key: cord-1050554-wt6azxc1
authors: McIntyre, Peter; Joo, Ye Jin; Chiu, Clayton; Flanagan, Katie; Macartney, Kristine
title: COVID-19 vaccines – are we there yet?
date: 2020-12-17
journal: Aust Prescr
DOI: 10.18773/austprescr.2020.084
sha: 08012f54a9b5da5a9a51240cf9da53b9d00ff20f
doc_id: 1050554
cord_uid: wt6azxc1

The novel coronavirus SARS-CoV-2, the cause of the COVID-19 pandemic, is a highly infectious human respiratory pathogen to which the global population had no prior immunity. The virus will likely continue to cause significant morbidity until there is a broadly effective vaccine As of mid-December 2020, more than 200 COVID-19 vaccine candidates are in development and 11 have entered phase III clinical trials globally. All generate immunity to the viral spike glycoprotein Three vaccine candidates have agreements for procurement and use in Australia if efficacy and safety requirements are met – one protein-based vaccine, one vaccine using a simian-derived adenovirus vector and one messenger RNA vaccine. The latter two vaccines have published interim analyses and efficacy results of their phase III trials. The messenger RNA vaccine is being rolled out in the UK, USA and Canada Significant uncertainties remain. How well will some of those at highest risk of severe disease (such as older people aged >75 years and those with immunocompromising conditions) be protected by a vaccine, and for how long? Also, to what extent will vaccination protect against infection? This will determine the degree of indirect ‘herd’ protection needed through broad vaccine coverage of younger age groups

Like influenza, coronaviruses are RNA viruses. The SARS-CoV-2 virus which causes COVID-19 belongs to the betacoronavirus family. This also includes the SARS-CoV-1 virus which causes Severe Acute Respiratory Syndrome (SARS) and MERS-CoV which causes Middle East Respiratory Syndrome (MERS). Another four seasonal human coronaviruses circulate annually, mostly causing mild upper respiratory tract infections. SARS (2003) and MERS (2014) caused short-lived epidemics with a high case fatality. MERS still occurs sporadically, but SARS-CoV-1 has not been in circulation since 2008. 1 COVID-19 is most severe in the elderly and those with significant comorbidities. SARS-CoV-2 also results in asymptomatic infection. Unlike SARS-CoV-1, SARS-CoV-2 can be very contagious before and shortly after symptom onset, which has helped drive rapid global spread. Although estimates of the degree of immunity in the population required to control the COVID-19 pandemic vary, most centre around 60-70%. 2 High coverage with effective vaccines is the only ethically acceptable path to achieving this level of immunity. The effectiveness of the various COVID-19 vaccine candidates will depend on their ability to reduce infectiousness versus their ability to prevent serious disease if someone gets infected.

Full text free online at nps.org.au/australian-prescriber VOLUME 44 : NUMBER 1 : FEBRUARY 2021 Progress through all trial stages usually takes at least 10 years. However, the magnitude of the COVID-19 pandemic has led to funding for the development of 'vaccines at pandemic speed' by running some processes in parallel (see Fig. 1 ). 4 Many studies have combined phase I and II trials and a few have combined phase II and III trials to compress time frames. This has not compromised scientific rigour as safety, immunogenicity and efficacy outcomes are strictly assessed and safety monitoring will continue even after registration.

As of mid-December 2020, four COVID-19 vaccines have reported estimates of efficacy from their phase III trials in press releases. 6 However, only two of these, one adenovirus-vectored vaccine (University of Oxford/AstraZeneca) and one messenger RNA vaccine (BioNTech/Pfizer), have published interim efficacy results. 7, 8 Although vaccines produced in China and Russia have been approved for use in those countries (Table 1) , detailed efficacy and safety data at the level required by regulatory bodies in most countries, including Australia, are not currently publicly accessible.

COVID-19 vaccine candidates have been developed using conventional and novel approaches to vaccine development (see Fig. 2 ). All of them generate immunity to the viral spike glycoprotein, which is required for the virus to enter host cells. The aim of vaccine-generated antibodies against the spike glycoprotein is to prevent viral replication, or 'neutralise' the virus, and stop it from infecting cells.

Conventional approaches to vaccine development have the advantage of being familiar and well-studied, but these vaccines may take longer to manufacture. COVID-19 vaccine candidates developed by conventional approaches and currently in clinical trials include:

• inactivated viral vaccines (like the influenza (split virus) and inactivated polio (whole virus) vaccines)

• protein or protein subunit vaccines (like the diphtheria and tetanus protein (toxoid) vaccines, hepatitis B and herpes zoster adjuvanted vaccine)

• virus-like particles (like the human papillomavirus vaccine)

• live-attenuated viral vaccines

Only one live-attenuated COVID-19 vaccine is currently being progressed to human studies (NCT04619628).

