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Saturday, April 24, 2021

Pandemic oxygen demand lifts Air Liquide's Q1 sales

 

French industrial gas company Air Liquide posted higher-than-expected first-quarter sales on Friday, driven by strong demand for medical oxygen during the coronavirus pandemic and a strong rebound in China.

The company, which supplies gases such as oxygen, nitrogen and hydrogen to factories and hospitals, saw gas and services sales in China jump nearly 13% on a comparable basis from the year earlier period, driven by industrial demand.

Healthcare revenues rose 10%, boosted by exceptionally high sales of medical oxygen, essential for critically ill COVID-19 patients.

In a call with analysts, Executive Vice President Francois Jackow said the group had quadrupled the amount of medical oxygen it was supplying to India, where cases are exceeding 330,000 a day and overwhelming the country's health system.

"To give an order of magnitude for the whole country, there is probably close to 800 tonnes per day of medical oxygen demand," he said. "What we see today and for the past few weeks is an increase by ten-fold."

Jackow said Air Liquide had switched nearly all its liquid oxygen production to healthcare in the country.

Several Indian hospitals said they had almost exhausted their oxygen supplies on Thursday, as a dire shortage caused states to closely guard their supplies and even post armed police at production plants.

Demand for medical gas also increased in Latin America, notably in Brazil, where Jackow reported "unfortunately, very, very high growth".

Air Liquide expects to secure antitrust approval for its purchase of the world's biggest oxygen production site in Secunda, South Africa, from chemicals firm Sasol by the end of June.

The group confirmed its 2021 growth targets, on the back of a 3.8% rise in comparable first-quarter sales to 5.33 billion euros ($6.41 billion), topping analysts' 5.25 billion forecast.

https://www.marketscreener.com/news/latest/Pandemic-oxygen-demand-lifts-Air-Liquide-s-Q1-sales--33043869/

Friday, April 23, 2021

New malaria vaccine proves highly effective; COVID shows how quickly could be deployed

 Coronavirus vaccines have been developed and deployed in record time, but as global rollout has progressed, too few doses have been made available in low-income countries. It's a stark reminder that when it comes to infectious diseases, the world's poorest often get left behind.

This is a problem that extends far beyond COVID-19. In Africa, for example, malaria has probably caused four times as many deaths as COVID-19 over the past year. Thankfully, our new research shows that an effective  against  could now be closer than ever before.

For the first time, a vaccine has shown high efficacy in trials—preventing the disease 77% of the time among those receiving it. This is a landmark achievement. The WHO's target efficacy for malaria vaccines is over 75%. Until now, this level has never been reached.

The speed and success of developing COVID-19 vaccines shows what's possible, and should be an inspiration to get this  finished, licensed and distributed. It's important not just because of the threat malaria poses, but also because investing in vaccines can help prepare us for the next pandemic. Work on this vaccine helped speed the development of the Oxford vaccine for COVID-19 as well.

The World Health Organization estimates there were 229 million cases of malaria in 2019. Globally, malaria's annual death toll stands at over 400,000, with no improvement in the last five years. Two-thirds of this terrible loss is among African children under five years of age.

Billions of dollars are being spent each year on bed nets, insecticide spraying and antimalarial drugs just to keep death rate as it is. New technologies are needed, especially as the WHO is targeting a 90% reduction in deaths by 2030.

No malaria vaccine has yet been authorised for use, though the idea of controlling malaria by vaccination has been around for a long time. The first scientific report was from Algiers in 1910. Clinical trials began in the 1940s, got serious from the 1980s onwards and, today, over 140 malaria vaccine candidates have been tested in humans.

But none has progressed to approval and deployment. The science is tough. The  is complex, with more than 5,000 genes, meaning it has many different characteristics for vaccine designers to choose to target. SARS-CoV-2, the virus that causes COVID-19, has just 12 genes, and its spike protein was the obvious target for vaccine scientists.

Malaria parasites have evolved with humans and their ancestors over the last 30 million years, not only generating a multitude of strains but also impacting our own evolution, with gene variants that lessened the effects of malaria being passed on over time. Worse still, these parasites generate chronic infections in millions, suppressing the human immune response that a vaccine tries to generate.

New success with a new vaccine

But progress on malaria vaccine development is accelerating, as illustrated by a new report from a multi-national group of researchers, including myself, published in The Lancet. The team of Professor Halidou Tinto, based in Ouagadougou, Burkina Faso, studied the new R21 malaria vaccine in 450 children—the key population where a vaccine is most urgently needed. They found it to be safe and have unprecedented efficacy in those aged 5-17 months.

