Increased phagocytosis capacity of circulating neutrophils in patients on continuous flow ventricular assist device support.
Increased phagocytosis capacity of circulating neutrophils in patients on continuous flow ventricular assist device support.
复制标题
在连续流心室辅助装置支持下患者循环中性粒细胞的吞噬能力增加。
DOI:
10.1111/aor.14693
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发表时间:
2023
影响因子:
2.4
通讯作者:
Wu,ZhongjunJ
中科院分区:
文献类型:
--
作者:
Awad,MorcosA;Sun,Wenji;Han,Dong;Griffith,BartleyP;Wu,ZhongjunJ
BackgroundNeutrophils take part in the innate immune response, phagocytosis, and pro‐inflammatory cytokine release. The phagocytic capacity of circulating neutrophils in patients on continuous flow (CF) ventricular assist device (VAD) has not been well studied.MethodsBlood samples from 14 patients undergoing CF‐VAD implantation were collected and analyzed preoperatively (at baseline) and on postoperative days (POD) 3, 7, 14, and 28. Flow cytometry was used to assess the surface expression levels of CD62L, CD162, and macrophage antigen‐1 (MAC‐1) and neutrophil phagocytic capacity. Interleukin 1 (IL1), IL6, IL8, TNF‐α, neutrophil elastase, and myeloperoxidase in plasma were measured using enzyme‐linked immunosorbent assays.ResultsAmong the 14 patients, seven patients had preoperative bridge device support. Relative to baseline, patients with no bridge device had elevated leukocyte count and neutrophil elastase by POD3 which normalized by POD7. Neutrophil activation level, IL6, IL8, and TNF‐α increased by POD3 and sustained elevated levels for 7–14 days postoperatively. Elevated neutrophil phagocytic capacity persisted even until POD28. Similar patterns were observed in patients on a preoperative bridge device.ConclusionsNeutrophil activation and phagocytic capacity increased in response to VAD support, while inflammatory cytokines remain elevated for up to 2 weeks postoperatively. These findings may indicate that VAD implantation elicits circulating neutrophils to an abnormal preemptive phagocytotic phenotype.
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DOI:
--
发表时间:
2001
期刊:
ASAIO journal (1992)
影响因子:
--
作者:
M. Loebe;A. Koster;S. Sänger;E. Potapov;H. Kuppe;G. Noon;R. Hetzer
通讯作者:
R. Hetzer
影响因子:
6
作者:
Gemma Radley;I. L. Pieper;C. R. Robinson;Sabrina Alì;Mostafa Beshr;O. Bodger;C. Thornton
通讯作者:
C. Thornton
影响因子:
2.4
作者:
Woolley,JoshuaR;Teuteberg,JeffreyJ;Bermudez,ChristianA;Bhama,JayK;Lockard,KathleenL;Kormos,RobertL;Wagner,WilliamR
通讯作者:
Wagner,WilliamR
DOI:
10.1177/0391398818784276
发表时间:
2018
期刊:
The International Journal of Artificial Organs
影响因子:
--
作者:
G. Bhat;G. Yost;Kamel Ibrahim;P. Pappas;A. Tatooles
通讯作者:
A. Tatooles
DOI:
10.1073/pnas.110463197
发表时间:
2000
影响因子:
11.1
作者:
Shive,MS;Salloum,ML;Anderson,JM
通讯作者:
Anderson,JM