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      COVID-19 spread in the UK: the end of the beginning?

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          Abstract

          As the UK Government response to the COVID-19 pandemic reaches the end of its first phase, there are opportunities to be taken and challenges to be met. Specific opportunities include improving data collection and management, and putting in place as quickly as possible an effective test, trace, and isolate system for the UK. These are of immediate and high priority. The challenges include the development of high-level expertise within the newly established Joint Biosecurity Centre, a UK Government body. 1 The Joint Biosecurity Centre will take over some of the responsibilities of the UK Science Advisory Group for Emergencies (SAGE) in advising policy makers how best to control COVID-19. Ideally, the Joint Biosecurity Centre should be an informed body that distils knowledge for policy formulation, rather than a creator of that knowledge. In the UK, lockdown measures were put in place some weeks too late to alleviate the rapid spread of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). For all epidemics, the earlier the measures are put in place to restrict transmission, the smaller the total size of the epidemic and the concomitant morbidity and mortality. By the end of April, 2020, the COVID-19 epidemic in the UK showed signs of suppression as daily reports of cases began to enter a slow decline. The UK Government's delay in implementing physical distancing measures centred on how long the population would tolerate strict lockdown measures and on an ill-defined and dangerous notion of the creation of herd immunity by natural infection. This delay resulted in the UK having one of the largest epidemics of any country at this stage of the pandemic, when judged both by cases per head of population and mortality per case of infection. 2 The last few weeks have seen the relaxation of UK lockdown measures, but with guidance on sustaining many physical distancing precautions. There remained some uncertainty about the use of face masks in public spaces, 3 until their use was mandated on transport and in other settings in England. As of July 30, 2020, many small outbreaks of COVID-19 remain throughout the UK. Government priorities have understandably been on managing a high burden of COVID-19 morbidity and mortality, but there is now an increasing focus on trying to revitalise the economy and create more social freedoms, given the devastating impacts of lockdown measures. However, this is a strategy fraught with danger. The apparent changes in people's behaviour triggered by a relaxation of the lockdown measures suggest there could be a resurgence in COVID-19 cases sooner than the expected rise later this year. 4 The next weeks will be crucial in judging if there will be a second wave in August and September, 2020. In many countries where lockdown measures were relaxed early, such as the USA, parts of Australia, and some countries in western mainland Europe, resurgence of cases has been recorded. 2 Informative data on epidemics derive from longitudinal (over time) cohort-based (following the same individuals) studies of seroprevalence of past infections and the incidence of new infections, stratified by age, gender, ethnicity, occupation, pre-existing health conditions, spatial home and work or school locations, and clinical outcomes. The UK needs to expand collection of these data and to continue to review the sensitivity and specificity of the available COVID-19 diagnostic tests. The Office for National Statistics (ONS) has developed a COVID-19 infection survey that delivers population-weighted estimates of incidence by region and age. The survey data, together with the blood donor testing database, have provided important insights. Research-based studies such as the Real-time Assessment of Community Transmission (REACT) study are ongoing, but their scale is limited and aims somewhat narrow at present.5, 6 The creation of a large national cohort study should be a priority in the UK to provide information on many facets of the epidemic including immunity after recovery (both antibody and T-cell mediated) and duration of immunity. There have been many problems in the UK on COVID-19-related data quality and access, not all of which have been resolved. Uneven quality and slow access to information on COVID-19 spread and impact, collected by different government organisations, such as the Department of Health and Social Care, Public Health England, and NHS Trusts, have been major impediments to epidemiological analysis of the state of the epidemic and predictions of future trends (Anderson RM, Vegvari C, Baggaley RF, Hollingsworth TD, Maddren R, unpublished). Good practice has been set by the ONS in reporting deaths, and progress is beginning on a single government web portal, which is in a trial format at present, for access to case numbers from various sources. 7 An authoritative body should acquire timely and relevant data at scale across government bodies and distribute it openly to researchers and the public through a well curated portal. Careful thought should be given to how a national database is effectively fed by local public health bodies, and how in return this national information portal feeds back to facilitate local action. Strengthening local public health capacity should be a priority in achieving this goal. What should be measured to give some advanced warning of a resurgence in COVID-19 case numbers in the UK, and how reliable are such measures given existing data sources? The UK Government's advisory group, SAGE, has broadened the information they release to include the effective reproduction number, R t, which describes the average number of secondary cases generated by primary cases at time t, and the epidemic growth rate, r t, which describes the rate of change in case numbers over a defined time.8, 9 The value of r t is easier to estimate using simple statistical methods on changes in incidence over time. If negative in value, the epidemic is contracting. R t is a more informative epidemiological measure (R t <1 is the goal for stopping transmission over a long decay phase), although measurement requires assumptions to be made about other epidemiological parameters, such as the generation time of SARS-CoV-2 (average time from infection to passing the virus on to secondary cases) that can change over the course of the epidemic. Sources of data for the estimation of R t and r t and how they change over time, include reported case numbers, serological surveys, data from contact tracing, and COVID-19 deaths. The specificity and sensitivity of the PCR tests for detecting