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Intracellular expression of granzymes A, B, K and M in blood lymphocyte subsets of critically ill patients with or without sepsis
Sepsis is a complex syndrome related to an infection‐induced exaggerated inflammatory response, which is associated with a high mortality. Granzymes (Gzm) are proteases mainly found in cytotoxic lymphocytes that not only have a role in target cell death, but also as mediators of infection and inflam...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8274148/ https://www.ncbi.nlm.nih.gov/pubmed/33866542 http://dx.doi.org/10.1111/cei.13601 |
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author | García‐Laorden, M. Isabel Hoogendijk, Arie J. Wiewel, Maryse A. van Vught, Lonneke A. Schultz, Marcus J. Bovenschen, Niels de Vos, Alex F. van der Poll, Tom |
author_facet | García‐Laorden, M. Isabel Hoogendijk, Arie J. Wiewel, Maryse A. van Vught, Lonneke A. Schultz, Marcus J. Bovenschen, Niels de Vos, Alex F. van der Poll, Tom |
author_sort | García‐Laorden, M. Isabel |
collection | PubMed |
description | Sepsis is a complex syndrome related to an infection‐induced exaggerated inflammatory response, which is associated with a high mortality. Granzymes (Gzm) are proteases mainly found in cytotoxic lymphocytes that not only have a role in target cell death, but also as mediators of infection and inflammation. In this study we sought to analyse the intracellular expression of GzmA, B, M and K by flow cytometry in diverse blood lymphocyte populations from 22 sepsis patients, 12 non‐infected intensive care unit (ICU) patients and 32 healthy controls. Additionally, we measured GzmA and B plasma levels. Both groups of patients presented decreased percentage of natural killer (NK) cells expressing GzmA, B and M relative to healthy controls, while sepsis patients showed an increased proportion of CD8(+) T cells expressing GzmB compared to controls. Expression of GzmK remained relatively unaltered between groups. Extracellular levels of GzmB were increased in non‐infected ICU patients relative to sepsis patients and healthy controls. Our results show differential alterations in intracellular expression of Gzm in sepsis patients and non‐infected critically ill patients compared to healthy individuals depending on the lymphocyte population and on the Gzm. |
format | Online Article Text |
id | pubmed-8274148 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82741482021-07-14 Intracellular expression of granzymes A, B, K and M in blood lymphocyte subsets of critically ill patients with or without sepsis García‐Laorden, M. Isabel Hoogendijk, Arie J. Wiewel, Maryse A. van Vught, Lonneke A. Schultz, Marcus J. Bovenschen, Niels de Vos, Alex F. van der Poll, Tom Clin Exp Immunol ORIGINAL ARTICLES Sepsis is a complex syndrome related to an infection‐induced exaggerated inflammatory response, which is associated with a high mortality. Granzymes (Gzm) are proteases mainly found in cytotoxic lymphocytes that not only have a role in target cell death, but also as mediators of infection and inflammation. In this study we sought to analyse the intracellular expression of GzmA, B, M and K by flow cytometry in diverse blood lymphocyte populations from 22 sepsis patients, 12 non‐infected intensive care unit (ICU) patients and 32 healthy controls. Additionally, we measured GzmA and B plasma levels. Both groups of patients presented decreased percentage of natural killer (NK) cells expressing GzmA, B and M relative to healthy controls, while sepsis patients showed an increased proportion of CD8(+) T cells expressing GzmB compared to controls. Expression of GzmK remained relatively unaltered between groups. Extracellular levels of GzmB were increased in non‐infected ICU patients relative to sepsis patients and healthy controls. Our results show differential alterations in intracellular expression of Gzm in sepsis patients and non‐infected critically ill patients compared to healthy individuals depending on the lymphocyte population and on the Gzm. John Wiley and Sons Inc. 2021-05-27 2021-08 /pmc/articles/PMC8274148/ /pubmed/33866542 http://dx.doi.org/10.1111/cei.13601 Text en © 2021 The Authors. Clinical & Experimental Immunology published by John Wiley & Sons Ltd on behalf of British Society for Immunology https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | ORIGINAL ARTICLES García‐Laorden, M. Isabel Hoogendijk, Arie J. Wiewel, Maryse A. van Vught, Lonneke A. Schultz, Marcus J. Bovenschen, Niels de Vos, Alex F. van der Poll, Tom Intracellular expression of granzymes A, B, K and M in blood lymphocyte subsets of critically ill patients with or without sepsis |
title | Intracellular expression of granzymes A, B, K and M in blood lymphocyte subsets of critically ill patients with or without sepsis |
title_full | Intracellular expression of granzymes A, B, K and M in blood lymphocyte subsets of critically ill patients with or without sepsis |
title_fullStr | Intracellular expression of granzymes A, B, K and M in blood lymphocyte subsets of critically ill patients with or without sepsis |
title_full_unstemmed | Intracellular expression of granzymes A, B, K and M in blood lymphocyte subsets of critically ill patients with or without sepsis |
title_short | Intracellular expression of granzymes A, B, K and M in blood lymphocyte subsets of critically ill patients with or without sepsis |
title_sort | intracellular expression of granzymes a, b, k and m in blood lymphocyte subsets of critically ill patients with or without sepsis |
topic | ORIGINAL ARTICLES |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8274148/ https://www.ncbi.nlm.nih.gov/pubmed/33866542 http://dx.doi.org/10.1111/cei.13601 |
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