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10.1016/j.virusres.2021.198347

http://scihub22266oqcxt.onion/10.1016/j.virusres.2021.198347
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suck abstract from ncbi


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pmid33631219      Virus+Res 2021 ; 299 (ä): 198347
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  • Protection against COVID-19 in African population: Immunology, genetics, and malaria clues for therapeutic targets #MMPMID33631219
  • Altable M; de la Serna JM
  • Virus Res 2021[Jul]; 299 (ä): 198347 PMID33631219show ga
  • BACKGROUND: There is a marked discrepancy between SARS-CoV-2 seroprevalence and COVID-19 cases and deaths in Africa. MAIN: SARS-CoV-2 stimulates humoral and cellular immunity systems, as well as mitogen-activated protein kinase (MAPK) and nuclear NF-kB signalling pathways, which regulate inflammatory gene expression and immune cell differentiation. The result is pro-inflammatory cytokines release, hyperinflammatory condition, and cytokine storm, which provoke severe lung alterations that can lead to multi-organ failure in COVID-19. Multiple genetic and immunologic factors may contribute to the severity of COVID-19 in African individuals when compared to the rest of the global population. In this article, the role of malaria, NF-kB and MAPK pathways, caspase-12 expression, high level of LAIR-1-containing antibodies, and differential glycophorins (GYPA/B) expression in COVID-19 are discussed. CONCLUSION: Understanding pathophysiological mechanisms can help identify target points for drugs and vaccines development against COVID-19. To our knowledge, this is the first study that explores this link and proposes a biological and molecular answer to the epidemiologic discrepancy in COVID-19 in Africa.
  • |Africa/epidemiology[MESH]
  • |COVID-19/epidemiology/ethnology/*genetics/*immunology[MESH]
  • |Caspase 12/genetics/immunology[MESH]
  • |Glycophorins/genetics/immunology[MESH]
  • |Humans[MESH]
  • |Malaria/epidemiology/ethnology/*genetics/*immunology[MESH]
  • |NF-kappa B/immunology[MESH]
  • |Receptors, Immunologic/genetics/immunology[MESH]
  • |SARS-CoV-2/immunology[MESH]


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