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Live Vaccines Have Different NK Cells and Neutrophils Requirements for the Development of a Protective Immune Response Against Tuberculosis
It has been shown that neutrophils drive NK cells to activate DCs while NK cells regulate neutrophils survival. In response to mycobacteria, NK cells proliferate and produces IFN-γ, that appears to regulate the neutrophilic inflammatory responses to both M. tuberculosis infection and BCG vaccination...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7189015/ https://www.ncbi.nlm.nih.gov/pubmed/32391021 http://dx.doi.org/10.3389/fimmu.2020.00741 |
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author | Junqueira-Kipnis, Ana Paula Trentini, Monalisa Martins Marques Neto, Lázaro Moreira Kipnis, André |
author_facet | Junqueira-Kipnis, Ana Paula Trentini, Monalisa Martins Marques Neto, Lázaro Moreira Kipnis, André |
author_sort | Junqueira-Kipnis, Ana Paula |
collection | PubMed |
description | It has been shown that neutrophils drive NK cells to activate DCs while NK cells regulate neutrophils survival. In response to mycobacteria, NK cells proliferate and produces IFN-γ, that appears to regulate the neutrophilic inflammatory responses to both M. tuberculosis infection and BCG vaccination. Although the role of neutrophils in the immune response to tuberculosis is a matter of debate, neutrophils were shown to be crucial to induce specific response against mc(2)-CMX vaccine. The objective of this study was to investigate the interplay between NK cells and neutrophils in regard to the development of a protective immune response against M. tuberculosis. Depletion of NK cells during vaccination did not alter the total number of neutrophils or DCs, but reduced the number of activated DCs, thus reducing the generation of Th1 specific immune responses and the protection conferred by mc(2)-CMX and BCG vaccines. However, only in mc(2)-CMX vaccination that neutrophil depletion interfered with the NK cell numbers and protection. In conclusion, it was shown that only when both NK and neutrophils were present, specific Th1 response and protection was achieved by mc(2)-CMX vaccine, while neutrophils although activated upon BCG vaccination were not necessary for the induced protection. |
format | Online Article Text |
id | pubmed-7189015 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71890152020-05-08 Live Vaccines Have Different NK Cells and Neutrophils Requirements for the Development of a Protective Immune Response Against Tuberculosis Junqueira-Kipnis, Ana Paula Trentini, Monalisa Martins Marques Neto, Lázaro Moreira Kipnis, André Front Immunol Immunology It has been shown that neutrophils drive NK cells to activate DCs while NK cells regulate neutrophils survival. In response to mycobacteria, NK cells proliferate and produces IFN-γ, that appears to regulate the neutrophilic inflammatory responses to both M. tuberculosis infection and BCG vaccination. Although the role of neutrophils in the immune response to tuberculosis is a matter of debate, neutrophils were shown to be crucial to induce specific response against mc(2)-CMX vaccine. The objective of this study was to investigate the interplay between NK cells and neutrophils in regard to the development of a protective immune response against M. tuberculosis. Depletion of NK cells during vaccination did not alter the total number of neutrophils or DCs, but reduced the number of activated DCs, thus reducing the generation of Th1 specific immune responses and the protection conferred by mc(2)-CMX and BCG vaccines. However, only in mc(2)-CMX vaccination that neutrophil depletion interfered with the NK cell numbers and protection. In conclusion, it was shown that only when both NK and neutrophils were present, specific Th1 response and protection was achieved by mc(2)-CMX vaccine, while neutrophils although activated upon BCG vaccination were not necessary for the induced protection. Frontiers Media S.A. 2020-04-22 /pmc/articles/PMC7189015/ /pubmed/32391021 http://dx.doi.org/10.3389/fimmu.2020.00741 Text en Copyright © 2020 Junqueira-Kipnis, Trentini, Marques Neto and Kipnis. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Junqueira-Kipnis, Ana Paula Trentini, Monalisa Martins Marques Neto, Lázaro Moreira Kipnis, André Live Vaccines Have Different NK Cells and Neutrophils Requirements for the Development of a Protective Immune Response Against Tuberculosis |
title | Live Vaccines Have Different NK Cells and Neutrophils Requirements for the Development of a Protective Immune Response Against Tuberculosis |
title_full | Live Vaccines Have Different NK Cells and Neutrophils Requirements for the Development of a Protective Immune Response Against Tuberculosis |
title_fullStr | Live Vaccines Have Different NK Cells and Neutrophils Requirements for the Development of a Protective Immune Response Against Tuberculosis |
title_full_unstemmed | Live Vaccines Have Different NK Cells and Neutrophils Requirements for the Development of a Protective Immune Response Against Tuberculosis |
title_short | Live Vaccines Have Different NK Cells and Neutrophils Requirements for the Development of a Protective Immune Response Against Tuberculosis |
title_sort | live vaccines have different nk cells and neutrophils requirements for the development of a protective immune response against tuberculosis |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7189015/ https://www.ncbi.nlm.nih.gov/pubmed/32391021 http://dx.doi.org/10.3389/fimmu.2020.00741 |
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