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Wednesday, February 3, 2021

Walmart to begin administering coronavirus vaccines

 The nation's largest retailer will soon start administering coronavirus vaccines.

According to information posted online by Walmart, Arkansas is one of 22 states where trained pharmacists will provide COVID-19 vaccination shots.

"This is just another means of getting vaccines out into communities in which they're used to going to a Walmart," said Arkansas Gov. Asa Hutchinson.

Hutchinson said 60 stores in Arkansas will get vaccines. Currently, the list of participating locations has not been released. Hutchinson said 10,000 doses of vaccines from the federal government will be shipped to Walmart for use in Arkansas beginning Feb. 11.

The vaccines are in addition to those the state is already receiving, which, according to the governor, has increased 21% in the past 2 weeks.

"Walmart is good at a lot of things and that's moving inventory out and getting it into the stores and getting it out to the consumer," Hutchinson said. "We want that same excellence to be done in terms of our vaccines."

https://www.4029tv.com/article/walmart-to-begin-administering-coronavirus-vaccines/35399559

Astrazeneca looks to US data and a next-gen vaccine

 Data reported in a Lancet preprint this week suggesting that Astrazeneca’s Covid-19 vaccine has 76% efficacy, and reduces asymptomatic transmission of the virus by 67%, after a single shot are encouraging. But the disclosure of two hospitalisations for Covid-19 in this new cohort – the data concern the patients in the UK, Brazil and South Africa trials, whereas previous readouts concerned only the first two – is disquieting. These occurred within three weeks of the first dose and neither was judged “severe”, unlike three of the 22 hospitalisations in the control arm. And still lacking are decent data on AZD1222’s levels of protection in the over-65s; however, Astra’s Mene Pangalos said on a call today that this would arrive next month, as the US trial of AZD1222 reads out. A fifth of the 30,000 patients in this study are aged over 65. The company is already looking past this, however, and is working on a new version of the vaccine designed to be more active against new strains of the coronavirus, including the UK variant B117. Clinical trials in “the hundreds” of subjects are in the planning stage, and a next-generation vaccine could be on the shelves in autumn.

Phase III data on Astra's AZD1222 
  Covid-19-positiveSevere Covid-19 
Date reportedTrialsTime pointVaccinePboEfficacyVaccinePbo
Nov 23, 2020COV002 + COV00314 days after 2nd dose3010170%02
Feb 1, 2021COV002 + COV003 + COV00514 days after 2nd dose8424867%0*3**
Feb 1, 2021COV002 + COV003 + COV00522-90 days after single dose177176%--
*2 hospitalisations, neither severe. **22 hospitalisations, 3 severe. Source: Lancet preprint.

https://www.evaluate.com/vantage/articles/news/snippets/astrazeneca-looks-us-data-and-next-gen-vaccine

Vaxart's Not So Great Data From COVID-19 Oral Vaccine Study

 

  • Vaxart Inc (NASDAQ: VXRT) shares craters by more than half after reporting that neutralizing antibodies were not detected in volunteers after a single dose of its experimental oral COVID-19 vaccine candidate, VXA-CoV2-1, in a Phase 1 trial of 35 healthy adults. Researchers believe the antibodies play an important role in defending cells against the virus.
  • Vaxart scientists divided volunteers between ages 18 and 54 into three groups. The first received two low doses of the vaccine – 29 days apart, while the remaining groups received a single low or high dose.
  • According to the interim data, the vaccine generated a type of T-cell responsible for destroying virus-infected cells in about 75% of volunteers who received a single low or high dose.
  • On the safety front, no severe adverse events were reported, with side effects generally being mild. Volunteers reported common side effects such as headache and fatigue, and there was a “slight uptick” in the high-dose group of cases of loose stool, CNBC reports.
  • The company said it is now assessing antibody responses from second doses after antibodies were detected in nasal swab samples of two-dose volunteers.
  • The company said additional data from the Phase 1 trial would be presented today afternoon at a New York Academy of Sciences.

Retrained generic antibodies can recognize SARS-CoV-2

 The SARS-CoV-2, the new coronavirus behind the current pandemic, infects humans by binding its surface-exposed spike proteins to ACE2 receptors exposed on the cell membranes.

Upon a vaccination or a real infection, it takes several weeks before the immunity develops antibodies that can selectively bind to these spike proteins. Such antibody-labeled viruses are neutralized by the natural killer and T cells operated by the human immunity.

An alternative approach to train the immunity response is offered by researchers at the University of Illinois Chicago and California State University at Sacramento who have developed a novel strategy that redirects antibodies for other diseases existing in humans to the spike proteins of SARS-CoV-2.

