Master Question List for COVID-19 (Caused by SARS-Cov-2) Weekly Report 13 October 2020
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Immunogenicity of Clinically Relevant SARS-Cov-2 Vaccines
Preprints (www.preprints.org) | NOT PEER-REVIEWED | Posted: 7 September 2020 1 Immunogenicity of clinically relevant SARS-CoV-2 vaccines in non-human primates and humans P. J. Klasse (1,*), Douglas F. Nixon (2,*) and John P. Moore (1,+) 1 Department of Microbiology and Immunology; 2 Division of Infectious Diseases, Department of Medicine, Weill Cornell Medical College, New York, NY 10065 *These authors contributed equally +Correspondence: [email protected] Short title: SARS-CoV-2 vaccine immunogenicity Key words: SARS-CoV-2, S-protein, RBD, COVID-19, neutralizing antibodies, serology, T- cells, vaccines, animal models, Operation Warp Speed © 2020 by the author(s). Distributed under a Creative Commons CC BY license. Preprints (www.preprints.org) | NOT PEER-REVIEWED | Posted: 7 September 2020 2 Abstract Multiple preventive vaccines are being developed to counter the COVID-19 pandemic. The leading candidates have now been evaluated in non-human primates (NHPs) and human Phase 1 and/or Phase 2 clinical trials. Several vaccines have already advanced into Phase 3 efficacy trials, while others will do so before the end of 2020. Here, we summarize what is known of the antibody and T-cell immunogenicity of these vaccines in NHPs and humans. To the extent possible, we compare how the vaccines have performed, taking into account the use of different assays to assess immunogenicity and inconsistencies in how the resulting data are presented. We also summarize the outcome of SARS-CoV-2 challenge experiments in immunized macaques, while noting variations in the protocols used, including but not limited to the virus challenge doses. Preprints (www.preprints.org) | NOT PEER-REVIEWED | Posted: 7 September 2020 3 Introduction The COVID-19 pandemic rages unabated and may continue to do so until there is a safe, effective and widely used protective vaccine. -
(MGH) COVID-19 Treatment Guidance
Version 8.0 4/28/2021 10:00AM © Copyright 2020 The General Hospital Corporation. All Rights Reserved. Massachusetts General Hospital (MGH) COVID-19 Treatment Guidance This document was prepared (in March, 2020-April, 2021) by and for MGH medical professionals (a.k.a. clinicians, care givers) and is being made available publicly for informational purposes only, in the context of a public health emergency related to COVID-19 (a.k.a. the coronavirus) and in connection with the state of emergency declared by the Governor of the Commonwealth of Massachusetts and the President of the United States. It is neither an attempt to substitute for the practice of medicine nor as a substitute for the provision of any medical professional services. Furthermore, the content is not meant to be complete, exhaustive, or a substitute for medical professional advice, diagnosis, or treatment. The information herein should be adapted to each specific patient based on the treating medical professional’s independent professional judgment and consideration of the patient’s needs, the resources available at the location from where the medical professional services are being provided (e.g., healthcare institution, ambulatory clinic, physician’s office, etc.), and any other unique circumstances. This information should not be used to replace, substitute for, or overrule a qualified medical professional’s judgment. This website may contain third party materials and/or links to third party materials and third party websites for your information and convenience. Partners is not responsible for the availability, accuracy, or content of any of those third party materials or websites nor does it endorse them. -
Using Cross-Species Vaccination Approaches to Counter Emerging
PERSPECTIVES adjuvant combinations to inform ‘go’ or ‘no- go’ decisions with regard to subsequent Using cross- species vaccination development of promising vaccine candidates (Fig. 1). approaches to counter emerging Most human infectious diseases have an animal origin, with more than 70% of infectious diseases emerging infectious diseases that affect humans initially crossing over from 8 George M. Warimwe , Michael J. Francis , Thomas A. Bowden, animals . Generating wider knowledge of how pathogens behave in animals can Samuel M. Thumbi and Bryan Charleston give indications of how to develop control Abstract | Since the initial use of vaccination in the eighteenth century, our strategies for human diseases, and vice understanding of human and animal immunology has greatly advanced and a wide versa. ‘One Health vaccinology’, a concept in which synergies in human and veterinary range of vaccine technologies and delivery systems have been developed. The immunology are identified and exploited COVID-19 pandemic response leveraged these innovations to enable rapid for vaccine development, could transform development of candidate vaccines within weeks of the viral genetic sequence our ability to control such emerging being made available. The development of vaccines to tackle emerging infectious infectious diseases. Due to similarities in diseases is a priority for the World Health Organization and other global entities. host–pathogen interactions, the natural More than 70% of emerging infectious diseases are acquired from animals, with animal hosts of a zoonotic infection may be the most appropriate model to study the some causing illness and death in both humans and the respective animal host. Yet disease and evaluate vaccine performance9. -
A Comparative History of Oil and Gas Markets and Prices: Is 2020 Just an Extreme Cyclical Event Or an Acceleration of the Energy Transition?
