The case for complement component 5 as a target in neurodegenerative disease

被引:9
作者
Stennett, Amelia [1 ]
Friston, Kallie [1 ]
Harris, Claire L. [2 ]
Wollman, Adam J. M. [2 ]
Bronowska, Agnieszka K. [1 ]
Madden, Katrina S. [1 ,2 ]
机构
[1] Newcastle Univ, Sch Nat & Environm Sci, Newcastle Upon Tyne NE1 7RU, England
[2] Newcastle Univ, Fac Med Sci, Newcastle Upon Tyne NE2 4HH, England
基金
英国工程与自然科学研究理事会;
关键词
Complement pathway; complement component 5; drug discovery; neurodegenerative disease; neuroinflammation; MEMBRANE ATTACK COMPLEX; MOUSE MODEL; MENINGOCOCCAL DISEASE; INHIBITOR ECULIZUMAB; PARKINSONS-DISEASE; SMALL MOLECULES; MURINE MODELS; DOUBLE-BLIND; SPINAL-CORD; FACTOR C5A;
D O I
10.1080/14728222.2023.2177532
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
IntroductionComplement-based drug discovery is undergoing a renaissance, empowered by new advances in structural biology, complement biology and drug development. Certain components of the complement pathway, particularly C1q and C3, have been extensively studied in the context of neurodegenerative disease, and established as key therapeutic targets. C5 also has huge therapeutic potential in this arena, with its druggability clearly demonstrated by the success of C5-inhibitor eculizumab.Areas coveredWe will discuss the evidence supporting C5 as a target in neurodegenerative disease, along with the current progress in developing different classes of C5 inhibitors and the gaps in knowledge that will help progress in the field.Expert opinionValidation of C5 as a therapeutic target for neurodegenerative disease would represent a major step forward for complement therapeutics research and has the potential to furnish disease-modifying drugs for millions of patients suffering worldwide. Key hurdles that need to be overcome for this to be achieved are understanding how C5a and C5b should be targeted to bring therapeutic benefit and demonstrating the ability to target C5 without creating vulnerability to infection in patients. This requires greater biological elucidation of its precise role in disease pathogenesis, supported by better chemical/biological tools.
引用
收藏
页码:97 / 109
页数:13
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