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About:
Leukocyte function assessed via serial microlitre sampling of peripheral blood from sepsis patients correlates with disease severity
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research paper
schema:ScholarlyArticle
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Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Leukocyte function assessed via serial microlitre sampling of peripheral blood from sepsis patients correlates with disease severity
Creator
Higuera, Angelica
Pinilla-Vera, Mayra
Baron, Rebecca
Krishnamoorthy, Nandini
Abdulnour, Raja-Elie
Benson, Maura
Duvall, Melody
Engstrom, Braden
Han, Jongyoon
Jundi, Bakr
Lee, Do-Hyun
Lee, Jaemyon
Levy, Bruce
Ryu, Hyunryul
Voldman, Joel
Source
PMC
abstract
Dysregulated leukocyte responses underlie the pathobiology of sepsis, which is a leading cause of death. However, measures of leukocyte function are not routinely available in clinical care. Here we report the development and testing of an inertial microfluidic system for the label-free isolation and downstream functional assessment of leukocytes from 50 μl of peripheral blood. We used the system to assess leukocyte phenotype and function in serial samples from 18 hospitalized patients with sepsis and 10 healthy subjects. The sepsis samples had significantly higher levels of CD16(dim) and CD16(−) neutrophils and CD16(+) ‘intermediate’ monocytes, as well as significantly lower levels of neutrophil-elastase release, O(2)(−) production and phagolysosome formation. Repeated sampling of sepsis patients over 7 days showed that leukocyte activation (measured by isodielectric separation) and leukocyte phenotype and function were significantly more predictive of the clinical course than complete-blood-count parameters. We conclude that the serial assessment of leukocyte function in microlitre blood volumes is feasible and that it provides significantly more prognostic information than leukocyte counting.
has issue date
2019-11-11
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)
bibo:doi
10.1038/s41551-019-0473-5
bibo:pmid
31712645
has license
no-cc
sha1sum (hex)
c836e422a09d3e536679f468bc0dc6186e58335b
schema:url
https://doi.org/10.1038/s41551-019-0473-5
resource representing a document's title
Leukocyte function assessed via serial microlitre sampling of peripheral blood from sepsis patients correlates with disease severity
has PubMed Central identifier
PMC6899180
has PubMed identifier
31712645
schema:publication
Nat Biomed Eng
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covid:c836e422a09d3e536679f468bc0dc6186e58335b#body_text
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schema:about
of
named entity 'intermediate'
named entity 'function'
named entity 'sampling'
named entity 'samples'
named entity 'monocytes'
named entity 'separation'
named entity 'microlitre'
named entity 'responses'
named entity 'function'
named entity 'patients'
named entity 'sepsis'
named entity 'phenotype'
named entity 'samples'
named entity 'predictive'
named entity 'leukocytes'
named entity 'CD16'
named entity 'sepsis'
named entity 'phenotype'
named entity 'leukocyte'
named entity 'microlitre'
named entity 'leukocyte'
named entity 'leukocyte'
named entity 'neutrophil'
named entity 'sepsis'
named entity 'peripheral blood'
named entity 'leukocytes'
named entity 'ANOVA'
named entity 'sepsis'
named entity 'CD16'
named entity 'peripheral blood'
named entity 'pathobiology'
named entity 'PMNs'
named entity 'pathobiology'
named entity 'CD14'
named entity 'PMNs'
named entity 'flow cytometry'
named entity 'IDP'
named entity 'microfluidics'
named entity 'microfluidics'
named entity 'elastase'
named entity 'leukocyte activation'
named entity 'ice water'
named entity 'operation time'
named entity 'syringe pumps'
named entity 'flow resistance'
named entity 'clinical outcomes'
named entity 'biomarkers'
named entity 'leukocyte activation'
named entity 'cell adhesion molecules'
named entity 'CBC'
named entity 'sepsis'
named entity 'leukocyte'
named entity 'intensive care unit'
named entity '7.5'
named entity 'superoxide anion'
named entity 'sepsis'
named entity 'PMNs'
named entity 'CD42b'
named entity 'CBC'
named entity 'Physiology'
named entity 'sepsis'
named entity 'supernatant'
named entity 'plasma'
named entity 'PMNs'
named entity 'sepsis'
named entity 'mesenchymal stem cells'
named entity 'Chronic Health'
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