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Neutrophil phenotypes implicated in the pathophysiology of post-traumatic sepsis
BACKGROUND: The disruption of immune homeostasis after trauma is a major cause of post-traumatic organ dysfunction and/or sepsis. Recently, a variety of neutrophil phenotypes with distinct functions have been identified and suggested as involved in various clinical conditions. The association betwee...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9757139/ https://www.ncbi.nlm.nih.gov/pubmed/36530874 http://dx.doi.org/10.3389/fmed.2022.982399 |
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author | Mizugaki, Asumi Wada, Takeshi Tsuchida, Takumi Oda, Yoshitaka Kayano, Katsuhide Yamakawa, Kazuma Tanaka, Shinya |
author_facet | Mizugaki, Asumi Wada, Takeshi Tsuchida, Takumi Oda, Yoshitaka Kayano, Katsuhide Yamakawa, Kazuma Tanaka, Shinya |
author_sort | Mizugaki, Asumi |
collection | PubMed |
description | BACKGROUND: The disruption of immune homeostasis after trauma is a major cause of post-traumatic organ dysfunction and/or sepsis. Recently, a variety of neutrophil phenotypes with distinct functions have been identified and suggested as involved in various clinical conditions. The association between neutrophil phenotypes and post-traumatic immunodeficiency has also been reported, yet the specific neutrophil phenotypes and their functional significance in post-traumatic sepsis have not been fully clarified. Therefore, we sought to investigate neutrophil phenotypic changes in a murine model, as these may hold prognostic value in post-traumatic sepsis. MATERIALS AND METHODS: Third-degree burns affecting 25% of the body surface area were used to establish trauma model, and sepsis was induced 24 h later through cecal ligation and puncture (CLP). The Burn/CLP post-traumatic sepsis model and the Sham/CLP control model were established to assess the immunological status after trauma. Histopathological evaluation was performed on the spleen, liver, kidneys, and lung tissues. Immunological evaluation included the assessment of neutrophil markers using mass cytometry as well as cytokine measurements in serum and ascitic fluid through multiplex analysis using LUMINEX(®). RESULTS: The Burn/CLP group had a lower survival rate than the Sham/CLP group. Histopathological examination revealed an impaired immune response and more advanced organ damage in the Burn/CLP group. Furthermore, the Burn/CLP group exhibited higher levels of transforming growth factor-beta 1 in the blood and generally lower levels of cytokines than the Sham/CLP group. CD11b, which is involved in neutrophil adhesion and migration, was highly expressed on neutrophils in the Burn/CLP group. The expression of CD172a, which is related to the inhibition of phagocytosis, was also upregulated on neutrophils in the Burn/CLP group. The expression of sialic acid-binding lg-like lectin F and CD68 also differed between the two groups. CONCLUSION: Different neutrophil phenotypes were observed between Burn/CLP and Sham/CLP groups, suggesting that neutrophils are implicated in the immune imbalance following trauma. However, further studies are needed to prove the causal relationships between neutrophil phenotypes and outcomes, including survival rate and organ dysfunction. |
format | Online Article Text |
id | pubmed-9757139 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97571392022-12-17 Neutrophil phenotypes implicated in the pathophysiology of post-traumatic sepsis Mizugaki, Asumi Wada, Takeshi Tsuchida, Takumi Oda, Yoshitaka Kayano, Katsuhide Yamakawa, Kazuma Tanaka, Shinya Front Med (Lausanne) Medicine BACKGROUND: The disruption of immune homeostasis after trauma is a major cause of post-traumatic organ dysfunction and/or sepsis. Recently, a variety of neutrophil phenotypes with distinct functions have been identified and suggested as involved in various clinical conditions. The association between neutrophil phenotypes and post-traumatic immunodeficiency has also been reported, yet the specific neutrophil phenotypes and their functional significance in post-traumatic sepsis have not been fully clarified. Therefore, we sought to investigate neutrophil phenotypic changes in a murine model, as these may hold prognostic value in post-traumatic sepsis. MATERIALS AND METHODS: Third-degree burns affecting 25% of the body surface area were used to establish trauma model, and sepsis was induced 24 h later through cecal ligation and puncture (CLP). The Burn/CLP post-traumatic sepsis model and the Sham/CLP control model were established to assess the immunological status after trauma. Histopathological evaluation was performed on the spleen, liver, kidneys, and lung tissues. Immunological evaluation included the assessment of neutrophil markers using mass cytometry as well as cytokine measurements in serum and ascitic fluid through multiplex analysis using LUMINEX(®). RESULTS: The Burn/CLP group had a lower survival rate than the Sham/CLP group. Histopathological examination revealed an impaired immune response and more advanced organ damage in the Burn/CLP group. Furthermore, the Burn/CLP group exhibited higher levels of transforming growth factor-beta 1 in the blood and generally lower levels of cytokines than the Sham/CLP group. CD11b, which is involved in neutrophil adhesion and migration, was highly expressed on neutrophils in the Burn/CLP group. The expression of CD172a, which is related to the inhibition of phagocytosis, was also upregulated on neutrophils in the Burn/CLP group. The expression of sialic acid-binding lg-like lectin F and CD68 also differed between the two groups. CONCLUSION: Different neutrophil phenotypes were observed between Burn/CLP and Sham/CLP groups, suggesting that neutrophils are implicated in the immune imbalance following trauma. However, further studies are needed to prove the causal relationships between neutrophil phenotypes and outcomes, including survival rate and organ dysfunction. Frontiers Media S.A. 2022-12-02 /pmc/articles/PMC9757139/ /pubmed/36530874 http://dx.doi.org/10.3389/fmed.2022.982399 Text en Copyright © 2022 Mizugaki, Wada, Tsuchida, Oda, Kayano, Yamakawa and Tanaka. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Medicine Mizugaki, Asumi Wada, Takeshi Tsuchida, Takumi Oda, Yoshitaka Kayano, Katsuhide Yamakawa, Kazuma Tanaka, Shinya Neutrophil phenotypes implicated in the pathophysiology of post-traumatic sepsis |
title | Neutrophil phenotypes implicated in the pathophysiology of post-traumatic sepsis |
title_full | Neutrophil phenotypes implicated in the pathophysiology of post-traumatic sepsis |
title_fullStr | Neutrophil phenotypes implicated in the pathophysiology of post-traumatic sepsis |
title_full_unstemmed | Neutrophil phenotypes implicated in the pathophysiology of post-traumatic sepsis |
title_short | Neutrophil phenotypes implicated in the pathophysiology of post-traumatic sepsis |
title_sort | neutrophil phenotypes implicated in the pathophysiology of post-traumatic sepsis |
topic | Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9757139/ https://www.ncbi.nlm.nih.gov/pubmed/36530874 http://dx.doi.org/10.3389/fmed.2022.982399 |
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