Pregnancy is associated with a simultaneous but independent increase in circulating CD177pos and immature low-density granulocytes.

IF 3.6 3区 医学 Q3 CELL BIOLOGY
Agnes Dahlstrand Rudin, Agnes Torell, Jordan Popovic, Marit Stockfelt, Bo Jacobsson, Anna Rudin, Karin Christenson, Anna-Carin Lundell, Johan Bylund
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引用次数: 0

Abstract

The neutrophil marker CD177 (NB1, HNA-2a) is expressed by 0-100% of circulating neutrophils in any given donor, dividing neutrophils into two distinct subpopulations (CD177pos and CD177neg). High proportions of CD177pos blood neutrophils have been linked to both systemic infections and a range of inflammatory pathologies, but whether this is a cause or a consequence of disease is not known. Many conditions displaying elevated CD177pos neutrophil proportions are also accompanied by the presence of circulating low-density granulocytes (LDGs). Accordingly, it is tempting to speculate that these two events are connected, i.e., that proportions of CD177pos neutrophils increase as a result of an enlarged pool of circulating LDGs. A temporary increase in CD177pos neutrophils, in combination with the presence of LDGs has been reported during pregnancy. The present study aimed to investigate whether elevated proportions of CD177pos neutrophils in peripheral blood from pregnant women can be attributed to the presence of LDGs. We found that LDGs were indeed present in pregnancy and included both immature, and activated mature neutrophils. The proportion of CD177pos LDGs increased over time during pregnancy and correlated with a simultaneous increase in immature cells. However, a majority of immature neutrophils were CD177neg, meaning that increased release of immature cells cannot explain the increased proportions of the CD177pos subtype. Therefore, although LDGs and CD177pos neutrophils are expanded simultaneously during pregnancy these events occur independent from each other.

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来源期刊
Journal of Leukocyte Biology
Journal of Leukocyte Biology 医学-免疫学
CiteScore
11.50
自引率
0.00%
发文量
358
审稿时长
2 months
期刊介绍: JLB is a peer-reviewed, academic journal published by the Society for Leukocyte Biology for its members and the community of immunobiologists. The journal publishes papers devoted to the exploration of the cellular and molecular biology of granulocytes, mononuclear phagocytes, lymphocytes, NK cells, and other cells involved in host physiology and defense/resistance against disease. Since all cells in the body can directly or indirectly contribute to the maintenance of the integrity of the organism and restoration of homeostasis through repair, JLB also considers articles involving epithelial, endothelial, fibroblastic, neural, and other somatic cell types participating in host defense. Studies covering pathophysiology, cell development, differentiation and trafficking; fundamental, translational and clinical immunology, inflammation, extracellular mediators and effector molecules; receptors, signal transduction and genes are considered relevant. Research articles and reviews that provide a novel understanding in any of these fields are given priority as well as technical advances related to leukocyte research methods.
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