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Changes in T cell effector functions over an 8-year period with TNF antagonists in patients with chronic inflammatory rheumatic diseases

The aim of the study was to clarify the effect of long-term anti-TNF therapy on T cell function in patients with rheumatologic immune-mediated inflammatory diseases (IMID). The production of IFNγ by T cells was evaluated at baseline and after 1, 2, 4, and 8 years of anti-TNF agents by means of a Qua...

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Autores principales: Sauzullo, Ilaria, Scrivo, Rossana, Sessa, Paola, Mengoni, Fabio, Vullo, Vincenzo, Valesini, Guido, Mastroianni, Claudio Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5959893/
https://www.ncbi.nlm.nih.gov/pubmed/29777119
http://dx.doi.org/10.1038/s41598-018-26097-x
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author Sauzullo, Ilaria
Scrivo, Rossana
Sessa, Paola
Mengoni, Fabio
Vullo, Vincenzo
Valesini, Guido
Mastroianni, Claudio Maria
author_facet Sauzullo, Ilaria
Scrivo, Rossana
Sessa, Paola
Mengoni, Fabio
Vullo, Vincenzo
Valesini, Guido
Mastroianni, Claudio Maria
author_sort Sauzullo, Ilaria
collection PubMed
description The aim of the study was to clarify the effect of long-term anti-TNF therapy on T cell function in patients with rheumatologic immune-mediated inflammatory diseases (IMID). The production of IFNγ by T cells was evaluated at baseline and after 1, 2, 4, and 8 years of anti-TNF agents by means of a QuantiFERON-TB Gold In-Tube assay. The T cell proliferation and surface co-expression of CD25/CD134 in response to phytohaemagglutinin together with the in vitro impact of anti-TNF therapy on the functional capacity of T cells were evaluated after 8 years from the onset of the biological treatment. Age-matched healthy donors were enrolled as controls. The quantitative mitogen-induced IFNγ responses significantly increased with respect to baseline at each time point, apart from the determination after 4 years. We found an increased expression of CD25/CD134 in CD4(+) compared to CD8(+) T cells both in patients and controls. The in vitro addition of anti-TNF agents induced a significant decrease of both the IFNγ response and of CD25/CD134, whereas no effect on the intensity of the proliferative response was observed. Our data provide a biological basis for the reassuring issues on the safety of long-term anti-TNF treatment in patients with IMID.
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spelling pubmed-59598932018-05-24 Changes in T cell effector functions over an 8-year period with TNF antagonists in patients with chronic inflammatory rheumatic diseases Sauzullo, Ilaria Scrivo, Rossana Sessa, Paola Mengoni, Fabio Vullo, Vincenzo Valesini, Guido Mastroianni, Claudio Maria Sci Rep Article The aim of the study was to clarify the effect of long-term anti-TNF therapy on T cell function in patients with rheumatologic immune-mediated inflammatory diseases (IMID). The production of IFNγ by T cells was evaluated at baseline and after 1, 2, 4, and 8 years of anti-TNF agents by means of a QuantiFERON-TB Gold In-Tube assay. The T cell proliferation and surface co-expression of CD25/CD134 in response to phytohaemagglutinin together with the in vitro impact of anti-TNF therapy on the functional capacity of T cells were evaluated after 8 years from the onset of the biological treatment. Age-matched healthy donors were enrolled as controls. The quantitative mitogen-induced IFNγ responses significantly increased with respect to baseline at each time point, apart from the determination after 4 years. We found an increased expression of CD25/CD134 in CD4(+) compared to CD8(+) T cells both in patients and controls. The in vitro addition of anti-TNF agents induced a significant decrease of both the IFNγ response and of CD25/CD134, whereas no effect on the intensity of the proliferative response was observed. Our data provide a biological basis for the reassuring issues on the safety of long-term anti-TNF treatment in patients with IMID. Nature Publishing Group UK 2018-05-18 /pmc/articles/PMC5959893/ /pubmed/29777119 http://dx.doi.org/10.1038/s41598-018-26097-x Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Sauzullo, Ilaria
Scrivo, Rossana
Sessa, Paola
Mengoni, Fabio
Vullo, Vincenzo
Valesini, Guido
Mastroianni, Claudio Maria
Changes in T cell effector functions over an 8-year period with TNF antagonists in patients with chronic inflammatory rheumatic diseases
title Changes in T cell effector functions over an 8-year period with TNF antagonists in patients with chronic inflammatory rheumatic diseases
title_full Changes in T cell effector functions over an 8-year period with TNF antagonists in patients with chronic inflammatory rheumatic diseases
title_fullStr Changes in T cell effector functions over an 8-year period with TNF antagonists in patients with chronic inflammatory rheumatic diseases
title_full_unstemmed Changes in T cell effector functions over an 8-year period with TNF antagonists in patients with chronic inflammatory rheumatic diseases
title_short Changes in T cell effector functions over an 8-year period with TNF antagonists in patients with chronic inflammatory rheumatic diseases
title_sort changes in t cell effector functions over an 8-year period with tnf antagonists in patients with chronic inflammatory rheumatic diseases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5959893/
https://www.ncbi.nlm.nih.gov/pubmed/29777119
http://dx.doi.org/10.1038/s41598-018-26097-x
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