Nature Immunology, Journal Year: 2022, Volume and Issue: 23(2), P. 275 - 286
Published: Jan. 31, 2022
Language: Английский
Nature Immunology, Journal Year: 2022, Volume and Issue: 23(2), P. 275 - 286
Published: Jan. 31, 2022
Language: Английский
Nature Immunology, Journal Year: 2021, Volume and Issue: 23(1), P. 62 - 74
Published: Nov. 11, 2021
Language: Английский
Citations
159Journal of Autoimmunity, Journal Year: 2020, Volume and Issue: 116, P. 102560 - 102560
Published: Oct. 30, 2020
Language: Английский
Citations
152Critical Care Medicine, Journal Year: 2021, Volume and Issue: 49(12), P. 2042 - 2057
Published: July 13, 2021
Coronavirus disease 2019 is a heterogeneous most frequently causing respiratory tract infection, which can induce failure and multiple organ dysfunction syndrome in its severe forms. The prevalence of coronavirus 2019-related sepsis still unclear; we aimed to describe this systematic review.
Language: Английский
Citations
146Pharmacological Reviews, Journal Year: 2021, Volume and Issue: 73(2), P. 792 - 827
Published: March 9, 2021
The complement system was discovered at the end of 19th century as a heat-labile plasma component that "complemented" antibodies in killing microbes, hence name "complement." Complement is also part innate immune system, protecting host by recognition pathogen-associated molecular patterns. However, multifunctional far beyond infectious defense. It contributes to organ development, such sculpting neuron synapses, promoting tissue regeneration and repair, rapidly engaging synergizing with number processes, including hemostasis leading thromboinflammation. double-edged sword. Although it usually protects host, may cause damage when dysregulated or overactivated, systemic inflammatory reaction seen trauma sepsis severe coronavirus disease 2019 (COVID-19). Damage-associated patterns generated during ischemia-reperfusion injuries (myocardial infarction, stroke, transplant dysfunction) chronic neurologic rheumatic activate complement, thereby increasing damaging inflammation. Despite long list diseases potential for ameliorating modulation, only few rare are approved clinical treatment targeting complement. Those currently being efficiently treated include paroxysmal nocturnal hemoglobinuria, atypical hemolytic-uremic syndrome, myasthenia gravis, neuromyelitis optica spectrum disorders. Rare diseases, unfortunately, preclude robust trials. evidence pathogenetic driver many more common suggests an opportunity future therapy, which, however, requires trials; one ongoing example COVID-19 disease. current review aims discuss pathogenesis pharmacological strategies treat these complement-targeted therapies.
Language: Английский
Citations
137Nature Immunology, Journal Year: 2022, Volume and Issue: 23(2), P. 275 - 286
Published: Jan. 31, 2022
Language: Английский
Citations
137