Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/4248
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dc.contributor.authorFlanagan, K. L.en
dc.contributor.authorMacartney, K.en
dc.contributor.authorRussell, F.en
dc.contributor.authorTeh, B. W.en
dc.contributor.authorWen, S. C. H.en
dc.contributor.authorCrawford, N. W.en
dc.contributor.authorBest, E.en
dc.contributor.authorKoirala, A.en
dc.contributor.authorGiles, M.en
dc.date.accessioned2022-11-07T23:50:52Z-
dc.date.available2022-11-07T23:50:52Z-
dc.date.issued2020en
dc.identifier.citation11 , 2020en
dc.identifier.otherRISen
dc.identifier.urihttp://dora.health.qld.gov.au/qldresearchjspui/handle/1/4248-
dc.description.abstractThere are currently around 200 SARS-CoV-2 candidate vaccines in preclinical and clinical trials throughout the world. The various candidates employ a range of vaccine strategies including some novel approaches. Currently, the goal is to prove that they are safe and immunogenic in humans (phase 1/2 studies) with several now advancing into phase 2 and 3 trials to demonstrate efficacy and gather comprehensive data on safety. It is highly likely that many vaccines will be shown to stimulate antibody and T cell responses in healthy individuals and have an acceptable safety profile, but the key will be to confirm that they protect against COVID-19. There is much hope that SARS-CoV-2 vaccines will be rolled out to the entire world to contain the pandemic and avert its most damaging impacts. However, in all likelihood this will initially require a targeted approach toward key vulnerable groups. Collaborative efforts are underway to ensure manufacturing can occur at the unprecedented scale and speed required to immunize billions of people. Ensuring deployment also occurs equitably across the globe will be critical. Careful evaluation and ongoing surveillance for safety will be required to address theoretical concerns regarding immune enhancement seen in previous contexts. Herein, we review the current knowledge about the immune response to this novel virus as it pertains to the design of effective and safe SARS-CoV-2 vaccines and the range of novel and established approaches to vaccine development being taken. We provide details of some of the frontrunner vaccines and discuss potential issues including adverse effects, scale-up and delivery.L6331147862020-10-26 <br />2020-11-26 <br />en
dc.language.isoenen
dc.relation.ispartofFrontiers in Immunologyen
dc.titleProgress and Pitfalls in the Quest for Effective SARS-CoV-2 (COVID-19) Vaccinesen
dc.typeArticleen
dc.identifier.doi10.3389/fimmu.2020.579250en
dc.subject.keywordstumor necrosis factoren
dc.subject.keywordsvirulence factoren
dc.subject.keywordsvirus vaccineen
dc.subject.keywordsvirus vectoren
dc.subject.keywordsvitronectinen
dc.subject.keywordsantigen presenting cellen
dc.subject.keywordsBCG vaccinationen
dc.subject.keywordsbioinformaticsen
dc.subject.keywordsCD4+ T lymphocyteen
dc.subject.keywordsCD8+ T lymphocyteen
dc.subject.keywordscell infiltrationen
dc.subject.keywordscoronavirus disease 2019en
dc.subject.keywordsdendritic cellen
dc.subject.keywordsdisease severityen
dc.subject.keywordsenzyme linked immunosorbent assayen
dc.subject.keywordsgastrointestinal diseaseen
dc.subject.keywordsgene expressionen
dc.subject.keywordshospitalizationen
dc.subject.keywordshumanen
dc.subject.keywordsHuman respiratory syncytial virusen
dc.subject.keywordshypersensitivityen
dc.subject.keywordsimmune responseen
dc.subject.keywordsimmunizationen
dc.subject.keywordsimmunogenicityen
dc.subject.keywordsimmunopathologyen
dc.subject.keywordsimmunosuppressive treatmenten
dc.subject.keywordsinnate immunityen
dc.subject.keywordsnonhumanen
dc.subject.keywordsphagocytosisen
dc.subject.keywordsphase 1 clinical trial (topic)en
dc.subject.keywordsregulatory T lymphocyteen
dc.subject.keywordsreviewen
dc.subject.keywordsRNA-binding domainen
dc.subject.keywordsTh1 cellen
dc.subject.keywordsTh2 cellen
dc.subject.keywordstrainingen
dc.subject.keywordsvaccine immunogenicityen
dc.subject.keywordsvirus particleen
dc.subject.keywordstissue injuryen
dc.subject.keywordsangiotensin converting enzyme 2DNA vaccineen
dc.subject.keywordsgamma interferonen
dc.subject.keywordsglycoproteinen
dc.subject.keywordsgranulocyte colony stimulating factoren
dc.subject.keywordsinterferon induced helicase C domain containing protein 1en
dc.subject.keywordsinterleukin 13en
dc.subject.keywordsinterleukin 17en
dc.subject.keywordsinterleukin 2en
dc.subject.keywordsinterleukin 4en
dc.subject.keywordsinterleukin 6en
dc.subject.keywordsinterleukin 7en
dc.subject.keywordslentivirus vectoren
dc.subject.keywordsliposomeen
dc.subject.keywordsmalaria vaccineen
dc.subject.keywordsnanoparticleen
dc.subject.keywordsneutralizing antibodyen
dc.subject.keywordspattern recognition receptoren
dc.subject.keywordspeptide vaccineen
dc.subject.keywordsretinoic aciden
dc.subject.keywordstoll like receptoren
dc.subject.keywordstoll like receptor 4en
dc.relation.urlhttps://www.embase.com/search/results?subaction=viewrecord&id=L633114786&from=exporthttp://dx.doi.org/10.3389/fimmu.2020.579250 |en
dc.identifier.risid2806en
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.languageiso639-1en-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairetypeArticle-
Appears in Sites:Children's Health Queensland Publications
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