Involvement of Complement in Alzheimer's Disease: From Genetics Through Pathology to Therapeutic Strategies
- PMID: 39455500
- DOI: 10.1007/7854_2024_524
Involvement of Complement in Alzheimer's Disease: From Genetics Through Pathology to Therapeutic Strategies
Erratum in
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Correction to: Involvement of Complement in Alzheimer's Disease: From Genetics Through Pathology to Therapeutic Strategies.Curr Top Behav Neurosci. 2025;69:C1. doi: 10.1007/7854_2024_576. Curr Top Behav Neurosci. 2025. PMID: 39849280 No abstract available.
Abstract
Complement is a critical component of innate immunity, evolved to defend against pathogens and clear toxic debris ranging from dead and dying cells to immune complexes. These roles make complement a key player in homeostasis; however, complement has a dark side. When the rigid control mechanisms fail, complement becomes dysregulated, acting as a driver of inflammation and resultant pathology in numerous diseases. Roles of complement in Alzheimer's disease (AD) and other dementias have emerged in recent years, supported by genetic, biomarker and pathological evidence and animal model studies. Numerous questions remain regarding the precise roles of complement in the brain in health and disease, including where and when complement is expressed, how it contributes to immune defence and garbage disposal in the healthy brain, and exactly how complement contributes to pathology in dementias. In this brief review, we will summarise current knowledge on complement roles in brain, present the evidence implicating complement in AD and explore whether complement represents an attractive therapeutic target for AD.
Keywords: Biomarkers; Brain; Complement; Dementia; Genetics; Synapse; Therapeutics.
© 2024. The Author(s), under exclusive license to Springer Nature Switzerland AG.
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References
-
- ANX005 | ALZFORUM [Internet]. [cited 2024 Jun 17]. Available from: https://www.alzforum.org/therapeutics/anx005
-
- Apellis Pharmaceuticals, Inc. A phase 2, randomized, double-blind, placebo-controlled, multicenter study to evaluate the efficacy and safety of pegcetacoplan in subjects with amyotrophic lateral sclerosis (ALS) [Internet]. clinicaltrials.gov ; 2024 Feb [cited 2024 Jan 1]. Report No.: NCT04579666. Available from: https://clinicaltrials.gov/study/NCT04579666
-
- Bilkei-Gorzo A (2014) Genetic mouse models of brain ageing and Alzheimer’s disease. Pharmacol Ther 142(2):244–257 - PubMed
-
- Bohlson SS, Tenner AJ (2023) Complement in the brain: contributions to neuroprotection, neuronal plasticity, and neuroinflammation. Annu Rev Immunol 41:431–452 - PubMed
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