Novel approaches have potential advantages in the strength of immune responses and rapidity of manufacture but are less well studied. These newer technologies for COVID-19 include viral vectored vaccines and mRNA and DNA vaccines. Vectored vaccines currently in phase III trial use adenoviruses of human or non-human primate origin. These are harmless, non-replicating viruses which are able to enter cells and deliver the genetic code for SARS-CoV-2 spike protein antigen. DNA-based vaccines may require specific devices to deliver the DNA into cells (e.g. by electroporation), and from the cytoplasm to the nucleus once in the cell. Conversely, mRNA vaccines are often encapsulated into lipid nanoparticles which allow mRNA to fuse into the cytoplasm without being degraded (Moderna and BioNTech/Pfizer's vaccines use this technology). Both DNA and mRNA vaccines induce the recipient's own cells to produce SARS-CoV-2 spike protein. Table 1 lists the characteristics of the 11 vaccine candidates in phase III trials as of mid-December 2020. 7-17 Table 2 lists vaccines in phase I or II trials in Australia.

Australia currently has one agreement to locally manufacture a vaccine -ChAdOx1 nCoV-19/AZD1222 (University of Oxford/AstraZeneca). This is a viral vectored vaccine in phase III trials, with interim efficacy results. 7 Previously the University of Queensland/CSL had an agreement for local manufacture of the v451 clamp vaccine. However a decision has been made to not proceed into phase III clinical trials as antibodies to the vaccine interfere with HIV screening tests. 18, 19 Vaccine registration

All COVID-19 vaccines used in Australia will require approval by the Therapeutic Goods Administration (TGA). The TGA has recently determined that three vaccines in phase III trials are eligible to apply for provisional registration in the Australian Register of Therapeutic Goods. These are:

• BNT162b2 (mRNA vaccine)

Provisional TGA registration of medicines or vaccines is on the basis of preliminary clinical data on quality, safety and effectiveness of the vaccine, and the sponsor's plan to submit comprehensive clinical and stability data before the provisional registration ends. 20 The status of other vaccine candidates is available through the World Health Organization website which is regularly updated. 21 As of mid-December, the BNT162b2 vaccine has been granted Emergency Use Authorisation in at least three countries, including the UK, Canada and the USA, where it is being rolled out in COVID-19 vaccination programs.

Full text free online at nps.org.au/australian-prescriber 

Safety is paramount at all stages of the clinical development process. It is built into vaccine development by guidelines from the earliest stages (Good Laboratory Practice) to clinical trials (Good Clinical Practice). For each vaccine, safety is assessed by Data Safety Monitoring Boards, independent of the manufacturer, during the trial. Safety is also assessed after trial completion by the regulator when it reviews the vaccine for approval. 22 In Australia, enhanced reporting of adverse events following immunisation (AEFI) at national and state and territory levels is designed to ensure that the safety of any COVID-19 vaccines used in the National Immunisation Program is comprehensively monitored. This is supplemented by near real-time active vaccine safety surveillance, such as through AusVaxSafety. 23 All these mechanisms will be outlined in detail in the Australian national COVID-19 vaccine pharmacovigilance plan.

Some potential safety concerns were identified early on for COVID-19 vaccine candidates based on previous experience with coronavirus vaccine candidates. In experimental animals given vaccines for SARS and MERS, some studies showed evidence of lung immunopathology after challenge with wild virus (termed disease enhancement). 24 However, this proved not to be an issue for COVID-19

Full text free online at nps.org.au/australian-prescriber vaccines in animal studies, as high concentrations of neutralising antibody were produced. These antibodies not only bind to viral antigen, they also prevent the virus from infecting cells. In addition, the T-cell responses seen were not associated with allergy (i.e. T helper 1 biased rather than T helper 2). 24 It is a requirement that vaccine candidates satisfy these criteria before entering phase I human trials.

To date, no COVID-19 candidate vaccines have generated safety signals of concern.

How will we use COVID-19 vaccines?

