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10.1080/14712598.2020.1798399

http://scihub22266oqcxt.onion/10.1080/14712598.2020.1798399
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32700604!ä!32700604

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suck abstract from ncbi


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pmid32700604      Expert+Opin+Biol+Ther 2020 ; 20 (9): 1025-1031
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  • Itolizumab, an anti-CD6 monoclonal antibody, as a potential treatment for COVID-19 complications #MMPMID32700604
  • Loganathan S; Athalye SN; Joshi SR
  • Expert Opin Biol Ther 2020[Sep]; 20 (9): 1025-1031 PMID32700604show ga
  • INTRODUCTION: The globally rampant SARS CoV-2 pandemic requires novel medical strategies to control the severity of disease and death due to complications. Of the 15-20% patients that develop pulmonary symptoms, a sub-set develops an acute respiratory distress syndrome (ARDS) rapidly progressing into a critical condition. Marked elevation of cytokines/chemokines is observed with elevation of additional markers of inflammation, coagulation, and organ damage such as CRP, D-dimer, LDH, Ferritin and Troponin-I. This hyperinflammation leads to worsening of oxygen saturation due to pulmonary infiltration and exudation, organ damage, and dysfunction of coagulation pathway and may lead to multi-organ failure. AREAS COVERED: The role of anti-inflammatory monoclonal antibodies such as Itolizumab, in cytokine storm. EXPERT OPINION: Itolizumab, an anti-CD6 humanized IgG1 mAb, binds to domain-1 of CD-6 that is responsible for priming, activation, and differentiation of T-cells. Itolizumab significantly reduces T-cell proliferation along with substantial downregulation of the production of cytokines/chemokines. Approved for moderate to severe chronic plaque psoriasis in 2013 it is currently being studied for addressing COVID-19 related cytokine storm and its complications. This article reviews its use in COVID-19 infections; its dose, administration protocol, contra-indications, and safety in treating moderate-to-severe ARDS by preventing and treating the cytokine storm and its complications.
  • |*Betacoronavirus[MESH]
  • |Antibodies, Monoclonal, Humanized/pharmacology/*therapeutic use[MESH]
  • |Antigens, CD/*immunology[MESH]
  • |Antigens, Differentiation, T-Lymphocyte/*immunology[MESH]
  • |COVID-19[MESH]
  • |Cell Differentiation/drug effects/physiology[MESH]
  • |Cell Proliferation/drug effects/physiology[MESH]
  • |Coronavirus Infections/*drug therapy/*immunology[MESH]
  • |Cytokines/antagonists & inhibitors/immunology[MESH]
  • |Humans[MESH]
  • |Lymphocyte Activation/drug effects/physiology[MESH]
  • |Pandemics[MESH]
  • |Pneumonia, Viral/*drug therapy/*immunology[MESH]
  • |SARS-CoV-2[MESH]
  • |T-Lymphocytes/drug effects/immunology[MESH]


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