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10.1016/j.humimm.2021.06.011

http://scihub22266oqcxt.onion/10.1016/j.humimm.2021.06.011
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34229864!8245343!34229864
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suck abstract from ncbi


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pmid34229864      Hum+Immunol 2021 ; 82 (10): 733-745
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  • Humoral immune mechanisms involved in protective and pathological immunity during COVID-19 #MMPMID34229864
  • Widjaja G; Turki Jalil A; Sulaiman Rahman H; Abdelbasset WK; Bokov DO; Suksatan W; Ghaebi M; Marofi F; Gholizadeh Navashenaq J; Jadidi-Niaragh F; Ahmadi M
  • Hum Immunol 2021[Oct]; 82 (10): 733-745 PMID34229864show ga
  • The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causing COVID-19 is associated with excessive inflammation, as a main reason for severe condition and death. Increased inflammatory cytokines and humoral response to SARS-CoV-2 correlate with COVID-19 immunity and pathogenesis. Importantly, the levels of pro-inflammatory cytokines that increase profoundly in systemic circulation appear as part of the clinical pictures of two overlapping conditions, sepsis and the hemophagocytic syndromes. Both conditions can develop lethal inflammatory responses that lead to tissue damage, however, in many patients hemophagocytic lymphohistiocytosis (HLH) can be differentiated from sepsis. This is a key issue because the life-saving aggressive immunosuppressive treatment, required in the HLH therapy, is absent in sepsis guidelines. This paper aims to describe the pathophysiology and clinical relevance of these distinct entities in the course of COVID-19 that resemble sepsis and further highlights two effector arms of the humoral immune response (inflammatory cytokine and immunoglobulin production) during COVID-19 infection.
  • |Animals[MESH]
  • |COVID-19/*immunology[MESH]
  • |Cytokines/immunology[MESH]
  • |Humans[MESH]
  • |Immunity, Humoral/*immunology[MESH]
  • |Inflammation/immunology[MESH]
  • |Lymphohistiocytosis, Hemophagocytic/immunology[MESH]
  • |SARS-CoV-2/immunology[MESH]


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