TY - JOUR
T1 - Analyzing Neutrophil Morphology, Mechanics, and Motility in Sepsis
T2 - Options and Challenges for Novel Bedside Technologies
AU - Zonneveld, Rens
AU - Molema, Grietje
AU - Plötz, Frans B
PY - 2016/1
Y1 - 2016/1
N2 - Objective: Alterations in neutrophil morphology (size, shape, and composition), mechanics (deformability), and motility (chemotaxis and migration) have been observed during sepsis. We combine summarizing features of neutrophil morphology, mechanics, and motility that change during sepsis with an investigation into their clinical utility as markers for sepsis through measurement with novel technologies.Data Sources: We performed an initial literature search in MEDLINE using search terms neutrophil, morphology, mechanics, dynamics, motility, mobility, spreading, polarization, migration, and chemotaxis. We then combined the results with sepsis and septic shock. We scanned bibliographies of included articles to identify additional articles.Study Selection and Data Extraction: Final selection was done after the authors reviewed recovered articles. We included articles based on their relevance for our review topic.Data Synthesis: When compared with resting conditions, sepsis causes an increase in circulating numbers of larger, more rigid neutrophils that show diminished granularity, migration, and chemotaxis. Combined measurement of these variables could provide a more complete view on neutrophil phenotype manifestation. For that purpose, sophisticated automated hematology analyzers, microscopy, and bedside microfluidic devices provide clinically feasible, high-throughput, and cost-limiting means.Conclusions: We propose that integration of features of neutrophil morphology, mechanics, and motility with these new analytical methods can be useful as markers for diagnosis, prognosis, and monitoring of sepsis and may even contribute to basic understanding of its pathophysiology.
AB - Objective: Alterations in neutrophil morphology (size, shape, and composition), mechanics (deformability), and motility (chemotaxis and migration) have been observed during sepsis. We combine summarizing features of neutrophil morphology, mechanics, and motility that change during sepsis with an investigation into their clinical utility as markers for sepsis through measurement with novel technologies.Data Sources: We performed an initial literature search in MEDLINE using search terms neutrophil, morphology, mechanics, dynamics, motility, mobility, spreading, polarization, migration, and chemotaxis. We then combined the results with sepsis and septic shock. We scanned bibliographies of included articles to identify additional articles.Study Selection and Data Extraction: Final selection was done after the authors reviewed recovered articles. We included articles based on their relevance for our review topic.Data Synthesis: When compared with resting conditions, sepsis causes an increase in circulating numbers of larger, more rigid neutrophils that show diminished granularity, migration, and chemotaxis. Combined measurement of these variables could provide a more complete view on neutrophil phenotype manifestation. For that purpose, sophisticated automated hematology analyzers, microscopy, and bedside microfluidic devices provide clinically feasible, high-throughput, and cost-limiting means.Conclusions: We propose that integration of features of neutrophil morphology, mechanics, and motility with these new analytical methods can be useful as markers for diagnosis, prognosis, and monitoring of sepsis and may even contribute to basic understanding of its pathophysiology.
KW - automated hematology analyzers
KW - microfluidic devices
KW - migration
KW - morphology
KW - neutrophils
KW - sepsis
KW - RESPIRATORY-DISTRESS-SYNDROME
KW - C-REACTIVE PROTEIN
KW - FLOW-CYTOMETRY
KW - NEONATAL SEPSIS
KW - TRANSLATIONAL APPLICATIONS
KW - CHEMOTACTIC FUNCTION
KW - EXTRACELLULAR TRAPS
KW - CLINICAL-PRACTICE
KW - DISEASE SEVERITY
KW - SEPTIC PATIENTS
U2 - 10.1097/CCM.0000000000001266
DO - 10.1097/CCM.0000000000001266
M3 - Article
C2 - 26296143
SN - 0090-3493
VL - 44
SP - 218
EP - 228
JO - Critical Care Medicine
JF - Critical Care Medicine
IS - 1
ER -