Coronavirus Breaking News

The coronavirus disease COVID-19 is currently reaching pandemic levels in various countries.

May 28, 2021 • 10:32 am CDT

The U.S. HHS issued a Public Health Emergency notice on May 26, 2021, regarding COVID-19 monoclonal antibody treatments currently authorized for emergency use in certain patients with COVID-19.

Results from in vitro assays used to assess the susceptibility of viral variants to particular monoclonal antibodies suggest that bamlanivimab and etesevimab administered together are not active against either the P.1 or B.1.351 variants.

And the US Centers for Disease Control and Prevention has identified that the combined frequency of the P.1 variant now exceeds 10% in certain states.

Therefore, the distribution of bamlanivimab and etesevimab to Illinois, Massachusetts, Arizona, California, Florida, Indiana, Oregon, and Washington has been paused.

REGEN-COV is an alternative monoclonal antibody therapy currently authorized for the same use as bamlanivimab and etesevimab administered together and, based on similarities in vitro assay data currently available, REGEN-COV is likely to retain activity against the P.1 and B.1.351 variants.

All treatment delivery sites can continue ordering REGEN-COV from the authorized distributor by following the existing ordering and reporting procedures. Please see the updates for additional information.

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May 26, 2021 • 6:30 pm CDT

The Australian government announced on Twitter that COVID-19 lockdown restrictions had been announced effective late on May 26, 2021.

This action is in response to several positive COVID-19 cases in the city of Melbourne's suburbs.

The government indicated it is shipping additional Pfizer and AstraZeneca COVID-19 vaccines into the Melbourne area asap.

According to local media, Victoria's contact tracing program was criticized by the Australian Medical Association for incorrectly listing virus exposure sites.

May 26, 2021 • 5:55 pm CDT

According to a new study published in the JAMA Network Open on May 25, 2021, throughout the COVID-19 pandemic, healthcare providers have seen evidence that men with COVID-19 fare worse, on average, than women.

One theory is that hormonal differences between men and women may make men more susceptible to severe COVID-19.

And since men have much more testosterone than women, some scientists have speculated that high testosterone levels may be to blame.

However, a study from Washington University School of Medicine researchers suggests that, among men, the opposite may be true.

In a cohort study of 152 patients with COVID-19, including 143 patients hospitalized, testosterone concentrations at presentation and on day 3 were inversely associated with disease severity and circulating inflammatory cytokine concentrations in men but not in women.

This study could not prove that low testosterone is a cause of severe COVID-19. And low levels could serve as a marker of some other causal factors.

Still, the researchers urge caution with ongoing clinical trials investigating hormonal therapies that block or lower testosterone or increase estrogen treatment for men with COVID-19.

May 26, 2021 • 1:53 pm CDT

According to a study published ahead of the June 2021 print issue, based on the number of dentists with confirmed or probable COVID-19 infections, the cumulative infection rate for U.S. dentists is 2.6%.

By comparison, in June 2020, the cumulative COVID-19 prevalence rate for other U.S. health professionals ranged from 3.3% (Chicago hospital physicians) to 35.3% (U.S.-based emergency medical services).

“We’re pleased to see that dentists have demonstrated the continued low monthly incidence during the study period,” commented American Dental Association (ADA) Science and Research Institute CEO Marcelo Araujo, D.D.S., M.S., Ph.D., the senior author of the report published on May 24, 2021.

Dr. Araujo added, “This study shows high rates of pre-appointment screening of patients and appropriate infection control measures throughout the study period, demonstrating that adhering to rigorous protocols for enhanced infection control helps protect their patients, their dental team, and themselves.”

The Journal of the ADA study is based on data collected June 9 - Nov. 13, 2020. For more information on COVID-19 and dental visits, visit MouthHealthy.org.

The study authors plan future research projects on the barriers and facilitators to wearing Personal Protective Equipment (PPE) according to CDC recommendations and levels of protection against COVID-19 provided by different levels of PPE use and infection control procedures.

The ADA was founded in Niagara Falls, New York, during 1859.

May 26, 2021 • 12:54 pm CDT

The U.S. FDA's Center for Devices and Radiological Health has issued a new report on May 25, 2021, that describes the approaches used by the South Korean government to address COVID-19, particularly regarding the development, authorization.

South Korea’s approach was based on lessons they learned from a deadly Middle Eastern Respiratory Syndrome outbreak in 2015 and the steps they took before the COVID-19 pandemic hit.

First, the government invested in the commercial development of diagnostic testing technology. Since 2017, the Ministry of Science and Information and Communications Technology has invested almost 25 million U.S. dollars in infectious disease diagnosis technology.

