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10.1051/medsci/2020168

http://scihub22266oqcxt.onion/10.1051/medsci/2020168
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32960167!ä!32960167

suck abstract from ncbi

pmid32960167      Med+Sci+(Paris) 2020 ; 36 (10): 908-913
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  • Immunite adaptative contre le virus SARS-CoV-2 #MMPMID32960167
  • Combadiere B
  • Med Sci (Paris) 2020[Oct]; 36 (10): 908-913 PMID32960167show ga
  • The impact of host adaptive immune response on COVID-19 has now become a critical issue in absence of specific therapy and immunotherapies. In SARS CoV-2 infection, the immune response is thought to contribute both to the pathogenesis of the disease and to protection during its resolution. While mild cases develop an immune response that contributes to host protection, immunity of severely infected patients is a balance between harmful and protective immune responses. The severity of the disease has raised many questions about the kinetic, amplitude and the quality of adaptive immunity to the virus and its generation during the early phases of infection in severe, mild and asymptomatic patients. The role of antibody and CD4(+) and CD8(+) T cell responses have been studied and the development of an adaptive immunity seems to correlate with convalescence. The bioinformatics study of the T and B epitopes of coronaviruses has raised the question of the existence of cross-immunity between SARS-CoV-2 and other coronaviruses such as MERS-CoV and SARS-CoV. In this review, we discuss the adaptive immune responses and their potential roles in protection during COVID-19.
  • |Adaptive Immunity/*physiology[MESH]
  • |Betacoronavirus/*immunology[MESH]
  • |COVID-19[MESH]
  • |COVID-19 Serotherapy[MESH]
  • |Coronavirus Infections/epidemiology/*immunology/therapy[MESH]
  • |Humans[MESH]
  • |Immunity, Cellular/physiology[MESH]
  • |Immunity, Humoral/physiology[MESH]
  • |Immunization, Passive[MESH]
  • |Pandemics[MESH]
  • |Pneumonia, Viral/epidemiology/*immunology/therapy[MESH]
  • |SARS-CoV-2[MESH]


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