April 2020 A Comparative History of Oil and Gas Markets and Prices: is 2020 just an extreme cyclical event or an acceleration of the energy transition? Introduction Natural gas markets have gone through an unprecedented transformation. Demand growth for this relatively clean, plentiful, versatile and now relatively cheap fuel has been increasing faster than for other fossil fuels.1 Historically a `poor relation’ of oil, gas is now taking centre stage. New markets, pricing mechanisms and benchmarks are being developed, and it is only natural to be curious about the direction these developments are taking. The oil industry has had a particularly rich and well recorded history, making it potentially useful for comparison. However, oil and gas are very different fuels and compete in different markets. Their paths of evolution will very much depend on what happens in the markets for energy sources with which they compete. Their history is rich with dominant companies, government intervention and cycles of boom and bust. A common denominator of virtually all energy industries is a tendency towards natural monopoly because they have characteristics that make such monopolies common. 2 Energy projects tend to require multibillion – often tens of billions of - investments with long gestation periods, with assets that can only be used for very specific purposes and usually, for very long-time periods. Natural monopolies are generally resolved either by new entrants breaking their integrated market structures or by government regulation. Historically, both have occurred in oil and gas markets.3 As we shall show, new entrants into the oil market in the 1960s led to increased supply at lower prices, and higher royalties, resulting in the collapse of control by the major oil companies. -
Immunogenicity of a New Gorilla Adenovirus Vaccine Candidate for COVID-19
bioRxiv preprint doi: https://doi.org/10.1101/2020.10.22.349951; this version posted October 22, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. Immunogenicity of a new gorilla adenovirus vaccine candidate for COVID-19 Stefania Capone1,6, Angelo Raggioli1,6, Michela Gentile1, Simone Battella1, Armin Lahm1, Andrea Sommella1, Alessandra Maria Contino1, Richard A. Urbanowicz2,3,4, Romina Scala1, Federica Barra1, Adriano Leuzzi1, Eleonora Lilli1, Giuseppina Miselli1, Alessia Noto1, Maria Ferraiuolo1, Francesco Talotta1, Theocharis Tsoleridis2,3,4, Concetta Castilletti5, Giulia Matusali5, Francesca Colavita5, Daniele Lapa5, Silvia Meschi5, Maria Capobianchi5, Marco Soriani1, Antonella Folgori1, Jonathan K. Ball2,3,4, Stefano Colloca1 and Alessandra Vitelli1* 1 ReiThera Srl, Rome, Italy 2 School of Life Sciences, The University of Nottingham, UK 3 NIHR Nottingham Biomedical Research Centre, The University of Nottingham, UK 4 Wolfson Centre for Emerging Virus Research, The University of Nottingham, UK 5 National Institute for Infectious Diseases "Lazzaro Spallanzani" IRCCS 6 These authors contributed equally * [email protected] ABSTRACT The COVID-19 pandemic caused by the emergent SARS-CoV-2 coronavirus threatens global public health and there is an urgent need to develop safe and effective vaccines. Here we report the generation and the preclinical evaluation of a novel replication-defective gorilla adenovirus-vectored vaccine encoding the pre-fusion stabilized Spike (S) protein of SARS-CoV2. We show that our vaccine candidate, GRAd- COV2, is highly immunogenic both in mice and macaques, eliciting both functional antibodies which neutralize SARS-CoV-2 infection and block Spike protein binding to the ACE2 receptor, and a robust, Th1- dominated cellular response in the periphery and in the lung. -
Progress in the Development of Potential Therapeutics and Vaccines Against COVID-19 Pandemic