active viral infection and the serological tests for detecting the presence of antibodies are key for interpreting data. Continued assessment of the accuracy for all tests in use in the UK is essential because of genetic heterogeneity in the SARS-CoV-2 genome at sites that might form the target of the PCR amplification process, and the period over which neutralising and other antibodies to viral antigens can be detected.10, 11, 12 There would be greater clarity on these issues if it was made compulsory for commercial companies that manufacture these tests to make publicly available the precise location of the genome segment that is amplified in PCR tests and what antibodies are detected in serological tests. Many companies regard this information as commercially sensitive. Much attention has focused on the magnitude of R t at time t. But how precise is the measurement of R t and what confidence should be placed on the ranges of values (region by region in the UK) reported by SAGE? Many sources of variability exist (figure ). 13 There is uncertainty around some of the key epidemiological processes that determine the magnitude of R t. These include the fraction of infections that are asymptomatic, how infectious asymptomatic infections typically are, and the duration of the infectious period before symptoms appear. Also of importance is the probability distribution of the generation of secondary cases,17, 18, 19 which is overdispersed such that most infected individuals transmit none or a few infections, and a few individuals transmit many—the so-called super-spreading events. 20 Contact tracing data provide crucial insights on this distribution, which has important consequences for COVID-19 control. 21 Figure Simulations of the possible patterns of COVID-19 spread in the UK in 2020, taking account of parameter uncertainty The simulations of COVID-19 spread in the UK shown in this figure are illustrative, not predictive. One way of examining epidemiological uncertainty is to simulate the epidemic by sampling from the full range of parameter estimates in the current literature. As an illustration, we assume that all values of the parameters are equally likely and use Latin Hypercube methods to sample the parameter space. 14 The graph shows a deterministic simulation of the epidemic in the UK, recording the incidence of infection over time in a population of 60 million people, based on the model described in the appendix. The solid line is the average prediction and the shaded area covers the 95% credible interval of the 100 showing (inset R t and r t in the week before lockdown). Uncertainty in key epidemiological parameters therefore generates much variability in estimates of R t and to a lesser extent r t. If we fix the parameter uncertainty, but instead take into account the negative binomial distribution of R t, much variability in R t and r t is again generated across a series of model runs. 15 The message from both these examples suggests that the credible intervals around both parameters, R t and r t, are much wider than those reported at present. 16 These sources of variation must be combined with others that are also of great importance, such as spatial location and social factors. A schematic representation of uncertainty in determining the magnitude of R t and the course of the COVID-19 epidemic in the UK is shown in the figure with further information in the appendix. Estimates of R t often rely on a model framework fitted to data on cases, deaths, or serology using Bayesian methods. What is assumed within the model therefore influences the numbers derived. Uncertainty must therefore be factored into the advice given to policy makers. Relying on R t estimates is not ideal, and greater emphasis should be placed on how the rate of decay in incidence (negative values in r t) is changing and analysis of the second derivative (the rate of change of the rate of change), which suggests dangers ahead in terms of the start of a new exponential growth phase in case numbers and associated morbidity and mortality if it decreases rapidly. By the end of July, 2020, in the UK, daily reports of confirmed cases had stabilised at a fairly low level, but they are starting to exhibit the beginning of an increasing phase. 7 The concern at present is that the value of r t (and concomitantly that of R t) is expected to increase as physical distancing behaviours relax. All efforts must be made to increase the volume of testing, establish large-scale national serological studies, undertake more whole genome sequencing of the virus in isolates from people who test positive for infection to assess who infects whom, and to vigorously pursue enhancing trace, treat, and isolate activities with more reliance on, and support for, local authorities to gather data in the communities they understand. The level of herd immunity required to eliminate SARS-CoV-2 transmission, when and if a COVID-19 vaccine becomes available that gives a defined duration of protection, is determined by the magnitude of R 0 (the basic reproduction number). Part way through the epidemic in the UK, when only herd immunity created by past infection is acting, the magnitude of R t is the crucial determinant of what proportion of the population must be effectively immunised to halt transmission. Studies in the general population in the UK suggest the level of infection-induced herd immunity is low, with large variation in the percentage of the general population with antibodies to SARS-CoV-2, ranging from 0·5% to nearly 15% in different regions. 22 Progress on COVID-19 vaccine development has been encouraging and it might result in the availability of a vaccine earlier than expected in the UK, if phase 3 studies go well.23, 24 Then the challenges will include manufacturing a vaccine at scale and creating a high demand in the public such that more than 60% (if R 0 is around 2·5 in value) of the UK population are immunised. 25 Immunisation with a COVID-19 vaccine might have to be repeated annually if the duration of immunity is short, as suspected to be the case for other coronaviruses. 26 When providing estimates of the key epidemiological parameters about COVID-19 to inform policy, as noted by George Bernard Shaw, the single biggest problem in communicating uncertainty is the illusion that it has taken place. Linked to this problem is that of selective hearing, with individuals typically hearing what they want to hear within the wide uncertainty bounds, whether they are policy makers, the media, or the public. A priority for the new Joint Biosecurity Centre will be to advise caution over the coming months in relaxing physical distancing measures when uncertainty in the current and future course of the epidemic is so high.