There is general agreement that front-line workers, such as healthcare staff, and individuals at the highest risk of severe disease, particularly the elderly, should be prioritised to receive COVID-19 vaccines once available. [25] [26] [27] A key question is how well vaccines that show protection in young, healthy individuals will work in people who have chronic medical conditions or are immunocompromised, and in older people, particularly those who are frail or living in residential care. Up until 2020, the only vaccine with high levels of protection in older people (>70 years) is a recombinant shingles vaccine which uses a novel adjuvant. 28 This vaccine is available in the USA, but not Australia. Such novel adjuvants may prove important for COVID-19 vaccines in older people and other groups likely to have reduced vaccine responses. Another key uncertainty is whether COVID-19 vaccination will reduce transmission of SARS-CoV-2 and produce indirect 'herd' immunity which could protect people who are unable to respond to vaccines. It will take time for data to emerge on this and on the duration of protection and need for repeated doses. 29 More detailed priorities for specific target groups will vary with the availability of vaccines and their specific characteristics. Vaccine recommendations, along with other control recommendations are evolving as our experience with COVID-19 grows.

Ensuring public confidence in both the safety and effectiveness of COVID-19 vaccines will be critical to achieving high vaccine uptake among target populations during vaccine roll out in Australia from 2021. 30 As COVID-19 vaccines become available for use, immunisation service providers can take early steps to prepare for vaccine introduction, such as ensuring connectivity to the Australian Immunisation Register and engagement with other systems such as adverse events following immunisation reporting.

Much needs to be done to ensure that the unprecedented scientific effort which has allowed rapid development of COVID-19 vaccines translates into the high vaccine uptake needed to rapidly overcome the most significant global pandemic seen in over a century.

Comparing SARS-CoV-2 with SARS-CoV and influenza pandemics

The false promise of herd immunity

Developing Covid-19 vaccines at pandemic speed

National Vaccine Advisory Committee. Lessons learned from a review of the development of selected vaccines

New York Times COVID vaccine tracker

Oxford COVID Vaccine Trial Group. Safety and efficacy of the ChAdOx1 nCoV-19 vaccine (AZD1222) against SARS-CoV-2: an interim analysis of four randomised controlled trials in Brazil, South Africa, and the UK

C4591001 Clinical Trial Group. Safety and efficacy of the BNT162b2 mRNA Covid-19 vaccine

Oxford COVID Vaccine Trial Group. Safety and immunogenicity of the ChAdOx1 nCoV-19 vaccine against SARS-CoV2: a preliminary report of a phase 1/2, singleblind, randomised controlled trial

Safety and immunogenicity of ChAdOx1 nCoV-19 vaccine administered in a prime-boost regimen in young and old adults (COV002): a single-blind, randomised, controlled, phase 2/3 trial

mRNA-1273 Study Group. An mRNA Vaccine against SARS-CoV-2 -Preliminary Report

mRNA-1273 Study Group. Safety and immunogenicity of SARS-CoV-2 mRNA-1273 vaccine in older adults

Safety and immunogenicity of two RNA-based Covid-19 vaccine candidates

Safety and immunogenicity of an rAd26 and rAd5 vector-based heterologous prime-boost COVID-19 vaccine in two formulations: two open, non-randomised phase 1/2 studies from Russia

Immunogenicity and safety of a recombinant adenovirus type-5-vectored COVID-19 vaccine in healthy adults aged 18 years or older: a randomised, double-blind, placebocontrolled, phase 2 trial

Safety, tolerability, and immunogenicity of a recombinant adenovirus type-5 vectored COVID-19 vaccine: a doseescalation, open-label, non-randomised, first-in-human trial

Phase 1-2 Trial of a SARS-CoV-2 recombinant spike protein nanoparticle vaccine

Australia secures 20 million extra Astra Zeneca vaccines

Update on UQ COVID-19 vaccine

Therapeutic Goods Administration. COVID-19 vaccine approval process

World Health Organization. Draft landscape of COVID-19 candidate vaccines

REFERENCES COVID-19 vaccines -are we there yet? ARTICLE Full text free online at nps.org.au/australian-prescriber VOLUME

Australian Government Department of Health. Vaccine safety

AusVaxSafety surveillance team. Real-time safety surveillance of seasonal influenza vaccines in children

Consensus summary report for CEPI/BC March 12-13, 2020 meeting: Assessment of risk of disease enhancement with COVID-19 vaccines

Fairly prioritizing groups for access to COVID-19 vaccines

The National Academies of Sciences Engineering Medicine. A framework for equitable allocation of vaccine for the novel coronavirus

ZOE-70 Study Group. Efficacy of the herpes zoster subunit vaccine in adults 70 years of age or older

Progress and pitfalls in the quest for effective SARS-CoV-2 (COVID-19) vaccines frontiers in immunology

Preparing the public for COVID-19 vaccines: how can general practitioners build vaccine confidence and optimise uptake for themselves and their patients?

Testing for COVID-19