Complement Factor D as a Strategic Target for Regulating the Alternative Complement Pathway
Frontiers in Immunology, ISSN: 1664-3224, Vol: 12, Page: 712572
2021
- 66Citations
- 103Captures
- 1Mentions
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations66
- Citation Indexes66
- 66
- Captures103
- Readers103
- 103
- Mentions1
- News Mentions1
- News1
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1Department of Medicine, University of Alberta; Division of Hematology, University of Alberta Hospital, Edmonton, Alberta, Canada; 2Department of Medicine (Hematology), University of Toronto, Division of
Review Description
The complement system is central to first-line defense against invading pathogens. However, excessive complement activation and/or the loss of complement regulation contributes to the development of autoimmune diseases, systemic inflammation, and thrombosis. One of the three pathways of the complement system, the alternative complement pathway, plays a vital role in amplifying complement activation and pathway signaling. Complement factor D, a serine protease of this pathway that is required for the formation of C3 convertase, is the rate-limiting enzyme. In this review, we discuss the function of factor D within the alternative pathway and its implication in both healthy physiology and disease. Because the alternative pathway has a role in many diseases that are characterized by excessive or poorly mediated complement activation, this pathway is an enticing target for effective therapeutic intervention. Nonetheless, although the underlying disease mechanisms of many of these complement-driven diseases are quite well understood, some of the diseases have limited treatment options or no approved treatments at all. Therefore, in this review we explore factor D as a strategic target for advancing therapeutic control of pathological complement activation.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85115662235&origin=inward; http://dx.doi.org/10.3389/fimmu.2021.712572; http://www.ncbi.nlm.nih.gov/pubmed/34566967; https://www.frontiersin.org/articles/10.3389/fimmu.2021.712572/full; https://dx.doi.org/10.3389/fimmu.2021.712572; https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2021.712572/full
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