In their study published by the Journal of Physical Chemistry Letters, the team proposes using peptide-based double-faced "booster" inhibitors, with one face binding to the spike proteins of SARS-CoV-2 and the other face binding to generic hepatitis B antibodies.

"Once the SARS-CoV-2 viruses become labeled by the hepatitis B antibodies via intermediate boosters, the viruses will be neutralized. This universal approach allows a dramatic shortening of the response time upon real infections, which can be critical in certain patients or conditions," said Petr Král, UIC professor of chemistry, physics, pharmaceutical sciences and chemical engineering, and senior author on the paper.

Král and Yanxiao Han, who recently earned a Ph.D. in chemistry at UIC and is first author on the paper, believe the study could provide guidance in the preparation of generic therapeutics against emerging pathogens with the combined advantages of small-protein and antibody therapies.

"The dramatic impact which novel viruses can have on humans could be fast mitigated in the absence of their vaccination if generic antibodies present within them are temporarily retrained to recognize these viruses," the researchers wrote.

In a study published last spring, Král and Han extracted different peptides from ACE2 that interact directly with the viral spike protein.

"We investigated potential COVID-19 therapeutics using computer simulations based on the X-ray crystal structure of the receptor-binding domain of SARS-CoV-2 when it is bound to ACE2," Král said. "Similar to our latest study, identifying these kinds of inhibitors could lead to new treatments to combat the coronavirus."

###

Co-author on the paper is Katherine McReynolds of California State University at Sacramento.

This work is supported by funding from the UIC Center for Clinical and Translational Science.

https://www.eurekalert.org/pub_releases/2021-02/uoia-rga020221.php

Israel data shows Pfizer jab stops illness, effect on transmissions unclear

 Initial data from Israel's coronavirus vaccination campaign shows the Pfizer/BioNTech jab protects against serious illness, but it is not yet clear whether it slows transmissions or spells progress toward achieving herd immunity, experts say.

The Jewish state is carrying out what is widely described as the world's fastest vaccination campaign per capita, watched closely by experts worldwide.

While many countries are struggling with procurement, Israel has made remarkable progress since launching inoculations in December.

So far, it has given the first of the two recommended doses of Pfizer jabs to roughly 35 percent of its nine-million population.

About 1.8 million have also received the second jab, mostly those over 60.

The health ministry announced that beginning Thursday, all Israelis aged 16 and over would be able to set an appointment to be vaccinated, dropping the age limit from its previous minimum of 35.

In a statement, the ministry stressed Wednesday that Israel's four health service providers should still focus their efforts on inoculating people aged 50 and over, as well as housebound Israelis.

Israel secured its substantial stock by paying above market price and by striking a data-sharing deal with Pfizer.

The agreement stipulates that Israel, which has one of the world's most sophisticated medical data systems, will share real-time information with Pfizer on the vaccine's impact, including on progress towards herd immunity.

Direct vs indirect protection

Ran Balicer, chairman of Israel's national expert panel on Covid-19, told AFP it was crucial to distinguish between the vaccine's two impacts.

The first is "the direct effect", of vaccinated people becoming "protected against symptomatic illness and severe disease", he said.

The second, "indirect effect" refers to the vaccine providing enough immunity to enough people that it forms an "epidemiological barrier" against transmission, he said.

Balicer, also the chief innovation officer at Clalit, Israel's largest health maintenance organisation (HMO), said the data shows the vaccine reduces serious illness, but the transmission question remained open.

Gabi Barbash, a prominent public health expert currently with the Weizmann Institute of Science, agreed.

"We do know that vaccines are decreasing the incidence of severe disease. That's it," he told AFP.

"We do not know whether the vaccines are minimising transmission."

Phase IV

In November, Pfizer announced that Phase III trials had showed its vaccine was 95 percent effective against the virus.

Given the gravity of the pandemic, it received regulatory approval through an accelerated trial process, which has made Israel's more comprehensive data even more valuable.

The country's Maccabi Institute of Innovation and Research, linked to an HMO of the same name, published a paper this week that it described as "the first and largest Phase IV study on the effectiveness of the (Pfizer-BioNTech) vaccine".

Clalit and Maccabi are two of Israel's four HMOs, which collectively provide healthcare to the entire population.

The HMOs are directly responsible for vaccinations and collecting data on their impact.

Maccabi compared the incidence of Covid-19 in the 12 days after individuals receiving their first Pfizer shot against incidence 13 to 24 days after the jab.

It found a 51 percent reduction in the incidence of lab confirmed infections in the latter period.

"Two weeks after the first dose you see a significant reduction in infection but it is not complete," Gabriel Chodick, co-author of the Maccabi report, told AFP.

