血小板
抗磷脂综合征
中性粒细胞胞外陷阱
医学
免疫学
抗体
内科学
炎症
作者
Somanathapura K. NaveenKumar,Ajay Tambralli,Bruna de Moraes Mazetto,Srilakshmi Yalavarthi,Wenying Liang,Claire K. Hoy,Cyrus Sarosh,Christine E. Rysenga,Caroline H. Ranger,Caroline E. Vance,Jacqueline A. Madison,Fernanda Andrade Orsi,Suman L. Sood,Jordan K. Schaefer,Yu Zuo,Jason S. Knight
出处
期刊:Blood
[Elsevier BV]
日期:2024-01-18
卷期号:143 (12): 1193-1197
被引量:7
标识
DOI:10.1182/blood.2023022097
摘要
Many patients with antiphospholipid syndrome had decreased ectonucleotidase activity on neutrophils and platelets, which enabled extracellular nucleotides to trigger neutrophil-platelet aggregates. This phenotype was replicated by treating healthy neutrophils and platelets with patient-derived antiphospholipid antibodies or ectonucleotidase inhibitors.
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