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10.1007/s12192-020-01148-3

http://scihub22266oqcxt.onion/10.1007/s12192-020-01148-3
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suck abstract from ncbi


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pmid32754823      Cell+Stress+Chaperones 2020 ; 25 (5): 737-741
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  • Human molecular chaperones share with SARS-CoV-2 antigenic epitopes potentially capable of eliciting autoimmunity against endothelial cells: possible role of molecular mimicry in COVID-19 #MMPMID32754823
  • Marino Gammazza A; Legare S; Lo Bosco G; Fucarino A; Angileri F; Conway de Macario E; Macario AJ; Cappello F
  • Cell Stress Chaperones 2020[Sep]; 25 (5): 737-741 PMID32754823show ga
  • Severe acute respiratory syndrome corona virus 2 (SARS-CoV-2), the cause of COVID-19 disease, has the potential to elicit autoimmunity because mimicry of human molecular chaperones by viral proteins. We compared viral proteins with human molecular chaperones, many of which are heat shock proteins, to determine if they share amino acid-sequence segments with immunogenic-antigenic potential, which can elicit cross-reactive antibodies and effector immune cells with the capacity to damage-destroy human cells by a mechanism of autoimmunity. We identified the chaperones that can putatively participate in molecular mimicry phenomena after SARS-CoV-2 infection, focusing on those for which endothelial cell plasma-cell membrane localization has already been demonstrated. We also postulate that post-translational modifications, induced by physical (shear) and chemical (metabolic) stress caused respectively by the risk factors hypertension and diabetes, might have a role in determining plasma-cell membrane localization and, in turn, autoimmune-induced endothelial damage.
  • |*Heat-Shock Proteins/chemistry/immunology[MESH]
  • |*Viral Proteins/chemistry/immunology[MESH]
  • |Amino Acid Sequence[MESH]
  • |Autoantigens[MESH]
  • |Autoimmunity[MESH]
  • |Betacoronavirus/*metabolism[MESH]
  • |COVID-19[MESH]
  • |Coronavirus Infections/*virology[MESH]
  • |Databases, Protein[MESH]
  • |Endothelial Cells/metabolism[MESH]
  • |Humans[MESH]
  • |Immunodominant Epitopes[MESH]
  • |Molecular Mimicry[MESH]
  • |Pandemics[MESH]
  • |Pneumonia, Viral/*virology[MESH]


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