In this controlled trial, 105 of the 147 children who received a placebo contracted malaria. But of the 292 who received a dose of the vaccine, only 81 contracted the disease—surpassing the WHO's 75% target for protection. A phase 3 trial—to test the safety and efficacy of the vaccine in a much larger number of people—will start in four African countries in late April 2021, aiming for accelerated approvals if successful.

Scientists in four continents contributed to the design and testing of this promising vaccine. Design and early development took place at the Jenner Institute at the University of Oxford, where malaria vaccine  have been pursued since 1999. "Challenge" studies in Oxford, Southampton and London, where volunteers are deliberately infected with malaria by mosquito bites to test vaccine efficacy, highlighted the potential of the R21 vaccine. An adjuvant component for the vaccine is required and provided by Novavax, a biotechnology company in the US and Sweden.

Manufacturing of the vaccine is ongoing at the world's largest vaccine supplier, the Serum Institute of India. This malaria partnership with was already in place last year when COVID-19 struck, allowing us to pivot rapidly to manufacturing the Oxford  vaccine. (The method it uses for delivery, a chimpanzee adenovirus called ChAdOx1, is a technology previously tested for use against malaria.) Having this collaboration already in place, even prior to our partnership with AstraZeneca, helped the Indian company accelerate its COVID-19 vaccine manufacturing such that today it is producing more doses than anywhere else.

Could the same rapid, large-scale production happen for malaria vaccines? Maybe, but there are risks. Another promising vaccine candidate—from GlaxoSmithKline, called RTS,S—hit safety issues in its major phase 3 trial five years ago, and this has delayed its approval while further large-scale assessments take place.

Financing will also be required for malaria vaccine deployment, but with the low-cost large-scale manufacturing capacity in India available, an inexpensive widely accessible vaccine should be achievable. However, as COVID-19 is increasing in several parts of Africa, this could potentially impact the R21 vaccine phase 3 trials that are starting soon in Mali, Burkina Faso, Tanzania and Kenya.

The UK has long been a force in global health research, and fighting malaria is a flagship activity. Funding has been hit hard by this year's reduction in the overseas aid budget. But COVID-19 has highlighted the importance of maintaining capacity in vaccine research and development, as well as the feasibility of moving more quickly than ever before to vaccine approval and supply.

One lasting benefit of a terrible pandemic might be a quicker route to a malaria vaccine and a safer future for children in some of the world's poorest countries.

https://medicalxpress.com/news/2021-04-malaria-vaccine-highly-effective-covid.html

AstraZeneca vaccine benefits increase with age: EMA

 The EU's drug watchdog said Friday that a review of AstraZeneca's COVID-19 vaccine found its benefits increase with age and still outweigh the risks for adults despite links to blood clots.

The European Medicines Agency (EMA) was presenting its findings after the European Commission asked it to look into concerns that prompted several countries to restrict its use to older people.

"It showed that the benefits of vaccination increase with increasing age and infection rates," the Amsterdam-based EMA said in statement.

"The benefits of Vaxzevria outweigh its risks in adults of all age groups; however, very rare cases of blood clots with low blood platelets have occurred following vaccination," it added, using the 's brand name.

The rare clots happened in around one in 100,000 people who received the vaccine, it said.

"Vaxzevria is effective at preventing hospitalisations, intensive care unit (ICU) admissions and deaths due to COVID-19. The most common side effects are usually mild or moderate and get better within a few days."

Despite reports that  cases were more prevalent among women, the EMA said that "there were insufficient data available from across the EU to provide further context on benefits and risks with regard to sex."

Blow to confidence

Public confidence in the AstraZeneca jab has taken a blow since the EMA said on April 7 that a very rare, but often fatal, form of blood clot affecting the brain should be listed as a side effect.

Clots are also being listed as a side effect of the J&J vaccine, which uses the same adenovirus vector technology as AstraZeneca, the EMA said earlier this week.

Brussels asked the EMA earlier this month to carry out further investigations, and the watchdog said its announcement on Friday was to "provide an update on the analysis of data" on AstraZeneca.

The EMA said it was also sharing the latest opinion issued by its human medicines committee "aimed at supporting national decision-making on how to best use the vaccine in their territories."

The regulator said on Tuesday that there had been 287 cases of the rare clots worldwide linked to AstraZeneca, 25 to the Pfizer-BioNTech vaccine, eight to the Johnson & Johnson shot and five to the Moderna jab.

The EU is now increasingly relying for its rollout on the BioNTech/Pfizer vaccine, which uses rival mRNA tech.

