Differential mast cell numbers and characteristics in human tuberculosis pulmonary lesions

Abstract Tuberculosis (TB) is still a major worldwide health threat and primarily a lung disease. The innate immune response against Mycobacterium tuberculosis (Mtb) is orchestrated by dendritic cells, macrophages, neutrophils, natural killer cells and apparently mast cells (MCs). MCs are located at...

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Main Authors: Karen Magdalena Garcia-Rodriguez, Estela Isabel Bini, Armando Gamboa-Domínguez, Clara Inés Espitia-Pinzón, Sara Huerta-Yepez, Silvia Bulfone-Paus, Rogelio Hernández-Pando
Format: Article
Language:English
Published: Nature Publishing Group 2021-05-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-89659-6
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spelling doaj-c2a45d9a534d4e06a1b51636fd77f89a2021-05-23T11:33:54ZengNature Publishing GroupScientific Reports2045-23222021-05-011111910.1038/s41598-021-89659-6Differential mast cell numbers and characteristics in human tuberculosis pulmonary lesionsKaren Magdalena Garcia-Rodriguez0Estela Isabel Bini1Armando Gamboa-Domínguez2Clara Inés Espitia-Pinzón3Sara Huerta-Yepez4Silvia Bulfone-Paus5Rogelio Hernández-Pando6Lydia Becker Institute of Immunology and Inflammation, Faculty of Biology, Medicine and Health, University of ManchesterSeccion de Patologia Experimental, Instituto Nacional de Ciencias Medicas y Nutricion “Salvador Zubiran”Seccion de Patologia Experimental, Instituto Nacional de Ciencias Medicas y Nutricion “Salvador Zubiran”Departamento de Inmunologia, Instituto de Investigaciones Biomedicas, Universidad Nacional Autonoma de MexicoUnidad de Investigacion en Enfermedades Oncologicas, Hospital Infantil de Mexico, Federico GomezLydia Becker Institute of Immunology and Inflammation, Faculty of Biology, Medicine and Health, University of ManchesterSeccion de Patologia Experimental, Instituto Nacional de Ciencias Medicas y Nutricion “Salvador Zubiran”Abstract Tuberculosis (TB) is still a major worldwide health threat and primarily a lung disease. The innate immune response against Mycobacterium tuberculosis (Mtb) is orchestrated by dendritic cells, macrophages, neutrophils, natural killer cells and apparently mast cells (MCs). MCs are located at mucosal sites including the lungs and contribute in host-defence against pathogens, but little is known about their role during Mtb infection. This study investigates the location and characteristics of MCs in TB lesions to assess their contribution to TB pathology. To this purpose, number, location and phenotype of MCs was studied in 11 necropsies of pulmonary TB and 3 necropsies of non-TB infected lungs that were used as controls. MCs were localised at pneumonic areas, in the granuloma periphery and particularly abundant in fibrotic tissue. Furthermore, MCs displayed intracellular Mtb and IL-17A and TGF-β immunostaining. These findings were validated by analysing, post-mortem lung tissue microarrays from 44 individuals with pulmonary TB and 25 control subjects. In affected lungs, increased numbers of MCs expressing intracellularly both tryptase and chymase were found at fibrotic sites. Altogether, our data suggest that MCs are recruited at the inflammatory site and that actively produce immune mediators such as proteases and TGF-β that may be contributing to late fibrosis in TB lesions.https://doi.org/10.1038/s41598-021-89659-6
collection DOAJ
language English
format Article
sources DOAJ
author Karen Magdalena Garcia-Rodriguez
Estela Isabel Bini
Armando Gamboa-Domínguez
Clara Inés Espitia-Pinzón
Sara Huerta-Yepez
Silvia Bulfone-Paus
Rogelio Hernández-Pando
spellingShingle Karen Magdalena Garcia-Rodriguez
Estela Isabel Bini
Armando Gamboa-Domínguez
Clara Inés Espitia-Pinzón
Sara Huerta-Yepez
Silvia Bulfone-Paus
Rogelio Hernández-Pando
Differential mast cell numbers and characteristics in human tuberculosis pulmonary lesions
Scientific Reports
author_facet Karen Magdalena Garcia-Rodriguez
Estela Isabel Bini
Armando Gamboa-Domínguez
Clara Inés Espitia-Pinzón
Sara Huerta-Yepez
Silvia Bulfone-Paus
Rogelio Hernández-Pando
author_sort Karen Magdalena Garcia-Rodriguez
title Differential mast cell numbers and characteristics in human tuberculosis pulmonary lesions
title_short Differential mast cell numbers and characteristics in human tuberculosis pulmonary lesions
title_full Differential mast cell numbers and characteristics in human tuberculosis pulmonary lesions
title_fullStr Differential mast cell numbers and characteristics in human tuberculosis pulmonary lesions
title_full_unstemmed Differential mast cell numbers and characteristics in human tuberculosis pulmonary lesions
title_sort differential mast cell numbers and characteristics in human tuberculosis pulmonary lesions
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2021-05-01
description Abstract Tuberculosis (TB) is still a major worldwide health threat and primarily a lung disease. The innate immune response against Mycobacterium tuberculosis (Mtb) is orchestrated by dendritic cells, macrophages, neutrophils, natural killer cells and apparently mast cells (MCs). MCs are located at mucosal sites including the lungs and contribute in host-defence against pathogens, but little is known about their role during Mtb infection. This study investigates the location and characteristics of MCs in TB lesions to assess their contribution to TB pathology. To this purpose, number, location and phenotype of MCs was studied in 11 necropsies of pulmonary TB and 3 necropsies of non-TB infected lungs that were used as controls. MCs were localised at pneumonic areas, in the granuloma periphery and particularly abundant in fibrotic tissue. Furthermore, MCs displayed intracellular Mtb and IL-17A and TGF-β immunostaining. These findings were validated by analysing, post-mortem lung tissue microarrays from 44 individuals with pulmonary TB and 25 control subjects. In affected lungs, increased numbers of MCs expressing intracellularly both tryptase and chymase were found at fibrotic sites. Altogether, our data suggest that MCs are recruited at the inflammatory site and that actively produce immune mediators such as proteases and TGF-β that may be contributing to late fibrosis in TB lesions.
url https://doi.org/10.1038/s41598-021-89659-6
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