Common Genetic Variants in the Complement System and their Potential Link with Disease Susceptibility and Outcome of Invasive Bacterial Infection.
Publication year
2020Source
Journal of Innate Immunity, 12, 2, (2020), pp. 131-141ISSN
Publication type
Article / Letter to editor
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Organization
Paediatrics
Laboratory Medicine
Journal title
Journal of Innate Immunity
Volume
vol. 12
Issue
iss. 2
Page start
p. 131
Page end
p. 141
Subject
Radboudumc 4: lnfectious Diseases and Global Health RIMLS: Radboud Institute for Molecular Life Sciences; Laboratory Medicine - Radboud University Medical Center; Paediatrics - Radboud University Medical CenterAbstract
Streptococcus pneumoniae and Neisseria meningitidis are pathogens that frequently colonize the nasopharynx in an asymptomatic manner but are also a cause of invasive bacterial infections mainly in young children. The complement system plays a crucial role in humoral immunity, complementing the ability of antibodies to clear microbes, thereby protecting the host against bacterial infections, including S. pneumoniae and N. meningitidis. While it is widely accepted that complement deficiencies due to rare genetic variants increase the risk for invasive bacterial infection, not much is known about the common genetic variants in the complement system in relation to disease susceptibility. In this review, we provide an overview of the effects of common genetic variants on complement activation and on complement-mediated inflammation.
This item appears in the following Collection(s)
- Academic publications [243984]
- Electronic publications [130873]
- Faculty of Medical Sciences [92811]
- Open Access publications [105044]
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