The European Commission is also looking to launch  against AstraZeneca for underdelivering COVID-19 vaccine doses to the EU, which hobbled its early rollout.

https://medicalxpress.com/news/2021-04-astrazeneca-vaccine-benefits-age-ema.html

UK launches COVID-19 Antivirals Taskforce to roll out innovative home treatments this fall

 

  • New Antivirals Taskforce could identify and deploy innovative COVID-19 treatments as early as autumn
  • Treatments could be taken at home after a positive test or exposure to COVID-19 to reduce transmission and speed up recovery
  • Drugs could help combat a rise in infections or new variants over the winter flu season

A new Antivirals Taskforce has been launched by the government to identify treatments for UK patients who have been exposed to COVID-19 to stop the infection spreading and speed up recovery time.

The taskforce will search for the most promising novel antiviral medicines that can be taken at home and support their development through clinical trials to ensure they can be rapidly rolled out to patients as early as the autumn.

The taskforce will also look at opportunities to onshore the manufacture of antiviral treatments.

The aim is to have at least 2 effective treatments this year, either in a tablet or capsule form, that the public can take at home following a positive COVID-19 test or exposure to someone with the virus.

This will be another vital tool to combat any future increase in infections and limit the impact of new variants, especially over the flu season later this year.

https://www.gov.uk/government/news/government-launches-covid-19-antivirals-taskforce-to-roll-out-innovative-home-treatments-this-autumn

Clinical Trends Among U.S. Adults Hospitalized with COVID-19, March-December 2020

 Shikha Garg, MD, MPH, Kadam Patel, MPH, Huong Pham, MPH, Pam Daily Kirley, MPH, Breanna Kawasaki, MPH, Kimberly Yousey-Hindes, MPH, Evan J. Anderson, MD, Andrew Weigel, MSW, Patricia A. Ryan, MS, Libby Reeg, MPH, Kathryn Como-Sabetti, MPH, Sarah Shrum Davis, MPH, Alison Muse, MPH, Nancy M. Bennett, MD, MS, Laurie Billing, MPH, Melissa Sutton, MD, MPH, H. Keipp Talbot, MD, Mary Hill, MPH, Jonathan Wortham, MD, Lindsay Kim, MD, Fiona Havers, MD, MHS, COVID-NET Surveillance Team

SARS-CoV-2 can recruit a haem metabolite to evade antibody immunity

 Annachiara Rosa1, 

  1. Valerie E. Pye1
  2. Carl Graham2
  3. Luke Muir3
  4. Jeffrey Seow2
  5. Kevin W. Ng4
  6. Nicola J. Cook1
DOI: DOI: 10.1126/sciadv.abg7607

PDF: https://advances.sciencemag.org/content/early/2021/04/22/sciadv.abg7607/tab-pdf

Abstract

The coronaviral spike is the dominant viral antigen and the target of neutralizing antibodies. We show that SARS-CoV-2 spike binds biliverdin and bilirubin, the tetrapyrrole products of haem metabolism, with nanomolar affinity. Using cryo-electron microscopy and X-ray crystallography, we mapped the tetrapyrrole interaction pocket to a deep cleft on the spike N-terminal domain (NTD). At physiological concentrations, biliverdin significantly dampened the reactivity of SARS-CoV-2 spike with immune sera and inhibited a subset of neutralizing antibodies. Access to the tetrapyrrole-sensitive epitope is gated by a flexible loop on the distal face of the NTD. Accompanied by profound conformational changes in the NTD, antibody binding requires relocation of the gating loop, which folds into the cleft vacated by the metabolite. Our results indicate that SARS-CoV-2 spike NTD harbors a dominant epitope, access to which can be controlled by an allosteric mechanism that is regulated through the recruitment of a metabolite.


https://advances.sciencemag.org/content/early/2021/04/22/sciadv.abg7607

SARS-CoV-2 Spike Protein Elicits Cell Signaling in Human Host Cells: Implications for Possible Consequences of COVID-19 Vaccines

 

 2  


PDF: https://www.mdpi.com/2076-393X/9/1/36/pdf

Abstract

The world is suffering from the coronavirus disease 2019 (COVID-19) pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). SARS-CoV-2 uses its spike protein to enter the host cells. Vaccines that introduce the spike protein into our body to elicit virus-neutralizing antibodies are currently being developed. In this article, we note that human host cells sensitively respond to the spike protein to elicit cell signaling. Thus, it is important to be aware that the spike protein produced by the new COVID-19 vaccines may also affect the host cells. We should monitor the long-term consequences of these vaccines carefully, especially when they are administered to otherwise healthy individuals. Further investigations on the effects of the SARS-CoV-2 spike protein on human cells and appropriate experimental animal models are warranted.