Age-related macular degeneration: A disease of extracellular complement amplification

Age-related macular degeneration (AMD) is a major cause of vision impairment in the Western World, and with the aging world population, its incidence is increasing. As of today, for the majority of patients, no treatment exists. Multiple genetic and biochemical studies have shown a strong association with components in the complement system and AMD, and evidence suggests a major role of remodeling of the extracellular matrix underlying the outer blood/retinal barrier. As part of the innate immune system, the complement cascade acts as a first-line defense against pathogens, and upon activation, its amplification loop ensures a strong, rapid, and sustained response. Excessive activation, however, can lead to host tissue damage and cause complement-associated diseases like AMD. AMD patients present with aberrant activation of the alternative pathway, especially in ocular tissues but also on a systemic level. Here, we review the latest findings of complement activation in AMD, and we will discuss in vivo observations made in human tissue, cellular models, the potential synergy of different AMD-associated pathways, and conclude on current clinical trials and the future outlook.

Automated summary

Age-related macular degeneration (AMD) is a major cause of vision impairment, but currently there is no effective treatment for the majority of patients. Studies have shown that the complement system and remodeling of the extracellular matrix play a significant role in AMD. Excessive activation of the complement system can lead to tissue damage and complement-associated diseases like AMD. The latest findings suggest abnormal activation of the alternative pathway in AMD patients, which has important implications for future clinical trials and treatment prospects.