The renaissance of complement therapeutics

被引:301
作者
Ricklin, Daniel [1 ]
Mastellos, Dimitrios C. [2 ]
Reis, Edimara S. [3 ]
Lambris, John D. [3 ]
机构
[1] Univ Basel, Dept Pharmaceut Sci, Klingelbergstr 50, CH-4056 Basel, Switzerland
[2] Natl Ctr Sci Res Demokritos, Patr Gregoriou E & 27 Neapoleos Str, Athens 15341, Greece
[3] Univ Penn, Dept Pathol & Lab Med, 401 Stellar Chance,422 Curie Blvd, Philadelphia, PA 19104 USA
基金
美国国家科学基金会; 美国国家卫生研究院; 瑞士国家科学基金会;
关键词
PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA; HEMOLYTIC-UREMIC SYNDROME; ANTIBODY-MEDIATED REJECTION; ANTI-C5; MONOCLONAL-ANTIBODY; CORE CURRICULUM 2015; C3 INHIBITOR CP40; KIDNEY-TRANSPLANTATION; INNATE IMMUNITY; COMPONENT C3; IN-VITRO;
D O I
10.1038/nrneph.2017.156
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
The increasing number of clinical conditions that involve a pathological contribution from the complement system-many of which affect the kidneys-has spurred a regained interest in therapeutic options to modulate this host defence pathway. Molecular insight, technological advances, and the first decade of clinical experience with the complement-specific drug eculizumab, have contributed to a growing confidence in therapeutic complement inhibition. More than 20 candidate drugs that target various stages of the complement cascade are currently being evaluated in clinical trials, and additional agents are in preclinical development. Such diversity is clearly needed in view of the complex and distinct involvement of complement in a wide range of clinical conditions, including rare kidney disorders, transplant rejection and haemodialysis-induced inflammation. The existing drugs cannot be applied to all complement-driven diseases, and each indication has to be assessed individually. Alongside considerations concerning optimal points of intervention and economic factors, patient stratification will become essential to identify the best complement-specific therapy for each individual patient. This Review provides an overview of the therapeutic concepts, targets and candidate drugs, summarizes insights from clinical trials, and reflects on existing challenges for the development of complement therapeutics for kidney diseases and beyond.
引用
收藏
页码:26 / 47
页数:22
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