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10.1002/jmv.26009

http://scihub22266oqcxt.onion/10.1002/jmv.26009
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32410266!7272823!32410266
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suck abstract from ncbi


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pmid32410266      J+Med+Virol 2020 ; 92 (9): 1495-1500
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  • Immunoregulation with mTOR inhibitors to prevent COVID-19 severity: A novel intervention strategy beyond vaccines and specific antiviral medicines #MMPMID32410266
  • Zheng Y; Li R; Liu S
  • J Med Virol 2020[Sep]; 92 (9): 1495-1500 PMID32410266show ga
  • Coronavirus disease 2019 (COVID-19) has become a major global public health concern. The mortality rate for critically ill patients is up to 60%, and, thus, reducing the disease severity and case mortality is a top priority. Currently, cytokine storms are considered as the major cause of critical illness and death due to COVID-19. After a systematical review of the literature, we propose that cross-reactive antibodies associated with antibody-dependent enhancement (ADE) may actually be the cause of cytokine storms. It would be more difficult to develop vaccines for highly pathogenic human coronaviruses (CoVs) if ADE characteristics are taken into consideration. Therefore, it is urgent to find an effective way to prevent the occurrence of severe illness as severe acute respiratory syndrome CoV-2 specific drugs or vaccines are still in development. If the activation of memory B cells can be selectively inhibited in high-risk patients at an early stage of COVID-19 to reduce the production of cross-reactive antibodies against the virus, we speculate that ADE can be circumvented and severe symptoms can be prevented. The mammalian target of rapamycin (mTOR) inhibitors satisfy such needs and it is recommended to conduct clinical trials for mTOR inhibitors in preventing the severity of COVID-19.
  • |*Antibody-Dependent Enhancement[MESH]
  • |*COVID-19 Drug Treatment[MESH]
  • |*Immunomodulation[MESH]
  • |Antibodies, Viral/immunology[MESH]
  • |B-Lymphocytes/drug effects[MESH]
  • |Cross Reactions[MESH]
  • |Cytokine Release Syndrome/virology[MESH]
  • |Humans[MESH]


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