Neutrophils as drivers of vascular injury in sickle cell disease

被引:5
|
作者
Torres, Lidiane S. [1 ,2 ]
Hidalgo, Andres [3 ,4 ,5 ]
机构
[1] Albert Einstein Coll Med, Ruth L & David S Gottesman Inst Stem Cell & Regen, Bronx, NY 10467 USA
[2] Albert Einstein Coll Med, Dept Cell Biol, Bronx, NY 10467 USA
[3] Ctr Nacl Invest Cardiovasc Carlos III, Area Cell & Dev Biol, Madrid, Spain
[4] Yale Univ, Sch Med, Vasc Biol & Therapeut Program, New Haven, CT USA
[5] Yale Univ, Sch Med, Dept Immunobiol, New Haven, CT USA
基金
美国国家卫生研究院;
关键词
cell adhesion; endothelium; hemolysis; inflammation; vaso-occlusion; COLONY-STIMULATING FACTOR; GLYCOPROTEIN IB-ALPHA; EXTRACELLULAR TRAPS; PULMONARY-HYPERTENSION; ADHESION MOLECULES; ENDOTHELIAL-CELLS; FETAL-HEMOGLOBIN; INTEGRIN MAC-1; BONE-MARROW; GRANULOCYTE;
D O I
10.1111/imr.13146
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
While neutrophils are the main effectors of protective innate immune responses, they are also key players in inflammatory pathologies. Sickle cell disease (SCD) is a genetic blood disorder in which red blood cells (RBCs) are constantly destroyed in the circulation which generates a highly inflammatory environment that culminates in vascular occlusions. Vaso-occlusion is the hallmark of SCD and a predictor of disease severity. Neutrophils initiate and propagate SCD-related vaso-occlusion through adhesive interactions with the activated and dysfunctional endothelium, sickle RBCs, and platelets, leading to acute and chronic complications that progress to irreversible organ damage and ultimately death. The use of SCD humanized mouse models, in combination with in vivo imaging techniques, has emerged as a fundamental tool to understand the dynamics of neutrophils under complex inflammatory contexts and their contribution to vascular injury in SCD. In this review, we discuss the various mechanisms by which circulating neutrophils sense and respond to the wide range of stimuli present in the blood of SCD patients and mice. We argue that the central role of neutrophils in SCD can be rationalized to develop targets for the management of clinical complications in SCD patients.
引用
收藏
页码:302 / 312
页数:11
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