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10.1038/s41598-021-03273-0

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suck abstract from ncbi


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pmid34887501      Sci+Rep 2021 ; 11 (1): 23713
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  • The potential of COVID-19 patients sera to cause antibody-dependent enhancement of infection and IL-6 production #MMPMID34887501
  • Shimizu J; Sasaki T; Yamanaka A; Ichihara Y; Koketsu R; Samune Y; Cruz P; Sato K; Tanga N; Yoshimura Y; Murakami A; Yamada M; Itoi K; Nakayama EE; Miyazaki K; Shioda T
  • Sci Rep 2021[Dec]; 11 (1): 23713 PMID34887501show ga
  • Since the emergence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), many vaccine trials have been initiated. An important goal of vaccination is the development of neutralizing antibody (Ab) against SARS-CoV-2. However, the possible induction of antibody-dependent enhancement (ADE) of infection, which is known for other coronaviruses and dengue virus infections, is a particular concern in vaccine development. Here, we demonstrated that human iPS cell-derived, immortalized, and ACE2- and TMPRSS2-expressing myeloid cell lines are useful as host cells for SARS-CoV-2 infection. The established cell lines were cloned and screened based on their function in terms of susceptibility to SARS-CoV-2-infection or IL-6 productivity. Using the resulting K-ML2 (AT) clone 35 for SARS-CoV-2-infection or its subclone 35-40 for IL-6 productivity, it was possible to evaluate the potential of sera from severe COVID-19 patients to cause ADE and to stimulate IL-6 production upon infection with SARS-CoV-2.
  • |*Antibody-Dependent Enhancement[MESH]
  • |Angiotensin-Converting Enzyme 2/metabolism[MESH]
  • |Antibodies, Neutralizing/immunology[MESH]
  • |Antibodies, Viral/immunology[MESH]
  • |COVID-19/*immunology/*metabolism[MESH]
  • |Cell Line[MESH]
  • |Humans[MESH]
  • |Interleukin-6/*metabolism[MESH]
  • |Myeloid Cells/immunology/metabolism[MESH]
  • |Patients[MESH]
  • |SARS-CoV-2/*immunology[MESH]


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