Properdin: New roles in pattern recognition and target clearance
Open accessAbstract
Properdin was first described over 50 years ago by Louis Pillemer and his collaborators as a vital component of an antibody-independent complement activation pathway. In the 1970s properdin was shown to be a stabilizing component of the alternative pathway convertases, the central enzymes of the complement cascade. Recently we have reported that properdin can also bind to target cells and microbes, provide a platform for convertase assembly and function, and promote target phagocytosis. Evidence is emerging that suggests that properdin interacts with a network of target ligands, phagocyte receptors, and serum regulators. Here we review the new findings and their possible implications.
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Neutrophils store properdin, a critical positive regulator of the alternative pathway.
“not only store properdin (60), a critical positive regulator of the alternative pathway (61)”
From Pre-existing humoral immunity and complement pathway contribute to immunogenicity of adeno-associated virus (AAV) vector in human blood (2022) · cites this paper as [61]
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- Authors
- Kemper, C., & Hourcade, D. E.
- Affiliations
- King's College London (GB)
- Washington University in St. Louis (US)
- Corresponding author
- Hourcade, Dennis E.
- Venue
- Molecular Immunology
- Publisher
- Elsevier BV
- Published
- 2008-10
- Volume
- 45
- Issue
- 16
- Pages
- 4048-4056
- ISSN
- 0161-5890 (ISSN-L)
- PMC
- PMC2628304
- OpenAlex
- W2067172213
- Cited by
- 95
- References
- 97
- Citations by year
- 2026: 3 · 2025: 1 · 2023: 2 · 2022: 4 · 2021: 4 · 2020: 2 · 2019: 4 · 2018: 8 · 2017: 7 · 2016: 6 · 2015: 5 · 2014: 6 · 2013: 5 · 2012: 7
- FWCI
- 0.76
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Molecular Immunology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Research Portal (King's College London) (submittedVersion)
- Funders
- National Institutes of Health
- National Institute of Allergy and Infectious Diseases (R01 AI05143, R01AI051436)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Complement system in diseases
- Life Sciences › Immunology and Microbiology › Immunology › Biomarkers in Disease Mechanisms
- Health Sciences › Medicine › Genetics › Coagulation, Bradykinin, Polyphosphates, and Angioedema
- Keywords
- properdin, alternative complement pathway, pattern recognition, phagocytosis, target cell binding, antibody-independent complement activation
- MeSH terms
- Animals, Complement System Proteins, Complement Pathway, Alternative, Humans, Properdin, Models, Immunological
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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