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10.1186/s10020-021-00313-3

http://scihub22266oqcxt.onion/10.1186/s10020-021-00313-3
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34022793!8140578!34022793
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suck abstract from ncbi


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pmid34022793      Mol+Med 2021 ; 27 (1): 49
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  • Possible inhibition of GM-CSF production by SARS-CoV-2 spike-based vaccines #MMPMID34022793
  • Li J; Wang P; Tracey KJ; Wang H
  • Mol Med 2021[May]; 27 (1): 49 PMID34022793show ga
  • A SARS-like coronavirus 2 (SARS-CoV-2) has caused a pandemic Coronavirus Disease 2019 (COVID-19) that killed more than 3.3 million people worldwide. Like the SARS-CoV, SARS-CoV-2 also employs a receptor-binding motif (RBM) of its spike protein to bind a host receptor, the angiotensin-converting enzyme 2 (ACE2), to gain entry. Currently, several mRNA or adenoviral vaccines encoding for the spike protein of SARS-CoV-2 are being used to boost antibodies capable of inhibiting spike-ACE2 interaction and viral entry. However, recent evidence has also suggested an anti-inflammatory effect of spike-reactive antibodies, suggesting that some SARS-CoV-2 spike-based vaccines may elicit protective antibodies capable of inhibiting GM-CSF production and COVID-19 progression.
  • |Angiotensin-Converting Enzyme 2/*metabolism[MESH]
  • |Antibodies, Neutralizing/immunology/*metabolism[MESH]
  • |COVID-19 Vaccines/immunology/*therapeutic use[MESH]
  • |COVID-19/metabolism/*prevention & control/virology[MESH]
  • |Granulocyte-Macrophage Colony-Stimulating Factor/*antagonists & inhibitors/metabolism[MESH]
  • |Host-Pathogen Interactions/drug effects[MESH]
  • |Humans[MESH]
  • |Protein Binding/drug effects[MESH]
  • |SARS-CoV-2/immunology/metabolism/physiology[MESH]
  • |Spike Glycoprotein, Coronavirus/immunology/*metabolism[MESH]
  • |Virus Internalization/drug effects[MESH]


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