As a result of these investments, a subset of South Korean commercial manufacturers was well-positioned to develop and manufacture tests quickly.

Second, the government designed an emergency use authorization pathway modeled on the system used in the U.S.

Third, the South Korean legislature amended the Infectious Disease Prevention and Control Act of Korea in 2015 to allow relevant authorities to collect personal data on confirmed and suspected cases of infection during an infectious disease emergency.

In early April 2020, numerous sources worldwide declared South Korea’s response strategy had successfully "flattened the curve" of COVID-19.

As South Korea's experience may be informative for future considerations, the FDA reviewed the information, including reports in the press and information made publicly available by the South Korean government about their COVID-19 response strategy.

The FDA recognizes different approaches may work for different countries. This report does not recommend what approaches could or should be adopted in the USA for emerging infectious diseases.

May 25, 2021 • 5:50 am CDT

A Northwestern University Medicine study of placentas from women who received a COVID-19 vaccine during pregnancy found no evidence of injury.

Most women in this limited study received either Moderna or Pfizer-BioNTech mRNA vaccines during their third trimester.

The study was published May 11, 2021, in the journal Obstetrics & Gynecology. To the authors’ knowledge, it is the first study to examine the impact of the COVID vaccines on the placenta.

The study authors collected placentas from 84 vaccinated patients and 116 unvaccinated patients who delivered at Prentice Women’s Hospital in Chicago, Illinois, and pathologically examined the whole of the placenta and microscopically following the birth.

The placenta is the first organ that forms during pregnancy. It performs duties for most of the fetus’ organs while they’re still forming, such as providing oxygen while the lungs develop and nutrition while the gut is forming.

Additionally, the placenta manages hormones and the immune system and tells the mother’s body to welcome and nurture the fetus rather than reject it as a foreign intruder.

The scientists also looked for abnormal blood flow between the mother and fetus and problems with fetal blood flow – both of which have been reported in pregnant patients who have tested positive for COVID.

The rate of these injuries was the same in the vaccinated patients as for control patients.

The Northwestern scientists also examined the placentas for chronic histiocytic intervillositis, a complication that can happen if the placenta is infected, in this case, by SARS-CoV-2.

Although this study did not find any cases in vaccinated patients, it's a rare condition requiring a larger sample size (1,000 patients) to differentiate between vaccinated and unvaccinated patients.

The study was funded by The Friends of Prentice, the Stanley Manne Children’s Research Institute, the National Institute of Biomedical Imaging and Bioengineering, and the National Institute of Allergy and Infectious Diseases.

May 24, 2021 • 4:49 pm CDT

A new study published in the journal Nature by researchers associated with Washington University School of Medicine found 'that SARS-CoV-2 infection induces a robust antigen-specific, long-lived humoral immune response in humans.'

Published on May 24, 2021, this study focused on long-lived bone marrow plasma cells (BMPCs), a persistent and essential source of protective antibodies.

It has been reported that anti-SARS-CoV-2 serum antibodies experience rapid decay in the first few months after infection, raising concerns that long-lived BMPCs may not be generated and humoral immunity against this virus may be short-lived.

These researchers demonstrated that in patients who experienced mild infections (n=77), serum anti-SARS-CoV-2 spike (S) antibodies declined rapidly in the first 4 months after infection and then more gradually over the following 7 months, remaining detectable at least 11 months after infection.

Anti-S antibody titers correlated with the frequency of S-specific BMPCs obtained from bone marrow aspirates of 18 SARS-CoV-2 convalescent patients 7 to 8 months after infection.

S-specific BMPCs were not detected in aspirates from 11 healthy subjects with no history of SARS-CoV-2 infection.

The researchers found that S-binding BMPCs are quiescent, indicating that they are part of a long-lived compartment.

Consistently, circulating resting memory B cells directed against the S protein were detected in the convalescent individuals.

Overall, we show that SARS-CoV-2 infection induces a robust antigen-specific, long-lived humoral immune response in humans.

This is an unedited manuscript that has been accepted for publication. Nature Research is providing this early version of the manuscript as a service to our authors and readers. No industry conflicts were disclosed. Correspondence to Ali H. Ellebedy.

May 24, 2021 • 1:33 pm CDT

The Moscow-based Russian Direct Investment Fund (RDIF) announced data from a study conducted by the Institute of Virology of the National University of Cordoba located in Argentina and the authorities of Cordoba, which confirm the neutralizing effect of the two-component Sputnik V vaccine against the Brazilian strain of SARS-CoV-2 beta coronavirus, first identified in the city of Manaus.

In particular, the study confirmed 99.65% of individuals developed IgG antibodies to coronavirus on the 42nd day after receiving the second injection of the Sputnik V vaccine.

