Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/24836
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dc.contributor.authorCopaescu, Ana-
dc.contributor.authorSmibert, Olivia C-
dc.contributor.authorGibson, Andrew-
dc.contributor.authorPhillips, Elizabeth J-
dc.contributor.authorTrubiano, Jason-
dc.date2020-09-
dc.date.accessioned2020-09-28T23:22:12Z-
dc.date.available2020-09-28T23:22:12Z-
dc.date.issued2020-09-
dc.identifier.citationThe Journal of Allergy and Clinical Immunology 2020; 146(3): 518-534.e1en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/24836-
dc.description.abstractThe coronavirus disease 2019 pandemic caused by severe acute respiratory syndrome coronavirus 2 presents with a spectrum of clinical manifestations from asymptomatic or mild, self-limited constitutional symptoms to a hyperinflammatory state ("cytokine storm") followed by acute respiratory distress syndrome and death. The objective of this study was to provide an evidence-based review of the associated pathways and potential treatment of the hyperinflammatory state associated with severe acute respiratory syndrome coronavirus 2 infection. Dysregulated immune responses have been reported to occur in a smaller subset of those infected with severe acute respiratory syndrome coronavirus 2, leading to clinical deterioration 7 to 10 days after initial presentation. A hyperinflammatory state referred to as cytokine storm in its severest form has been marked by elevation of IL-6, IL-10, TNF-α, and other cytokines and severe CD4+ and CD8+ T-cell lymphopenia and coagulopathy. Recognition of at-risk patients could permit early institution of aggressive intensive care and antiviral and immune treatment to reduce the complications related to this proinflammatory state. Several reports and ongoing clinical trials provide hope that available immunomodulatory therapies could have therapeutic potential in these severe cases. This review highlights our current state of knowledge of immune mechanisms and targeted immunomodulatory treatment options for the current coronavirus disease 2019 pandemic.en
dc.language.isoeng-
dc.subjectCOVID-19en
dc.subjectIL-6en
dc.subjectJAKen
dc.subjectSARS-CoV-2en
dc.subjectSTINGen
dc.subjectTNF-αen
dc.subjectcytokine stormen
dc.subjectcytokinesen
dc.subjecthemophagocytic lymphohistiocytosisen
dc.subjecthyperinflammatoryen
dc.subjectproinflammatoryen
dc.subjectsepsisen
dc.titleThe role of IL-6 and other mediators in the cytokine storm associated with SARS-CoV-2 infection.en
dc.typeJournal Articleen
dc.identifier.journaltitleThe Journal of Allergy and Clinical Immunologyen
dc.identifier.affiliationCentre for Antibiotic Allergy and Researchen
dc.identifier.affiliationInfectious Diseasesen
dc.identifier.affiliationInstitute for Immunology and Infectious Diseases, Murdoch University, Murdoch, Australiaen
dc.identifier.affiliationDepartment of Infectious Diseases, Vanderbilt University Medical Centre, Nashville, Tenn, USAen
dc.identifier.affiliationDepartment of Oncology, Sir Peter MacCallum Cancer Centre, The University of Melbourne, Parkville, Australiaen
dc.identifier.affiliationNational Centre for Infections in Cancer, Peter MacCallum Cancer Centre, Parkville, Australiaen
dc.identifier.affiliationMedicine (University of Melbourne)en
dc.identifier.doi10.1016/j.jaci.2020.07.001en
dc.type.contentTexten
dc.identifier.pubmedid32896310-
local.name.researcherCopaescu, Ana-
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptInfectious Diseases-
crisitem.author.deptInfectious Diseases-
crisitem.author.deptInfectious Diseases-
crisitem.author.deptMedicine (University of Melbourne)-
crisitem.author.deptCentre for Antibiotic Allergy and Research-
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