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10.1016/j.humimm.2021.01.007

http://scihub22266oqcxt.onion/10.1016/j.humimm.2021.01.007
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suck abstract from ncbi


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pmid33632561      Hum+Immunol 2021 ; 82 (4): 264-269
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  • Pharmacological approach for the reduction of inflammatory and prothrombotic hyperactive state in COVID-19 positive patients by acting on complement cascade #MMPMID33632561
  • Vitiello A; La Porta R; D'Aiuto V; Ferrara F
  • Hum Immunol 2021[Apr]; 82 (4): 264-269 PMID33632561show ga
  • The novel Coronavirus SARS-CoV-2 is the viral pathogen responsible for the ongoing global pandemic, COVID-19 (Coronavirus disease 2019). To date, the data recorded indicate 1.62 Mln deaths and 72.8 Mln people infected (WHO situation report Dec 2020). On December 27, the first anti-COVID-19 vaccinations started in Europe. There are no direct antivirals against SARS-CoV-2. Understanding the pathophysiological and inflammatory/immunological processes of SARS-CoV-2 infection is essential to identify new drug therapies. In the most severe COVID-19 cases, an unregulated immunological/inflammatory system results in organ injury that can be fatal to the host in some cases. Pharmacologic approaches to normalize the unregulated inflammatory/immunologic response is an important therapeutic solution. Evidence associates a non-regulation of the "complement system" as one of the causes of generalized inflammation causing multi-organ dysfunction. Serum levels of a complement cascade mediator, factor "C5a", have been found in high concentrations in the blood of COVID-19 patients with severe disease. In this article we discuss the correlation between complement system and COVID-19 infection and pharmacological solutions directed to regulate.
  • |*COVID-19 Drug Treatment[MESH]
  • |Antibodies, Monoclonal, Humanized/therapeutic use[MESH]
  • |COVID-19/pathology/physiopathology[MESH]
  • |Complement Activation/*drug effects/immunology[MESH]
  • |Complement C3a/*antagonists & inhibitors/immunology[MESH]
  • |Complement C5a/*antagonists & inhibitors/immunology[MESH]
  • |Complement Inactivating Agents/*therapeutic use[MESH]
  • |Humans[MESH]


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