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Differential effects of Th17 cytokines during the response of neutrophils to Burkholderia cenocepacia outer membrane protein A

T helper 17 cells are involved in the immunopathology of cystic fibrosis. They play a key role in recruitment of neutrophils, which is the first line of defence against bacteria. Additionally, Burkholderia cenocepacia outer membrane protein A (OmpA) BCAL2958 is considered a potential protective epit...

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Autores principales: NADY, SOAD, ABDEL-RAHMAN, MONA, SOUSA, SILVIA A., LEITãO, JORGE H., MORAD, MOSTAFA, EL-HENNAMY, REHAB E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7050059/
https://www.ncbi.nlm.nih.gov/pubmed/32140053
http://dx.doi.org/10.5114/ceji.2019.92800
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author NADY, SOAD
ABDEL-RAHMAN, MONA
SOUSA, SILVIA A.
LEITãO, JORGE H.
MORAD, MOSTAFA
EL-HENNAMY, REHAB E.
author_facet NADY, SOAD
ABDEL-RAHMAN, MONA
SOUSA, SILVIA A.
LEITãO, JORGE H.
MORAD, MOSTAFA
EL-HENNAMY, REHAB E.
author_sort NADY, SOAD
collection PubMed
description T helper 17 cells are involved in the immunopathology of cystic fibrosis. They play a key role in recruitment of neutrophils, which is the first line of defence against bacteria. Additionally, Burkholderia cenocepacia outer membrane protein A (OmpA) BCAL2958 is considered a potential protective epitope for vaccine development. The present study aimed to investigate the neutrophil response to OmpA in the presence of Th17 cytokines, IL-17 and IL-22 at different times of activation. Neutrophils were isolated from whole blood of healthy volunteers and activated with OmpA in the presence of IL-17, IL-22 or both cytokines together. Supernatant was collected after 1 h, 2 h, 4 h, 8 h, and 12 h. Neutrophil activation was assessed by measuring MPO, TNF-α, elastase, hydrogen peroxide, catalase and NO. The results revealed that the combination of IL-17 and IL-22 cytokines induced the release of NE, catalase, H(2)O(2) and TNF-α from neutrophils activated with Burkholderia OmpA at late stages of activation. However, IL-22 alone or IL-17 alone decreased the myeloperoxidase (MPO), catalase and NE levels at early stages of neutrophil activation. The presence of IL-17 alone led to a significant increase in TNF-α level after 1 h and 12 h. However, the presence of IL-22 alone led to a significant increase in TNF-α level after only 1 h but a significant decrease after 8 h of activation was observed as compared to OmpA stimulated neutrophils. In conclusion, Th17 cytokines IL-17 and IL-22, have differential effects during the neutrophil response to Burkholderia OmpA.
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spelling pubmed-70500592020-03-05 Differential effects of Th17 cytokines during the response of neutrophils to Burkholderia cenocepacia outer membrane protein A NADY, SOAD ABDEL-RAHMAN, MONA SOUSA, SILVIA A. LEITãO, JORGE H. MORAD, MOSTAFA EL-HENNAMY, REHAB E. Cent Eur J Immunol Clinical Immunology T helper 17 cells are involved in the immunopathology of cystic fibrosis. They play a key role in recruitment of neutrophils, which is the first line of defence against bacteria. Additionally, Burkholderia cenocepacia outer membrane protein A (OmpA) BCAL2958 is considered a potential protective epitope for vaccine development. The present study aimed to investigate the neutrophil response to OmpA in the presence of Th17 cytokines, IL-17 and IL-22 at different times of activation. Neutrophils were isolated from whole blood of healthy volunteers and activated with OmpA in the presence of IL-17, IL-22 or both cytokines together. Supernatant was collected after 1 h, 2 h, 4 h, 8 h, and 12 h. Neutrophil activation was assessed by measuring MPO, TNF-α, elastase, hydrogen peroxide, catalase and NO. The results revealed that the combination of IL-17 and IL-22 cytokines induced the release of NE, catalase, H(2)O(2) and TNF-α from neutrophils activated with Burkholderia OmpA at late stages of activation. However, IL-22 alone or IL-17 alone decreased the myeloperoxidase (MPO), catalase and NE levels at early stages of neutrophil activation. The presence of IL-17 alone led to a significant increase in TNF-α level after 1 h and 12 h. However, the presence of IL-22 alone led to a significant increase in TNF-α level after only 1 h but a significant decrease after 8 h of activation was observed as compared to OmpA stimulated neutrophils. In conclusion, Th17 cytokines IL-17 and IL-22, have differential effects during the neutrophil response to Burkholderia OmpA. Termedia Publishing House 2020-01-20 2019 /pmc/articles/PMC7050059/ /pubmed/32140053 http://dx.doi.org/10.5114/ceji.2019.92800 Text en Copyright © 2019 Termedia http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0). License (http://creativecommons.org/licenses/by-nc-sa/4.0/)
spellingShingle Clinical Immunology
NADY, SOAD
ABDEL-RAHMAN, MONA
SOUSA, SILVIA A.
LEITãO, JORGE H.
MORAD, MOSTAFA
EL-HENNAMY, REHAB E.
Differential effects of Th17 cytokines during the response of neutrophils to Burkholderia cenocepacia outer membrane protein A
title Differential effects of Th17 cytokines during the response of neutrophils to Burkholderia cenocepacia outer membrane protein A
title_full Differential effects of Th17 cytokines during the response of neutrophils to Burkholderia cenocepacia outer membrane protein A
title_fullStr Differential effects of Th17 cytokines during the response of neutrophils to Burkholderia cenocepacia outer membrane protein A
title_full_unstemmed Differential effects of Th17 cytokines during the response of neutrophils to Burkholderia cenocepacia outer membrane protein A
title_short Differential effects of Th17 cytokines during the response of neutrophils to Burkholderia cenocepacia outer membrane protein A
title_sort differential effects of th17 cytokines during the response of neutrophils to burkholderia cenocepacia outer membrane protein a
topic Clinical Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7050059/
https://www.ncbi.nlm.nih.gov/pubmed/32140053
http://dx.doi.org/10.5114/ceji.2019.92800
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