Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/4248
Title: Progress and Pitfalls in the Quest for Effective SARS-CoV-2 (COVID-19) Vaccines
Authors: Flanagan, K. L.
Macartney, K.
Russell, F.
Teh, B. W.
Wen, S. C. H.
Crawford, N. W.
Best, E.
Koirala, A.
Giles, M.
Issue Date: 2020
Source: 11 , 2020
Journal: Frontiers in Immunology
Abstract: There 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
2020-11-26
DOI: 10.3389/fimmu.2020.579250
Resources: https://www.embase.com/search/results?subaction=viewrecord&id=L633114786&from=exporthttp://dx.doi.org/10.3389/fimmu.2020.579250 |
Keywords: tumor necrosis factor;virulence factor;virus vaccine;virus vector;vitronectin;antigen presenting cell;BCG vaccination;bioinformatics;CD4+ T lymphocyte;CD8+ T lymphocyte;cell infiltration;coronavirus disease 2019;dendritic cell;disease severity;enzyme linked immunosorbent assay;gastrointestinal disease;gene expression;hospitalization;human;Human respiratory syncytial virus;hypersensitivity;immune response;immunization;immunogenicity;immunopathology;immunosuppressive treatment;innate immunity;nonhuman;phagocytosis;phase 1 clinical trial (topic);regulatory T lymphocyte;review;RNA-binding domain;Th1 cell;Th2 cell;training;vaccine immunogenicity;virus particle;tissue injury;angiotensin converting enzyme 2DNA vaccine;gamma interferon;glycoprotein;granulocyte colony stimulating factor;interferon induced helicase C domain containing protein 1;interleukin 13;interleukin 17;interleukin 2;interleukin 4;interleukin 6;interleukin 7;lentivirus vector;liposome;malaria vaccine;nanoparticle;neutralizing antibody;pattern recognition receptor;peptide vaccine;retinoic acid;toll like receptor;toll like receptor 4
Type: Article
Appears in Sites:Children's Health Queensland Publications

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