Acta Scientific Pharmaceutical Sciences (ISSN: 2581-5423) Volume 5 Issue 7 July 2021 Review Article Progress in the Development of Potential Therapeutics and Vaccines against COVID-19 Pandemic Abhishek Kumar Yadav, Shubham Kumar and Vikramdeep Monga* Received: May 02, 2021 Department of Pharmaceutical Chemistry, ISF College of Pharmacy, Moga, Punjab, Published: June 09, 2021 India © All rights are reserved by Vikramdeep *Corresponding Author: Vikramdeep Monga, Department of Pharmaceutical Monga., et al. Chemistry, ISF College of Pharmacy, Moga, Punjab, India. Abstract Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes COVID-19 or coronavirus disease 2019 and the same has been declared as a global pandemic by WHO which marked the third introduction of a virulent coronavirus into human society. This a threat to human life worldwide. Considerable efforts have been made for developing effective and safe drugs and vaccines against is a highly pathogenic human coronavirus in which pneumonia of unknown origin was identified in China in December 2019 and is SARS-CoV-2. The current situation and progress in the development of various therapeutic candidates including vaccines in preclini- cal and clinical studies have been described in the manuscript. Until now, many people have been infected with this lethal virus, and a lot of people have died from this COVID-19. This viral disease spreads by coming in contact with an infected person. Understand- ing of SARS-CoV-2 is growing in relation to its epidemiology, virology, and clinical management strategies. Till date, very few drugs or vaccines have been developed or approved for the treatment of this deadly disease of COVID-19 and many candidates are under the clinical development pipeline. -
Impact of SARS-Cov-2 Variant on the Severity of Maternal Infection and Perinatal Outcomes: Data from the UK Obstetric Surveillan
medRxiv preprint doi: https://doi.org/10.1101/2021.07.22.21261000; this version posted July 25, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY 4.0 International license . Impact of SARS-CoV-2 variant on the severity of maternal infection and perinatal outcomes: Data from the UK Obstetric Surveillance System national cohort. Nicola Vousden PhD1, Rema Ramakrishnan PhD1, Kathryn Bunch MA1, Edward Morris MD2, Nigel Simpson MBBS3, Christopher Gale PhD4, Patrick O’Brien MBBCh,2,5, Maria Quigley MSc1, Peter Brocklehurst MSc6, Jennifer J Kurinczuk MD1, Marian Knight DPhil1 1National Perinatal Epidemiology Unit, Nuffield Department of Population Health, University of Oxford, UK 2Royal College of Obstetricians and Gynaecologists, London, UK 3Department of Women's and Children's Health, School of Medicine, University of Leeds, UK 4Neonatal Medicine, School of Public Health, Faculty of Medicine, Imperial College London, London, UK 5Institute for Women’s Health, University College London, London, UK 6Birmingham Clinical Trials Unit, Institute of Applied Health Research, University of Birmingham, UK *Corresponding author: Marian Knight National Perinatal Epidemiology Unit, Nuffield Department of Population Health, University of Oxford, UK 01865 289700 [email protected] NOTE: This preprint reports new research that has not been certified by peer review and should not be used to guide clinical practice. 1 medRxiv preprint doi: https://doi.org/10.1101/2021.07.22.21261000; this version posted July 25, 2021. -
COVID-19 Vaccine Candidates in Development, Special Focus on Mrna and Viral Vector Platforms Dr
To view an archived recording of this presentation please click the following link: http://pho.adobeconnect.com/pbwjspa1fh9a/ Please scroll down this file to view a copy of the slides from the session. Helpful tips when viewing the recording: • The default presentation format includes showing the “event index”. To close the events index, please click on the following icon and hit “close” • If you prefer to view the presentation in full screen mode, please click on the following icon in the top right hand corner of the share screen PublicHealthOntario.ca 2 COVID-19 Vaccine Candidates in Development, special focus on mRNA and viral vector platforms Dr. Marina Salvadori and Dr. April Killikelly Centre for Immunization and Respiratory Infectious Diseases, PHAC October 1, 2020 Disclosures • None of the presenters at this session have received financial support or in-kind support from a commercial sponsor. • None of the presenters have potential conflicts of interest to declare. 