And 85.5% of individuals developed IgG antibodies to coronavirus on the 14th day after receiving the first injection of Sputnik V.

The RDIF recently announced the availability of the Sputnik LIght vaccine, which is a single-dose version.

The RDIF was founded in 2011 to invest in the equity capital of companies primarily in Russia, together with leading foreign financial and strategic investors.

May 23, 2021 • 8:49 am CDT

Japan's Defense Ministry confirmed it administered COVID-19 Vaccine Moderna Intramuscular Injection (TAK-919) among Self-Defense Forces (SDF) members, reported Kyodo News on May 23, 2021.

This is the first confirmed use of Moderna's mRNA vaccine in Japan.

SDF healthcare providers and private nurses are being scheduled to offer vaccinations in Tokyo and Osaka on May 24th.

This is important since the Japan Times reported today a government spokesman discussed the possibility of extending the current State of Emergency in Tokyo, Osaka, and other prefectures beyond the May 31st expiration date.

Previously, Takeda Pharmaceutical Company announced that Japan's Ministry of Health, Labour and Welfare (MHLW) granted special approval for the emergency use of Moderna’s vaccine known in Japan as COVID-19 Vaccine Moderna Intramuscular Injection.

“This is an important step in Takeda’s support of Japan’s pandemic response,” commented Rajeev Venkayya, president of the Global Vaccine Business Unit at Takeda, in a press statement.

“Moderna’s vaccine demonstrated an excellent safety profile, and we are excited to make it available to the Japanese population.”

The approval results from a three-way agreement announced in October 2020 with Moderna and Japan’s MHLW to distribute 50 million doses of the TAK-919 vaccine in Japan in the first half of 2021.

Takeda Pharmaceutical is a global, values-based, R&D-driven biopharmaceutical leader headquartered in Osaka, Japan.

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May 21, 2021 • 10:50 am CDT

Geneva-based Gavi, the Vaccine Alliance, announced on May 21, 2021, that it had signed a purchase agreement with Johnson & Johnson (J&J) for its single-dose Janssen COVID-19 vaccine.

The agreement is for a commitment to purchase 200 million doses on behalf of the COVAX Facility, with the goal of them being supplied to Facility participants in 2021.

Gavi stated it 'will continue to assess its needs and remain in discussions with Johnson & Johnson on the potential supply of 300 million additional doses in 2022.'

The Janssen COVID-19 (Ad26.COV2.S) single-shot experimental vaccine leverages Janssen's AdVac and PER.C6® technologies. Janssen’s AdVac® vectors are based on a specific type of adenovirus, which has been genetically modified so that it can no longer replicate in humans and cause disease.

Adenoviruses are a group of viruses that can cause the common cold, says the U.S. CDC.

Dr. Seth Berkley, the CEO of Gavi, commented in a related press release, “As a one-dose vaccine, the J&J vaccine has particular relevance for places with difficult infrastructure, making it a very important addition to the portfolio.”

Gavi is a public-private partnership that helps vaccinate half the world’s children against some of the world’s deadliest diseases. Since its inception in 2000, Gavi has helped to immunize over 822 million children and prevented more than 14 million deaths in 73 lower-income countries.

May 21, 2021 • 8:37 am CDT

BioNTech Europe GmbH confirmed on May 20, 2021, it has agreed with the Republic of Turkey’s Ministry of Health to supply 60 million additional doses of the companies’ mRNA COVID-19 vaccine, with an option for an additional 30 million doses.

This second supply agreement brings the total number of Cominraty vaccine doses to Turkey to up to 120 million, all of which will be delivered in 2021.

“We are hopeful that this agreement will further boost Turkey’s COVID-19 vaccination drive. Pfizer is committed to contributing to public health in Turkey and very proud to have a global partner such as BioNTech in the global fight against the pandemic,” commented M. Cem Açık, Pfizer Country Manager Turkey, in a press statement.

The Comirnaty vaccine, based on BioNTech’s proprietary mRNA technology, was developed by BioNTech and Pfizer.

Do not administer the Pfizer-BioNTech COVID-19 vaccine to individuals with a known history of a severe allergic reaction to any component of the Pfizer-BioNTech COVID-19 vaccine.

Germany-based BioNTech SE is the Marketing Authorization Holder in the European Union and the holder of emergency use authorizations or equivalent in the United States (jointly with Pfizer), United Kingdom, Canada, and other countries in advance of a planned application for full marketing authorizations in these countries.

