Back to Search
Start Over
New Insights into the Role of the Complement System in Human Viral Diseases.
- Source :
-
Biomolecules [Biomolecules] 2022 Jan 28; Vol. 12 (2). Date of Electronic Publication: 2022 Jan 28. - Publication Year :
- 2022
-
Abstract
- The complement system (CS) is part of the human immune system, consisting of more than 30 proteins that play a vital role in the protection against various pathogens and diseases, including viral diseases. Activated via three pathways, the classical pathway (CP), the lectin pathway (LP), and the alternative pathway (AP), the complement system leads to the formation of a membrane attack complex (MAC) that disrupts the membrane of target cells, leading to cell lysis and death. Due to the increasing number of reports on its role in viral diseases, which may have implications for research on severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), this review aims to highlight significant progress in understanding and defining the role of the complement system in four groups of diseases of viral etiology: (1) respiratory diseases; (2) acute liver failure (ALF); (3) disseminated intravascular coagulation (DIC); and (4) vector-borne diseases (VBDs). Some of these diseases already present a serious global health problem, while others are a matter of concern and require the collaboration of relevant national services and scientists with the World Health Organization (WHO) to avoid their spread.
- Subjects :
- Animals
Disseminated Intravascular Coagulation immunology
Disseminated Intravascular Coagulation virology
Humans
Liver Failure, Acute immunology
Liver Failure, Acute virology
Respiratory Tract Diseases immunology
Respiratory Tract Diseases virology
Vector Borne Diseases immunology
Vector Borne Diseases virology
Complement System Proteins
Virus Diseases etiology
Subjects
Details
- Language :
- English
- ISSN :
- 2218-273X
- Volume :
- 12
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Biomolecules
- Publication Type :
- Academic Journal
- Accession number :
- 35204727
- Full Text :
- https://doi.org/10.3390/biom12020226