtb are mediators of mycobacterial clearance or are involved in tuberculosis pathology. Surprisingly, interleukin-1beta (IL-1beta), a major proinflammatory cytokine, has not been implicated in host-Mtb interactions. IL-1beta is activated by processing upon assembly of the inflammasome, a specialized inflammatory caspase-activating protein complex. Here, we show that Mtb prevents inflammasome activation and IL-1beta processing. An Mtb gene, zmp1, which encodes a putative Zn(2+) metalloprotease, is required for this process. Infection of macrophages with zmp1-deleted Mtb triggered activation of the inflammasome, resulting in increased IL-1beta secretion, enhanced maturation of Mtb containing phagosomes, improved mycobacterial clearance by macrophages, and lower bacterial burden in the lungs of aerosol-infected mice. Thus, we uncovered a previously masked role for IL-1beta in the control of Mtb and a mycobacterial system that prevents inflammasome and, therefore, IL-1beta activation.
              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              Classification of leprosy according to immunity A five-group system

                Bookmark

                Author and article information

                Journal
                Mem Inst Oswaldo Cruz
                Mem. Inst. Oswaldo Cruz
                mioc
                Memórias do Instituto Oswaldo Cruz
                Instituto Oswaldo Cruz, Ministério da Saúde
                0074-0276
                1678-8060
                27 February 2020
                2020
                : 115
                : e190324
                Affiliations
                [1 ]Universidade Federal de Minas Gerais, Faculdade de Medicina, Departamento de Anatomia Patológica e Medicina Legal, Belo Horizonte, MG, Brasil
                [2 ]Universidade Federal de Minas Gerais, Faculdade de Medicina, Departamento de Clínica Médica, Belo Horizonte, MG, Brasil
                [3 ]Fundação Oswaldo Cruz-Fiocruz, Instituto René Rachou, Belo Horizonte, MG, Brasil
                Author notes
                + Corresponding author: mpascoal@ 123456medicina.ufmg.br

                AUTHORS’ CONTRIBUTION: ALGM - Immunohistochemical experiments and analyses and writing of the article; HDMJ, MISZ, RMA, JRMP and MMGA - selection of participants and immunohistochemistry experiments; ACMG, EJO and VPM - scientific discussion and elaboration of analysis strategies; MAPX - scientific discussion, elaboration of analysis strategies, immunohistochemical analyses and writing of the article. The authors declare that the poster of the study was presented at the XXXI Brazilian Congress of Pathology and Mucosal Immuno 2017. The authors do not have a commercial or other association that might pose a conflict of interest.

                Author information
                http://orcid.org/0000-0002-9081-1493
                Article
                00303
                10.1590/0074-02760190324
                7046136
                32130367
                9f537653-7935-4b78-8ca4-cd8f22437f9f

                This is an open-access article distributed under the terms of the Creative Commons Attribution License

                History
                : 28 August 2019
                : 22 January 2020
                Page count
                Figures: 2, Tables: 2, References: 26
                Categories
                Original Article

                leprosy,inflammasome,nlrp3,caspase
                leprosy, inflammasome, nlrp3, caspase

                Comments

                Comment on this article