Intracellular expression of granzymes A, B, K and M in blood lymphocyte subsets of critically ill patients with or without sepsis
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2021-08
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Abstract
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.
Keywords
granzymes, infection, inflammation, sepsis, Sepsis/metabolism, CD8-Positive T-Lymphocytes/metabolism, Humans, Middle Aged, Critical Illness, Granzymes/metabolism, Male, Killer Cells, Natural/metabolism, Female, Lymphocyte Subsets/metabolism, Lymphocyte Count/methods, Immunology and Allergy, Immunology, Journal Article, Clinical Trial, Research Support, Non-U.S. Gov't
Citation
García-Laorden, M I, Hoogendijk, A J, Wiewel, M A, van Vught, L A, Schultz, M J, Bovenschen, N, de Vos, A F & van der Poll, T 2021, 'Intracellular expression of granzymes A, B, K and M in blood lymphocyte subsets of critically ill patients with or without sepsis', Clinical and Experimental Immunology, vol. 205, no. 2, pp. 222-231. https://doi.org/10.1111/cei.13601