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Common Genetic Variants in the Complement System and their Potential Link with Disease Susceptibility and Outcome of Invasive Bacterial Infection
- Source :
- Journal of Innate Immunity, 12, 131-141, Journal of Innate Immunity, 12, 2, pp. 131-141
- Publication Year :
- 2020
-
Abstract
- Contains fulltext : 218852.pdf (Publisher’s version ) (Open Access) 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.
- Subjects :
- 0301 basic medicine
lnfectious Diseases and Global Health Radboud Institute for Molecular Life Sciences [Radboudumc 4]
Single-nucleotide polymorphism
Inflammation
Review Article
Neisseria meningitidis
medicine.disease_cause
Pneumococcal Infections
03 medical and health sciences
0302 clinical medicine
Streptococcus pneumoniae
medicine
Immunology and Allergy
Humans
Genetic Predisposition to Disease
biology
Genetic Variation
Complement System Proteins
Complement (complexity)
Complement system
Meningococcal Infections
030104 developmental biology
030228 respiratory system
Immunology
Humoral immunity
biology.protein
Antibody
medicine.symptom
Subjects
Details
- ISSN :
- 1662811X
- Database :
- OpenAIRE
- Journal :
- Journal of Innate Immunity, 12, 131-141, Journal of Innate Immunity, 12, 2, pp. 131-141
- Accession number :
- edsair.doi.dedup.....8260361ac7850347b8cfa032c50eb80a