Detailed Information on Publication Record
2021
Polymorphonuclear Cells Show Features of Dysfunctional Activation During Fatal Sepsis
HORTOVÁ KOHOUTKOVÁ, Marcela, Marco ZUANI DE, Petra LÁZNIČKOVÁ, Kamila BENDICKOVA, Ondřej MRKVA et. al.Basic information
Original name
Polymorphonuclear Cells Show Features of Dysfunctional Activation During Fatal Sepsis
Authors
HORTOVÁ KOHOUTKOVÁ, Marcela (203 Czech Republic), Marco ZUANI DE, Petra LÁZNIČKOVÁ (203 Czech Republic, belonging to the institution), Kamila BENDICKOVA (203 Czech Republic), Ondřej MRKVA (203 Czech Republic), Ivana ANDREJČINOVÁ (703 Slovakia, belonging to the institution), Alexandra MÝTNIKOVÁ (703 Slovakia), Ondrej POLANSKY (203 Czech Republic), Kamila KOCI (203 Czech Republic), Veronika TOMÁŠKOVÁ (203 Czech Republic, belonging to the institution), Vladimír ŠRÁMEK (203 Czech Republic, belonging to the institution), Martin HELÁN (203 Czech Republic, belonging to the institution) and Jan FRIČ (203 Czech Republic, guarantor)
Edition
Frontiers in Immunology, LAUSANNE, FRONTIERS MEDIA SA, 2021, 1664-3224
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30102 Immunology
Country of publisher
Switzerland
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 8.786
RIV identification code
RIV/00216224:14110/21:00120224
Organization unit
Faculty of Medicine
UT WoS
000735284800001
Keywords in English
sepsis; polymorphonuclears; septic shock; transcriptomics; proteomics; dysfunctionality
Tags
International impact, Reviewed
Změněno: 12/1/2023 09:36, Mgr. Tereza Miškechová
Abstract
V originále
Sepsis and septic shock remain leading causes of morbidity and mortality for patients in the intensive care unit. During the early phase, immune cells produce various cytokines leading to prompt activation of the immune system. Polymorphonuclear leukocytes (PMNs) respond to different signals producing inflammatory factors and executing their antimicrobial mechanisms, resulting in the engulfment and elimination of invading pathogens. However, excessive activation caused by various inflammatory signals produced during sepsis progression can lead to the alteration of PMN signaling and subsequent defects in their functionality. Here, we analyzed samples from 34 patients in septic shock, focusing on PMNs gene expression and proteome changes associated with septic shock. We revealed that, compared to those patients who survived longer than five days, PMNs from patients who had fulminant sepsis were characterized by a dysfunctional hyper-activation, show altered metabolism, and recent exit from the cell cycle and signs of cellular lifespan. We believe that this multi-omics approach, although limited, pinpoints the alterations in PMNs' functionality, which may be rescued by targeted treatments.
Links
LM2018132, research and development project |
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NU21-06-00408, research and development project |
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