May 21, 2021 • 6:15 am CDT

The COVID-19 Vaccine Moderna Intramuscular Injection (TAK-919) was granted Special Approval in Japan by the Ministry of Health, Labour, and Welfare (MHLW) on May 21, 2021.

Osaka-based Takeda Pharmaceutical Company Limited announced the approval was based on positive clinical data from Takeda’s Phase 1/2 immunogenicity and safety clinical trial of Moderna’s COVID-19 vaccine in Japan.

The approval results from a three-way agreement announced on October 29, 2020, between Takeda, Moderna, and the Government of Japan’s MHLW to distribute 50 million doses of TAK-919 in Japan in the first half of 2021.

“This is an important step in Takeda’s support of Japan’s pandemic response,” stated Rajeev Venkayya, president of the Global Vaccine Business Unit at Takeda, in a related press statement.

“Moderna’s vaccine has demonstrated an excellent safety and effectiveness profile to date, and we are excited to make it available to the Japanese population.”

The COVID-19 Vaccine Moderna (mRNA-1273) is an mRNA vaccine targeted against the SARS-CoV-2 coronavirus encoding for a prefusion stabilized form of the Spike (S) protein.

Takeda's employees are committed to improving the quality of life for patients and working with our healthcare partners in approximately 80 countries. For more information, visit https://www.takeda.com.

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May 20, 2021 • 5:35 pm CDT

The European Centre for Disease Prevention and Control (ECDC) launched a digital dashboard that overviews the proportion of SARS-CoV-2 variants of concern and variants of interest in Europe.

A variant has one or more mutations that differentiate it from other variants in circulation. As expected, multiple variants of the SARS-CoV-2 beta coronavirus have been documented throughout the COVID-19 pandemic.

Where data are available from more than one source for a country, the source used is the one with the highest number of sequences in the last two weeks. This new dashboard is updated every Thursday afternoon.

The full-screen version is available at this ECDC link.

On May 17, 2021, a US government interagency group developed a Variant Classification scheme that defines three classes of SARS-CoV-2 variants:

  • Variant of Interest
  • Variant of Concern
  • Variant of High Consequence

Current SARS-CoV-2 variants in the USA are being monitored and characterized. They are listed on this CDC webpage.

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May 20, 2021 • 5:12 pm CDT

As the COVID-19 vaccine rollout ramps up, the risks and benefits of immunization for pregnant and breastfeeding women remain largely unknown because the initial COVID-19 vaccine clinical trials didn’t include these populations.

To fill the knowledge gap, Candian researchers are launching a COVID-19 vaccine registry and survey. They will collect real-time data on the impact of immunization on pregnant women and breastfeeding mothers across the country.

Researchers will monitor the attitudes, effectiveness, and safety of the various COVID-19 vaccines for pregnant and lactating women through this registry and survey. Participants do not have to have already received a COVID-19 vaccine, nor are they required to be vaccinated.

This project, funded by the Public Health Agency of Canada through the Vaccine Surveillance Reference Group and the COVID-19 Immunity Task Force, is being conducted in partnership with vaccine surveillance efforts across Canada.

To participate in the registry and survey, visit the Reproductive Infectious Diseases Program website.

The University of British Columbia is located in Vancouver, BC.

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May 19, 2021 • 7:09 pm CDT

The United Arab Emirates (UAE) announced it would offer a third dose of the Sinopharm COVID-19 vaccine six months after their initial two-dose regimen was administered. This announcement reported by SCMP on May 19, 2021, appears to make the UAE the first country to introduce the COVID-19 booster dose formally.

The UAE became the first country to manufacture its own local version of the Sinopharm vaccine, Hayat-Vax.

Sinopharm's COVID-19 (BBIBP-CorV) is an inactivated vaccine made of virus particles grown in culture and lack disease-producing capability. This vaccine works by teaching the immune system to make antibodies against the SARS-CoV-2 beta coronavirus.

On May 18, 2021, the UAE's Ministry of Health and Prevention (MoHAP) announced that it conducted 202,184 additional COVID-19 tests over the past 24 hours.

In a statement, the Ministry stressed its aim to continue expanding the scope of testing nationwide to facilitate the early detection of coronavirus cases and carry out the necessary treatment. As part of its intensified testing campaign, the MoHAP announced 1,270 new coronavirus cases.

According to the Ministry, the infected individuals are from various nationalities, are stable, and receive the necessary care.

The MoHAP also announced four deaths due to COVID-19 complications, bringing the total number of deaths in the country to 1,637 during the pandemic.

Locate in Dubai, the Ministry's mission is 'To enhance community health by providing comprehensive, innovative, and fair healthcare services as per international standards, and performing its role as a regulator and supervisor of the healthcare sector through a modern and integrated health legislative system.'