Complementopathies and precision medicine

被引:78
作者
Gavriilaki, Eleni [1 ]
Brodsky, Robert A. [2 ]
机构
[1] G Papanicolaou Hosp, Hematol Dept, Thessaloniki, Greece
[2] Johns Hopkins Univ, Sch Med, Dept Med, Div Hematol, Baltimore, MD 21205 USA
关键词
HEMOLYTIC-UREMIC SYNDROME; PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA; CATASTROPHIC ANTIPHOSPHOLIPID SYNDROME; AUTOIMMUNE MYASTHENIA-GRAVIS; STEM-CELL TRANSPLANTATION; DECAY-ACCELERATING FACTOR; MEMBRANE ATTACK COMPLEX; MANNOSE-BINDING LECTIN; THROMBOTIC MICROANGIOPATHY; TERMINAL COMPLEMENT;
D O I
10.1172/JCI136094
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The renaissance of complement diagnostics and therapeutics has introduced precision medicine into a widened field of complement-mediated diseases. In particular, complement-mediated diseases (or complementopathies) with ongoing or published clinical trials of complement inhibitors include paroxysmal nocturnal hemoglobinuria, cold agglutinin disease, hemolytic uremic syndrome, nephropathies, HELLP syndrome, transplant-associated thrombotic microangiopathy, antiphospholipid antibody syndrome, myasthenia gravis, and neuromyelitis optica. Recognizing that this field is rapidly expanding, we aim to provide a state-of-the-art review of (a) current understanding of complement biology for the clinician, (b) novel insights into complement with potential applicability to clinical practice, (c) complement in disease across various disciplines (hematology, nephrology, obstetrics, transplantation, rheumatology, and neurology), and (d) the potential future of precision medicine. Better understanding of complement diagnostics and therapeutics will not only facilitate physicians treating patients in clinical practice but also provide the basis for future research toward precision medicine in this field.
引用
收藏
页码:2152 / 2163
页数:12
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