Thursday, July 21, 2022

Study: Pfizer-BioNTech and AstraZeneca vaccines offer high protection against severe COVID-19

Protection against severe COVID-19 by two doses of Pfizer-BioNTech and AstraZeneca COVID-19 vaccines remained high up to six months after second doses, according to new research which analyzed NHS health record data on over seven million adults.

The University of Bristol-led study published in The BMJ found protection in older adults aged over 65 years, and in clinically vulnerable adults.

Researchers from Bristol Medical School sought to investigate how quickly vaccine effectiveness waned over time in adults without prior SARS-CoV-2 infection and who received two doses of BNT162b2 (Pfizer-BioNTech) or ChAdOx1 (AstraZeneca) COVID-19 vaccine compared with unvaccinated individuals.

Method and findings

Using linked GP, hospital, and COVID-19 records on 1,951,866 and 3,219,349 adults who had received two doses of BNT162b2 and ChAdOx1, respectively and 2,422,980 unvaccinated adults, researchers were able to provide a clearer picture of vaccine effectiveness against COVID-19 hospital admission, COVID-19 death, and positive SARS-CoV-2 test.

Rates of COVID-19 hospital admission and COVID-19 death were substantially lower among vaccinated than unvaccinated adults up to six months after their second dose.

Vaccine effectiveness against these events was found to be at least 80% for BNT162b2, and at least 75% for ChAdOx1. However, waning vaccine effectiveness against infection with SARS-CoV-2 meant that rates in vaccinated individuals were similar to or higher than in unvaccinated individuals by six months after the second dose.

Protection still high after 6 months

Dr Elsie Horne, Senior Research Associate in Medical Statistics and Health Data Science in Bristol Medical School, Population Health Sciences (PHS) and the study’s lead author, said, “Until now there has been limited and conflicting evidence relating to the rate of waning following second dose of COVID-19 vaccines, whether it extends to severe COVID-19, and whether the rate differs according to age and clinical vulnerability.

“Although we found that protection against severe COVID-19 provided by two doses of vaccine wanes over time, the very high initial protection means that, despite waning, protection remains high six months after the second dose. This finding was consistent across all adults, including older adults and those who are at risk of severe COVID-19.”

Jonathan Sterne, Professor of Medical Statistics and Epidemiology in Bristol Medical School PHS, Director of the National Institute for Health and Care Research Bristol Biomedical Research Centre (NIHR Bristol BRC), Director of Health Data Research UK (HDR UK) South-West and co-author, added, “We found that the rate at which vaccine effectiveness waned was consistent across subgroups defined by age and clinical vulnerability.

Studying how long COVID-19 vaccines remain effective continues to be important to scheduling and targeting of booster vaccinations.”

The researchers now plan to lead a follow-up study looking at vaccine effectiveness to one year post-second dose and into the era of the Omicron variant. They are also investigating the rate of waning in vulnerable clinical subgroups, such as those with chronic kidney disease and with cancer.

The study was supported by two COVID-19 National Core Studies (NCS) programmes: COVID-19 Longitudinal Health and Wellbeing and COVID-19 Data and Connectivity; Asthma UK; NIHR (National Institute for Health and Care Research) and Wellcome. TPP provided technical expertise and infrastructure pro bono in the context of a national emergency.

REFERENCE:

Horne EMF...Sterne JAC. Waning effectiveness of BNT162b2 and ChAdOx1 covid-19 vaccines over six months since second dose: OpenSAFELY cohort study using linked electronic health records. BMJ July 20, 2022; 378 DOI: 10.1136/bmj-2022-071249

Wednesday, July 6, 2022

Hebrew U Startup 'Viroblock' is Developing New Anti-Viral Medication

A startup company founded by Hebrew University of Jerusalem (HU) has developed a new medication that targets common viruses.

ViroBlock announced June 6 that it has developed a new drug platform for rapidly generating anti-viral drugs that target proteins common to all viruses, such as current and future COVID-19 variants, Influenza, Zika, West Nile, Hepatitis and future threats.

Working on a drug to fight COVID-19


"Currently, there are no efficient, validated platforms for rapidly generating anti-viral drugs," says ViroBlock CEO and Founder Isaiah (Shy) Arkin, who is also an HU professor of biological chemistry in the Alexander Silberman Institute of Life Sciences.

"Scientists must develop new agents and a customized approach to target every new virus, without the ability to predict how that virus will develop resistance.

ViroBlock is working on a promising drug candidate for COVID-19 using an approach that can be duplicated with most other important viruses."

Numerous viruses targeted


According to a new study conducted by pharma research company Evotec, ViroBlock’s new technology platform demonstrated the potential to rapidly provide solutions for treating current and emerging viral threats, including COVID-19 and variants, influenza, Zika, West Nile, and Hepatitis B.

The study showed that channel blockers it identified could protect cells from viral-induced death alongside dramatically lowering the amount of viral progeny.

How it works


ViroBlock's antiviral drug candidates inhibit two targets in the virus: the E (envelope) protein and the 3a protein.

The E protein is an ion channel, a type of protein family expressed by virtually all living cells that because of its structure has served as a frequent target for pharmaceutical point interventions.

For example, while the spike proteins of SARS-CoV-2 and SARS-CoV-1 (the 2003 virus) are only about 75 percent identical, their E proteins are roughly 95 percent alike. This means the ViroBlock drugs would likely remain effective even when the virus mutates.

"With our propriety technology, ViroBlock can identify targets in a new viral threat (or variant), develop inhibitors against it, and determine the resistance potential of the virus against the new drug, all at an unprecedented pace," Arkin says.

Testing on humans is next


The next phase of clinical trials will test the efficacy of this anti-viral approach for humans.

The company also has drugs in the pipeline produced by the platform currently being tested that could be effective against other viruses.

ViroBlock was founded in 2020 by Yissum, the Hebrew University technology transfer company.