Moreover, Israel is only testing those who present coronavirus symptoms, not a randomised sample of the entire vaccinated population.

It does not therefore have comprehensive data on the number of vaccinated people carrying the virus without symptoms.

Two jabs

Pfizer recommends administering its vaccine in two doses, three weeks apart.

Israel has enough stocks to follow these recommendations, meaning it does not have data on whether the protective effect from just one jab increases after 24 days in the absence of a second jab.

Maccabi has also released preliminary data on the second jab's impact.

It showed that out of 248,000 people studied one week after receiving their second injection, only 66 mild  infections were registered.

While those figures point towards near-total protection, Maccabi has stressed this data has not been fully analysed.

Despite its vaccination campaign, Israel has continued to register daily caseloads above 5,000, despite a nationwide lockdown in place since December 27.

But compliance with and enforcement of the lockdown has been uneven, notably among ultra-Orthodox Jews who have persistently flouted public safety rules throughout the pandemic.

"If you look at the number of new identified positive corona cases per day, it has not decreased for the last month and half," Barbash said.

"So is it because the lockdown is not a (real) lockdown, or is it because the  is not minimising transmission? No one can tell that."

https://medicalxpress.com/news/2021-02-israel-pfizer-jab-illness-effect.html

Potential antiviral treatment for COVID-19, other viruses, found

 Researchers from the University of Nottingham have discovered a novel antiviral property of a drug that could have major implications in how future epidemics / pandemics—including COVID-19—are managed.

The study, published in Viruses, shows that thapsigargin is a promising broad spectrum antiviral, highly effective against COVID-19 virus (SARS-CoV-2), a common cold ,  (RSV) and the influenza A virus.

Given that acute respiratory virus infections caused by different viruses are clinically indistinguishable on presentation, an effective broad-spectrum that can target different virus types at the same time could significantly improve clinical management. An antiviral of this type could potentially be made available for community use to control active infection and its spread.

The study is a collaborative project led by Professor Kin-Chow Chang and experts at the University of Nottingham (Schools of Veterinary Medicine and Sciences, Biosciences, Pharmacy, Medicine, and Chemistry), and colleagues at the Animal and Plant Health Agency (APHA), China Agricultural University and the Pirbright Institute.

In this ground-breaking study, the team of experts found that the plant-derived antiviral, at small doses, triggers a highly effective broad-spectrum host-centred antiviral innate immune response against three major types of human respiratory viruses—including COVID-19.

The key features based on cell and animal studies, which make thapsigargin a promising antiviral are that it is:

  • effective against viral infection when used before or during active infection
  • able to prevent a virus from making new copies of itself in cells for at least 48 hours after a single 30-minute exposure.
  • stable in acidic pH, as found in the stomach, and therefore can be taken orally, so could be administered without the need for injections or hospital admission.
  • not sensitive to virus resistance.
  • at least several hundred-fold more effective than current antiviral options.
  • just as effective in blocking combined infection with coronavirus and influenza A virus as in single-virus infection.
  • safe as an antiviral (a derivative of thapsigargin has been tested in prostate cancer).

Professor Chang said: "Whilst we are still at the early stages of research into this antiviral and its impact on how viruses such as COVID-19 can be treated, these findings are hugely significant.

"The current pandemic highlights the need for effective antivirals to treat active infections, as well as vaccines, to prevent the . Given that future pandemics are likely to be of animal origin, where animal to human (zoonotic) and reverse zoonotic (human to animal) spread take place, a new generation of antivirals, such as thapsigargin, could play a key role in the control and treatment of important  in both humans and animals."

Indeed, influenza virus, coronavirus and RSV are global pathogens of humans as well as . Thapsigargin represents a lead compound in the development of a new generation of powerful host-centred antivirals (as opposed to conventional antiviral drugs that directly target viruses) that could even be adopted in a holistic "One Health" approach to control human and animal .

Professor Chang adds: "Although more testing is clearly needed, current findings strongly indicate that thapsigargin and its derivatives are promising antiviral treatments against COVID-19 and influenza , and have the potential to defend us against the next Disease X pandemic."

https://medicalxpress.com/news/2021-02-scientists-uncover-potential-antiviral-treatment.html

Piper Sandler Upgrades Jazz Pharmaceuticals (JAZZ) to Overweight

 

Following GWPH Acquisition Deal

https://www.streetinsider.com/Upgrades/Piper+Sandler+Upgrades+Jazz+Pharmaceuticals+%28JAZZ%29+to+Overweight%2C+Following+GWPH+Acquisition+Deal/17909910.html