| Literature DB >> 33063546 |
Roberta Romano1, Giuliana Giardino1, Emilia Cirillo1, Rosaria Prencipe1, Claudio Pignata1.
Abstract
The complement system is a multi-functional system representing the first line host defense against pathogens in innate immune response, through three different pathways. Impairment of its function, consisting in deficiency or excessive deregulated activation, may lead to severe systemic infections or autoimmune disorders. These diseases may be inherited or acquired. Despite many diagnostic tools are currently available, ranging from traditional, such as hemolytic or ELISA based assays, to innovative ones, like next generation sequencing techniques, these diseases are often not recognized. As for therapeutic aspects, strategies based on the use of targeted drugs are now widespread. The aim of this review is to present an updated overview of complement system pathophysiology, clinical implications of its dysfunction and to summarize diagnostic and therapeutic approaches.Entities:
Keywords: Neisseria meningitidis; Angioedema; complement system; complement system deficiencies; paroxysmal nocturnal hemoglobinuria
Year: 2020 PMID: 33063546 DOI: 10.1080/08830185.2020.1833877
Source DB: PubMed Journal: Int Rev Immunol ISSN: 0883-0185 Impact factor: 5.311