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10.1016/j.molimm.2021.06.021

http://scihub22266oqcxt.onion/10.1016/j.molimm.2021.06.021
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suck abstract from ncbi


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pmid34242919      Mol+Immunol 2021 ; 137 (ä): 105-113
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  • Untangling COVID-19 and autoimmunity: Identification of plausible targets suggests multi organ involvement #MMPMID34242919
  • Mohkhedkar M; Venigalla SSK; Janakiraman V
  • Mol Immunol 2021[Sep]; 137 (ä): 105-113 PMID34242919show ga
  • Underlying mechanisms of multi-organ manifestations and exacerbated inflammation in COVID-19 are yet to be delineated. The hypothesis of SARS-CoV-2 triggering autoimmunity is gaining attention and, in the present study, we have identified 28 human proteins harbouring regions homologous to SARS-CoV-2 peptides that could possibly be acting as autoantigens in COVID-19 patients displaying autoimmune conditions. Interestingly, these conserved regions are amongst the experimentally validated B cell epitopes of SARS-CoV-2 proteins. The reported human proteins have demonstrated presence of autoantibodies against them in typical autoimmune conditions which may explain the frequent occurrence of autoimmune conditions following SARS-CoV-2 infection. Moreover, the proposed autoantigens' widespread tissue distribution is suggestive of their involvement in multi-organ manifestations via molecular mimicry. We opine that our report may aid in directing subsequent necessary antigen-specific studies, results of which would be of long-term relevance in management of extrapulmonary symptoms of COVID-19.
  • |Autoantibodies/immunology[MESH]
  • |Autoantigens/*immunology[MESH]
  • |Autoimmune Diseases/*complications/immunology/virology[MESH]
  • |Autoimmunity/immunology[MESH]
  • |COVID-19/*etiology/immunology/pathology[MESH]
  • |Epitopes, B-Lymphocyte/*immunology[MESH]
  • |Humans[MESH]
  • |Molecular Mimicry/immunology[MESH]


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