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          Most cited references15

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          An mRNA Vaccine against SARS-CoV-2 — Preliminary Report

          Abstract Background The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) emerged in late 2019 and spread globally, prompting an international effort to accelerate development of a vaccine. The candidate vaccine mRNA-1273 encodes the stabilized prefusion SARS-CoV-2 spike protein. Methods We conducted a phase 1, dose-escalation, open-label trial including 45 healthy adults, 18 to 55 years of age, who received two vaccinations, 28 days apart, with mRNA-1273 in a dose of 25 μg, 100 μg, or 250 μg. There were 15 participants in each dose group. Results After the first vaccination, antibody responses were higher with higher dose (day 29 enzyme-linked immunosorbent assay anti–S-2P antibody geometric mean titer [GMT], 40,227 in the 25-μg group, 109,209 in the 100-μg group, and 213,526 in the 250-μg group). After the second vaccination, the titers increased (day 57 GMT, 299,751, 782,719, and 1,192,154, respectively). After the second vaccination, serum-neutralizing activity was detected by two methods in all participants evaluated, with values generally similar to those in the upper half of the distribution of a panel of control convalescent serum specimens. Solicited adverse events that occurred in more than half the participants included fatigue, chills, headache, myalgia, and pain at the injection site. Systemic adverse events were more common after the second vaccination, particularly with the highest dose, and three participants (21%) in the 250-μg dose group reported one or more severe adverse events. Conclusions The mRNA-1273 vaccine induced anti–SARS-CoV-2 immune responses in all participants, and no trial-limiting safety concerns were identified. These findings support further development of this vaccine. (Funded by the National Institute of Allergy and Infectious Diseases and others; mRNA-1273 ClinicalTrials.gov number, NCT04283461).
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            Safety and immunogenicity of the ChAdOx1 nCoV-19 vaccine against SARS-CoV-2: a preliminary report of a phase 1/2, single-blind, randomised controlled trial