2 OBJECTIVE • Describe the mechanism of action of mRNA, viral vector and protein- based vaccines • Discuss the evidence available for vaccines in development that may be available in Canada if proved safe and effective 3 Global COVID-19 Vaccine Development Landscape: • As of September 24, 2020, 63 clinical trials have been registered for developmental vaccine candidates against COVID-19. • Two anti-SARS-COV-2 vaccine candidates have obtained regulatory authorization to initiate clinical trials in Canada and one vaccine candidate has begun clinical testing in Canada (Medicago). 4 Lead Candidate COVID-19 Vaccine Development Landscape: Protein-based (top box), viral vector based (middle box) and mRNA (bottom box) and technology constitute the majority of the front running COVID-19 vaccine technologies. -
Everything You Needed to Know About LNG … but Were Afraid to Ask
Everything you needed to know about LNG … but were afraid to ask. – Part I James Ashworth Lead Consultant TRI-ZEN International Pte Ltd, Singapore Glasgow Technology and Innovation Centre (TIC). , 14-17 September 2015 Glasgow 2015 2 Glasgow – Global Capital of Irreverence www.tri-zen.com 3 Thailand LAND OF SMILES AND OPPORTUNITIES 4 Thailand A land where everybody is an expert in Stress Mechanics 5 Thailand A land where you can be run over by a shop. 6 Thailand A world leader in space technology LNG Bunkering Mediterranean Summit 8 Workshop Early Gas Carriers ss “Methane Princess” ss “Geomitra” Brunei, Lumut LNG Liquefaction Plant loading arm LNG Fuelled Shipping Outlook Glasgow 2015 11 Headlines LNG will become the dominant marine fuel globally by 2030 This will double LNG demand from ~300m mt to ~600m mt Only 20% of shipping can be converted to LNG 80% of shipping (1 bn dwt) needs to be scrapped and replaced Market drivers will prevail This will fill global shipyard capacity, create jobs and stimulate economic development Exhaust Gas Treatment solutions make sense in some cases, but are not a sustainable solution The global LNG Supply Chain needs to diversify Globally The USA is set to become the world’s biggest energy exporter by 2020 Saudi Arabia is set to become a net energy importer by 2030 Glasgow 2015 12 Global Outlook Global Outlook Economic Oil Market Gas Market Gas as LNG Current Issues www.tri-zen.com 13 Global Outlook Economic Outlook Uneven global recovery continues, and the growth forecast for the world economy has slowed to 3.3% for 2014. -
Adenoviral Vector COVID-19 Vaccines: Process and Cost Analysis
processes Article Adenoviral Vector COVID-19 Vaccines: Process and Cost Analysis Rafael G. Ferreira 1,* , Neal F. Gordon 2, Rick Stock 2 and Demetri Petrides 3 1 Intelligen Brasil, Sao Paulo 01227-200, Brazil 2 BDO USA, LLP, Boston, MA 02110, USA; [email protected] (N.F.G.); [email protected] (R.S.) 3 Intelligen, Inc., Scotch Plains, NJ 07076, USA; [email protected] * Correspondence: [email protected] Abstract: The COVID-19 pandemic has motivated the rapid development of numerous vaccines that have proven effective against SARS-CoV-2. Several of these successful vaccines are based on the adenoviral vector platform. The mass manufacturing of these vaccines poses great challenges, especially in the context of a pandemic where extremely large quantities must be produced quickly at an affordable cost. In this work, two baseline processes for the production of a COVID-19 adenoviral vector vaccine, B1 and P1, were designed, simulated and economically evaluated with the aid of the software SuperPro Designer. B1 used a batch cell culture viral production step, with a viral titer of 5 × 1010 viral particles (VP)/mL in both stainless-steel and disposable equipment. P1 used a perfusion cell culture viral production step, with a viral titer of 1 × 1012 VP/mL in exclusively disposable equipment. Both processes were sized to produce 400 M/yr vaccine doses. P1 led to a smaller cost per dose than B1 ($0.15 vs. $0.23) and required a much smaller capital investment ($126 M vs. $299 M). The media and facility-dependent expenses were found to be the main contributors to the operating cost. -
