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Hemofiltration induces generation of leukocyte-derived CD31+/CD41− microvesicles in sepsis

BACKGROUND: Microvesicles (MV) are extracellular vesicles known to be associated with cellular activation and inflammation. Hemofiltration is an effective blood purification technique for patients with renal failure and possibly also eliminates inflammatory mediators in the setting of sepsis. On the...

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Autores principales: Lehner, Georg Franz, Harler, Ulrich, Feistritzer, Clemens, Haller, Viktoria Maria, Hasslacher, Julia, Bellmann, Romuald, Joannidis, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5583134/
https://www.ncbi.nlm.nih.gov/pubmed/28871391
http://dx.doi.org/10.1186/s13613-017-0312-3
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author Lehner, Georg Franz
Harler, Ulrich
Feistritzer, Clemens
Haller, Viktoria Maria
Hasslacher, Julia
Bellmann, Romuald
Joannidis, Michael
author_facet Lehner, Georg Franz
Harler, Ulrich
Feistritzer, Clemens
Haller, Viktoria Maria
Hasslacher, Julia
Bellmann, Romuald
Joannidis, Michael
author_sort Lehner, Georg Franz
collection PubMed
description BACKGROUND: Microvesicles (MV) are extracellular vesicles known to be associated with cellular activation and inflammation. Hemofiltration is an effective blood purification technique for patients with renal failure and possibly also eliminates inflammatory mediators in the setting of sepsis. On the other hand, proinflammatory stimuli are induced by blood contacting the artificial membrane during extracorporeal blood purification. In chronic dialysis patients a systemic increase in MV has been described. The aim of the study was to investigate whether hemofilter passage of blood in continuous veno-venous hemofiltration (CVVH) alters MV composition and levels in critically ill patients with sepsis. METHODS: Pre- and postfilter bloods as well as ultrafiltrate samples from intensive care unit patients with severe sepsis were obtained during CVVH with regional citrate anticoagulation. MV subtypes in blood were analyzed by high-sensitivity flow cytometry. Additionally, tissue factor (TF) levels and MV-associated TF activities as well as MV activities were quantified. All parameters were corrected for hemoconcentration applied during CVVH. RESULTS: Twelve patients were analyzed. A significant increase in presumably mostly leukocyte-derived CD31+/CD41− MV (1.32 (1.09–1.93)-fold [median (25th–75th quartiles)], p = 0.021) was observed post- to prefilter, whereas platelet-derived MV as well as AnnexinV-binding MV were unaltered. Increments of AnnexinV+, CD42b+ and CD31+/CD41− MV post- to prefilter correlated with filtration fraction (FF) (all p < 0.05). Significant reductions in MV activity [0.72 (0.62–0.84)-fold, p = 0.002] and TF level [0.95 (0.87–0.99)-fold, p = 0.0093] were detected postfilter compared to prefilter. No MV activity was measurable in ultrafiltrate samples. CONCLUSIONS: Despite clearing a fraction of small PS-exposing MV CVVH does not eliminate larger MV. Concurrently, CVVH induces the release of CD31+/CD4− MV that indicate leukocyte activation during hemofilter passage in septic patients. Increments of several MV subtypes within the hemofilter correlate with FF, which supports common recommendations to keep FF low. A fraction of TF is being cleared by CVVH via ultrafiltration. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13613-017-0312-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-55831342017-09-22 Hemofiltration induces generation of leukocyte-derived CD31+/CD41− microvesicles in sepsis Lehner, Georg Franz Harler, Ulrich Feistritzer, Clemens Haller, Viktoria Maria Hasslacher, Julia Bellmann, Romuald Joannidis, Michael Ann Intensive Care Research BACKGROUND: Microvesicles (MV) are extracellular vesicles known to be associated with cellular activation and inflammation. Hemofiltration is an effective blood purification technique for patients with renal failure and possibly also eliminates inflammatory mediators in the setting of sepsis. On the other hand, proinflammatory stimuli are induced by blood contacting the artificial membrane during extracorporeal blood purification. In chronic dialysis patients a systemic increase in MV has been described. The aim of the study was to investigate whether hemofilter passage of blood in continuous veno-venous hemofiltration (CVVH) alters MV composition and levels in critically ill patients with sepsis. METHODS: Pre- and postfilter bloods as well as ultrafiltrate samples from intensive care unit patients with severe sepsis were obtained during CVVH with regional citrate anticoagulation. MV subtypes in blood were analyzed by high-sensitivity flow cytometry. Additionally, tissue factor (TF) levels and MV-associated TF activities as well as MV activities were quantified. All parameters were corrected for hemoconcentration applied during CVVH. RESULTS: Twelve patients were analyzed. A significant increase in presumably mostly leukocyte-derived CD31+/CD41− MV (1.32 (1.09–1.93)-fold [median (25th–75th quartiles)], p = 0.021) was observed post- to prefilter, whereas platelet-derived MV as well as AnnexinV-binding MV were unaltered. Increments of AnnexinV+, CD42b+ and CD31+/CD41− MV post- to prefilter correlated with filtration fraction (FF) (all p < 0.05). Significant reductions in MV activity [0.72 (0.62–0.84)-fold, p = 0.002] and TF level [0.95 (0.87–0.99)-fold, p = 0.0093] were detected postfilter compared to prefilter. No MV activity was measurable in ultrafiltrate samples. CONCLUSIONS: Despite clearing a fraction of small PS-exposing MV CVVH does not eliminate larger MV. Concurrently, CVVH induces the release of CD31+/CD4− MV that indicate leukocyte activation during hemofilter passage in septic patients. Increments of several MV subtypes within the hemofilter correlate with FF, which supports common recommendations to keep FF low. A fraction of TF is being cleared by CVVH via ultrafiltration. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13613-017-0312-3) contains supplementary material, which is available to authorized users. Springer International Publishing 2017-09-04 /pmc/articles/PMC5583134/ /pubmed/28871391 http://dx.doi.org/10.1186/s13613-017-0312-3 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.
spellingShingle Research
Lehner, Georg Franz
Harler, Ulrich
Feistritzer, Clemens
Haller, Viktoria Maria
Hasslacher, Julia
Bellmann, Romuald
Joannidis, Michael
Hemofiltration induces generation of leukocyte-derived CD31+/CD41− microvesicles in sepsis
title Hemofiltration induces generation of leukocyte-derived CD31+/CD41− microvesicles in sepsis
title_full Hemofiltration induces generation of leukocyte-derived CD31+/CD41− microvesicles in sepsis
title_fullStr Hemofiltration induces generation of leukocyte-derived CD31+/CD41− microvesicles in sepsis
title_full_unstemmed Hemofiltration induces generation of leukocyte-derived CD31+/CD41− microvesicles in sepsis
title_short Hemofiltration induces generation of leukocyte-derived CD31+/CD41− microvesicles in sepsis
title_sort hemofiltration induces generation of leukocyte-derived cd31+/cd41− microvesicles in sepsis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5583134/
https://www.ncbi.nlm.nih.gov/pubmed/28871391
http://dx.doi.org/10.1186/s13613-017-0312-3
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