            Summary Background The pandemic of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) might be curtailed by vaccination. We assessed the safety, reactogenicity, and immunogenicity of a viral vectored coronavirus vaccine that expresses the spike protein of SARS-CoV-2. Methods We did a phase 1/2, single-blind, randomised controlled trial in five trial sites in the UK of a chimpanzee adenovirus-vectored vaccine (ChAdOx1 nCoV-19) expressing the SARS-CoV-2 spike protein compared with a meningococcal conjugate vaccine (MenACWY) as control. Healthy adults aged 18–55 years with no history of laboratory confirmed SARS-CoV-2 infection or of COVID-19-like symptoms were randomly assigned (1:1) to receive ChAdOx1 nCoV-19 at a dose of 5 × 1010 viral particles or MenACWY as a single intramuscular injection. A protocol amendment in two of the five sites allowed prophylactic paracetamol to be administered before vaccination. Ten participants assigned to a non-randomised, unblinded ChAdOx1 nCoV-19 prime-boost group received a two-dose schedule, with the booster vaccine administered 28 days after the first dose. Humoral responses at baseline and following vaccination were assessed using a standardised total IgG ELISA against trimeric SARS-CoV-2 spike protein, a muliplexed immunoassay, three live SARS-CoV-2 neutralisation assays (a 50% plaque reduction neutralisation assay [PRNT50]; a microneutralisation assay [MNA50, MNA80, and MNA90]; and Marburg VN), and a pseudovirus neutralisation assay. Cellular responses were assessed using an ex-vivo interferon-γ enzyme-linked immunospot assay. The co-primary outcomes are to assess efficacy, as measured by cases of symptomatic virologically confirmed COVID-19, and safety, as measured by the occurrence of serious adverse events. Analyses were done by group allocation in participants who received the vaccine. Safety was assessed over 28 days after vaccination. Here, we report the preliminary findings on safety, reactogenicity, and cellular and humoral immune responses. The study is ongoing, and was registered at ISRCTN, 15281137, and ClinicalTrials.gov, NCT04324606. Findings Between April 23 and May 21, 2020, 1077 participants were enrolled and assigned to receive either ChAdOx1 nCoV-19 (n=543) or MenACWY (n=534), ten of whom were enrolled in the non-randomised ChAdOx1 nCoV-19 prime-boost group. Local and systemic reactions were more common in the ChAdOx1 nCoV-19 group and many were reduced by use of prophylactic paracetamol, including pain, feeling feverish, chills, muscle ache, headache, and malaise (all p<0·05). There were no serious adverse events related to ChAdOx1 nCoV-19. In the ChAdOx1 nCoV-19 group, spike-specific T-cell responses peaked on day 14 (median 856 spot-forming cells per million peripheral blood mononuclear cells, IQR 493–1802; n=43). Anti-spike IgG responses rose by day 28 (median 157 ELISA units [EU], 96–317; n=127), and were boosted following a second dose (639 EU, 360–792; n=10). Neutralising antibody responses against SARS-CoV-2 were detected in 32 (91%) of 35 participants after a single dose when measured in MNA80 and in 35 (100%) participants when measured in PRNT50. After a booster dose, all participants had neutralising activity (nine of nine in MNA80 at day 42 and ten of ten in Marburg VN on day 56). Neutralising antibody responses correlated strongly with antibody levels measured by ELISA (R 2=0·67 by Marburg VN; p<0·001). Interpretation ChAdOx1 nCoV-19 showed an acceptable safety profile, and homologous boosting increased antibody responses. These results, together with the induction of both humoral and cellular immune responses, support large-scale evaluation of this candidate vaccine in an ongoing phase 3 programme. Funding UK Research and Innovation, Coalition for Epidemic Preparedness Innovations, National Institute for Health Research (NIHR), NIHR Oxford Biomedical Research Centre, Thames Valley and South Midland's NIHR Clinical Research Network, and the German Center for Infection Research (DZIF), Partner site Gießen-Marburg-Langen.
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              Potent neutralizing antibodies against SARS-CoV-2 identified by high-throughput single-cell sequencing of convalescent patients’ B cells

              Summary The COVID-19 pandemic urgently needs therapeutic and prophylactic interventions. Here we report the rapid identification of SARS-CoV-2 neutralizing antibodies by high-throughput single-cell RNA and VDJ sequencing of antigen-enriched B cells from 60 convalescent patients. From 8,558 antigen-binding IgG1+ clonotypes, 14 potent neutralizing antibodies were identified with the most potent one, BD-368-2, exhibiting an IC50 of 1.2 ng/mL and 15 ng/mL against pseudotyped and authentic SARS-CoV-2, respectively. BD-368-2 also displayed strong therapeutic and prophylactic efficacy in SARS-CoV-2-infected hACE2-transgenic mice. Additionally, the 3.8Å Cryo-EM structure of a neutralizing antibody in complex with the spike-ectodomain trimer revealed the antibody’s epitope overlaps with the ACE2 binding site. Moreover, we demonstrated that SARS-CoV-2 neutralizing antibodies could be directly selected based on similarities of their predicted CDR3H structures to those of SARS-CoV neutralizing antibodies. Altogether, we showed that human neutralizing antibodies could be efficiently discovered by high-throughput single B-cell sequencing in response to pandemic infectious diseases.
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                Author and article information

                Contributors
                Journal
                Lancet
                Lancet
                Lancet (London, England)
                Elsevier Ltd.
                0140-6736
                1474-547X
                3 August 2020
                3 August 2020
                Affiliations
                [a ]Medical Research Council Centre for Global Infectious Disease Analysis, Department of Infectious Disease Epidemiology, School of Public Health, Imperial College London, London W2 1PG, UK
                [b ]Big Data Institute, Li Ka Shing Centre for Health Information and Discovery, University of Oxford, Oxford, UK
                [c ]Department of Respiratory Sciences, University of Leicester, Leicester, UK
                Article
                S0140-6736(20)31689-5
                10.1016/S0140-6736(20)31689-5
                7398685
                db263ef1-bdb9-4842-a88f-9e8991cc762f
                © 2020 Elsevier Ltd. All rights reserved.

                Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.

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