An Examination of COVID-19 Medications' Effectiveness
healthcare Review An Examination of COVID-19 Medications’ Effectiveness in Managing and Treating COVID-19 Patients: A Comparative Review Mahmoud Al-Masaeed 1,* , Mohammad Alghawanmeh 2, Ashraf Al-Singlawi 3 , Rawan Alsababha 4 and Muhammad Alqudah 1 1 Faculty of Health and Medicine, University of Newcastle, Callaghan 2308, Australia; [email protected] 2 Faculty of Pharmacy, Philadelphia University, Amman 19392, Jordan; [email protected] 3 Independent Scholar, Amman 11731, Jordan; [email protected] 4 School of nursing and Midwifery, Western Sydney University, Sydney 2560, Australia; [email protected] * Correspondence: [email protected] Abstract: Background: The review seeks to shed light on the administered and recommended COVID- 19 treatment medications through an evaluation of their efficacy. Methods: Data were collected from key databases, including Scopus, Medline, Google Scholar, and CINAHL. Other platforms included WHO and FDA publications. The review’s literature search was guided by the WHO Citation: Al-Masaeed, M.; solidarity clinical trials for COVID-19 scope and trial-assessment parameters. Results: The findings Alghawanmeh, M.; Al-Singlawi, A.; indicate that the use of antiretroviral drugs as an early treatment for COVID-19 patients has been Alsababha, R.; Alqudah, M. An useful. It has reduced hospital time, hastened the clinical cure period, delayed and reduced the Examination of COVID-19 need for mechanical and invasive ventilation, and reduced mortality rates. The use of vitamins, Medications’ Effectiveness in minerals, and supplements has been linked to increased immunity and thus offering the body a Managing and Treating COVID-19 fighting chance. Nevertheless, antibiotics do not correlate with improving patients’ wellbeing and Patients: A Comparative Review. -
Protective Zika Vaccines Engineered to Eliminate Enhancement of Dengue Infection Via Immunodominance Switch
ARTICLES https://doi.org/10.1038/s41590-021-00966-6 Protective Zika vaccines engineered to eliminate enhancement of dengue infection via immunodominance switch Lianpan Dai 1,2,3,8 ✉ , Kun Xu3,8, Jinhe Li2,4,8, Qingrui Huang5, Jian Song 1, Yuxuan Han2, Tianyi Zheng2,4, Ping Gao2,4, Xuancheng Lu6, Huabing Yang 5, Kefang Liu7, Qianfeng Xia3, Qihui Wang 1, Yan Chai1, Jianxun Qi 1, Jinghua Yan 5 ✉ and George F. Gao 1,2,4 ✉ Antibody-dependent enhancement (ADE) is an important safety concern for vaccine development against dengue virus (DENV) and its antigenically related Zika virus (ZIKV) because vaccine may prime deleterious antibodies to enhance natural infections. Cross-reactive antibodies targeting the conserved fusion loop epitope (FLE) are known as the main sources of ADE. We design ZIKV immunogens engineered to change the FLE conformation but preserve neutralizing epitopes. Single vaccination conferred sterilizing immunity against ZIKV without ADE of DENV-serotype 1–4 infections and abrogated maternal–neonatal transmis- sion in mice. Unlike the wild-type-based vaccine inducing predominately cross-reactive ADE-prone antibodies, B cell profiling revealed that the engineered vaccines switched immunodominance to dispersed patterns without DENV enhancement. The crystal structure of the engineered immunogen showed the dimeric conformation of the envelope protein with FLE disruption. We provide vaccine candidates that will prevent both ZIKV infection and infection-/vaccination-induced DENV ADE. IKV is a mosquito-borne pathogen belonging to the genus models12,13,19,20. More importantly, a recent study of pediatric cohorts Flavivirus in the family Flaviviridae1. The 2015–2016 ZIKV in Nicaragua clearly shows that previous ZIKV infection enhanced epidemic spread to 84 countries worldwide, including future risk of DENV2 disease and severity, as well as DENV3 sever- Z2,3 21,22 China .