Cargando…
γδ T lymphocytes from cystic fibrosis patients and healthy donors are high TNF-α and IFN-γ-producers in response to Pseudomonas aeruginosa
BACKGROUND: γδ T cells have an important immunoregulatory and effector function through cytokine release. They are involved in the responses to Gram-negative bacterium and in protection of lung epithelium integrity. On the other hand, they have been implicated in airway inflammation. METHODS: The ai...
Autores principales: | , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2003
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC203157/ https://www.ncbi.nlm.nih.gov/pubmed/14525626 http://dx.doi.org/10.1186/1465-9921-4-9 |
_version_ | 1782120952287461376 |
---|---|
author | Raga, Salvador Julià, M Rosa Crespí, Catalina Figuerola, Joan Martínez, Natalia Milà, Joan Matamoros, Núria |
author_facet | Raga, Salvador Julià, M Rosa Crespí, Catalina Figuerola, Joan Martínez, Natalia Milà, Joan Matamoros, Núria |
author_sort | Raga, Salvador |
collection | PubMed |
description | BACKGROUND: γδ T cells have an important immunoregulatory and effector function through cytokine release. They are involved in the responses to Gram-negative bacterium and in protection of lung epithelium integrity. On the other hand, they have been implicated in airway inflammation. METHODS: The aim of the present work was to study intracytoplasmic IL-2, IL-4, IFN-γ and TNF-α production by γδ and αβ T lymphocytes from cystic fibrosis patients and healthy donors in response to Pseudomonas aeruginosa (PA). Flow cytometric detection was performed after peripheral blood mononuclear cells (PBMC) culture with a cytosolic extract from PA and restimulation with phorbol ester plus ionomycine. Proliferative responses, activation markers and receptor usage of γδ T cells were also evaluated. RESULTS: The highest production of cytokine was of TNF-α and IFN-γ, γδ being better producers than αβ. No differences were found between patients and controls. The Vγ9δ2 subset of γδ T cells was preferentially expanded. CD25 and CD45RO expression by the αβ T subset and PBMC proliferative response to PA were defective in cystic fibrosis lymphocytes. CONCLUSION: Our results support the hypothesis that γδ T lymphocytes play an important role in the immune response to PA and in the chronic inflammatory lung reaction in cystic fibrosis patients. They do not confirm the involvement of a supressed Th1 cytokine response in the pathogenesis of this disease. |
format | Text |
id | pubmed-203157 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-2031572003-10-02 γδ T lymphocytes from cystic fibrosis patients and healthy donors are high TNF-α and IFN-γ-producers in response to Pseudomonas aeruginosa Raga, Salvador Julià, M Rosa Crespí, Catalina Figuerola, Joan Martínez, Natalia Milà, Joan Matamoros, Núria Respir Res Research BACKGROUND: γδ T cells have an important immunoregulatory and effector function through cytokine release. They are involved in the responses to Gram-negative bacterium and in protection of lung epithelium integrity. On the other hand, they have been implicated in airway inflammation. METHODS: The aim of the present work was to study intracytoplasmic IL-2, IL-4, IFN-γ and TNF-α production by γδ and αβ T lymphocytes from cystic fibrosis patients and healthy donors in response to Pseudomonas aeruginosa (PA). Flow cytometric detection was performed after peripheral blood mononuclear cells (PBMC) culture with a cytosolic extract from PA and restimulation with phorbol ester plus ionomycine. Proliferative responses, activation markers and receptor usage of γδ T cells were also evaluated. RESULTS: The highest production of cytokine was of TNF-α and IFN-γ, γδ being better producers than αβ. No differences were found between patients and controls. The Vγ9δ2 subset of γδ T cells was preferentially expanded. CD25 and CD45RO expression by the αβ T subset and PBMC proliferative response to PA were defective in cystic fibrosis lymphocytes. CONCLUSION: Our results support the hypothesis that γδ T lymphocytes play an important role in the immune response to PA and in the chronic inflammatory lung reaction in cystic fibrosis patients. They do not confirm the involvement of a supressed Th1 cytokine response in the pathogenesis of this disease. BioMed Central 2003 2003-09-08 /pmc/articles/PMC203157/ /pubmed/14525626 http://dx.doi.org/10.1186/1465-9921-4-9 Text en Copyright © 2003 Raga et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL. |
spellingShingle | Research Raga, Salvador Julià, M Rosa Crespí, Catalina Figuerola, Joan Martínez, Natalia Milà, Joan Matamoros, Núria γδ T lymphocytes from cystic fibrosis patients and healthy donors are high TNF-α and IFN-γ-producers in response to Pseudomonas aeruginosa |
title | γδ T lymphocytes from cystic fibrosis patients and healthy donors are high TNF-α and IFN-γ-producers in response to Pseudomonas aeruginosa |
title_full | γδ T lymphocytes from cystic fibrosis patients and healthy donors are high TNF-α and IFN-γ-producers in response to Pseudomonas aeruginosa |
title_fullStr | γδ T lymphocytes from cystic fibrosis patients and healthy donors are high TNF-α and IFN-γ-producers in response to Pseudomonas aeruginosa |
title_full_unstemmed | γδ T lymphocytes from cystic fibrosis patients and healthy donors are high TNF-α and IFN-γ-producers in response to Pseudomonas aeruginosa |
title_short | γδ T lymphocytes from cystic fibrosis patients and healthy donors are high TNF-α and IFN-γ-producers in response to Pseudomonas aeruginosa |
title_sort | γδ t lymphocytes from cystic fibrosis patients and healthy donors are high tnf-α and ifn-γ-producers in response to pseudomonas aeruginosa |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC203157/ https://www.ncbi.nlm.nih.gov/pubmed/14525626 http://dx.doi.org/10.1186/1465-9921-4-9 |
work_keys_str_mv | AT ragasalvador gdtlymphocytesfromcysticfibrosispatientsandhealthydonorsarehightnfaandifngproducersinresponsetopseudomonasaeruginosa AT juliamrosa gdtlymphocytesfromcysticfibrosispatientsandhealthydonorsarehightnfaandifngproducersinresponsetopseudomonasaeruginosa AT crespicatalina gdtlymphocytesfromcysticfibrosispatientsandhealthydonorsarehightnfaandifngproducersinresponsetopseudomonasaeruginosa AT figuerolajoan gdtlymphocytesfromcysticfibrosispatientsandhealthydonorsarehightnfaandifngproducersinresponsetopseudomonasaeruginosa AT martineznatalia gdtlymphocytesfromcysticfibrosispatientsandhealthydonorsarehightnfaandifngproducersinresponsetopseudomonasaeruginosa AT milajoan gdtlymphocytesfromcysticfibrosispatientsandhealthydonorsarehightnfaandifngproducersinresponsetopseudomonasaeruginosa AT matamorosnuria gdtlymphocytesfromcysticfibrosispatientsandhealthydonorsarehightnfaandifngproducersinresponsetopseudomonasaeruginosa |