Coronavirus Breaking News

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

Mar 24, 2023 • 4:34 am CDT
Salt Lake City airport March 24, 2023

Salt Lake County Health Department (SLCoHD) today announced a case of measles in a local unvaccinated resident.

This is the first case of measles in Utah since 2017.

Utah joins Kentucky and Ohio in reporting recent measles cases.

The SLCHD stated in a press release on March 23, 2023, the public is at minimal risk of illness due to this case related to international travel.

The infected person's exposure is limited to healthcare settings and the person's family members.

Anyone vaccinated against measles is protected even if they may have been exposed. This means they do not need to take any action.

And contact tracers notified people who may have been exposed and advised unvaccinated contacts to get vaccinated immediately.

Receiving a measles vaccine after exposure can prevent illness if administered within 72 hours.

Furthermore, the U.S. Centers for Disease Control and Prevention (CDC) says no specific antiviral treatment exists for the measles virus.

However, research indicates vitamin A deficiency is a recognized risk factor for severe measles infections. Therefore, at-risk children diagnosed with measles should receive two vitamin A supplements 24 hours apart.

"Measles is a vaccine-preventable disease," commented Dr. Angela Dunn, SLCoHD executive director.

"While over 90% of children in Utah schools and childcare facilities are adequately vaccinated, there are still people in our community who are not protected," continued Dr. Dunn.

"Being fully vaccinated against measles does more than just protect the person who receives the vaccination; it also protects their family and friends, including children who may be too young to be vaccinated, and it helps limit the spread of disease in the community."

Furthermore, the CDC recommends protecting international travelers with an MMR vaccine before visiting measles outbreak communities in countries such as India.

Various measles vaccines are available at most health clinics and community pharmacies in the U.S.

Mar 23, 2023 • 5:49 pm CDT
WHO Influenza Report 441 March 20, 2023

The World Health Organization (WHO) recently published Influenza Update N° 441, confirming influenza activity continued to decrease following the peak in late 2022.

In the countries of North America, most indicators of influenza activity were at levels typically observed towards the end of the flu season.

Influenza A viruses predominated overall, with influenza A(H3N2) accounting for most subtyped influenza A viruses in the United States, whereas influenza A and B viruses circulated similarly in Canada.

And in Europe, out of 39 countries, 17 reported high or moderate intensity, and over half continued to report widespread activity.

Overall, influenza B viruses were predominated in both sentinel and non-sentinel surveillance as all subregions experienced a wave of influenza B activity after an initial influenza A surge.

While the Northern Hemishpere flu season is ending, the WHO's data on March 20, 2023, indicates the Southern Hemishpere is just starting.

For international travelers, the means another flu shot may be needed when visiting countries such as Brazil, Peru, or Argentina later this year.

Community pharmacies in the U.S. generally offer influenza vaccines throughout the year.

Mar 23, 2023 • 7:34 am CDT
U.S. CDC polio outbreak map March 22, 2023

The U.S. Centers for Disease Control and Prevention (CDC) today announced it had expanded its Alert - Level 2, Practice Enhanced Precautions global polio travel notice.

As of March 22, 2023, the CDC increased the number of countries listed.

Furthermore, the CDC stated that before traveling to any destination listed, adults who previously completed the full, routine polio vaccine series receive a single, lifetime booster dose.

Previously, the World Health Organization confirmed the spread of poliovirus remained a Public Health Emergency of International Concern.

Recently, the New York State Department of Health announced that New Yorkers intending to visit Israel and other countries with circulating poliovirus should ensure they are fully immunized against polio.

In the U.S., CDC updated the pediatric and adult polio vaccination schedules in February 2023.

The inactivated polio vaccine (IPV) is recommended within four weeks of travel. Various IPV-containing vaccines are available at most health clinics and community pharmacies.

Mar 23, 2023 • 7:05 am CDT
CDC Travel Advisory Tanzania March 21, 2023

The U.S. Centers for Disease Control and Prevention (CDC) today announced the United Republic of Tanzania declared an outbreak of Marburg virus disease (MVD), with confirmed cases reported in the Kagera Region.

Other MVD outbreaks in Africa have been confirmed in 2023.

MVD is a viral hemorrhagic fever, with symptoms including fever, chills, headache, muscle pain, rash, sore throat, diarrhea, vomiting, stomach pain, chest pain, and unexplained bleeding or bruising.

Infection with the Marburg virus is often fatal, as there is no specific treatment, says the CDC.

As of March 21, 2023, the CDC's Watch - Level 1, Practice Usual Precautions notices advises visitors should separate themselves from others and seek medical care immediately if they develop fever, chills, muscle pain, rash, sore throat, diarrhea, weakness, vomiting, stomach pain, or unexplained bleeding or bruising during or after travel (up to 21 days).

As of March 23, 2023, no MVD preventive vaccines are authorized.

Mar 22, 2023 • 4:42 pm CDT
by Silvia P.

The National Veterinary Services Laboratories (NVSL) today announced the presence of Highly Pathogenic Avian Influenza (HPAI) in a striped skunk recovered from Carson County, located east of Amarillo in the Texas panhandle.

As of March 21, 2023, this is the first confirmed case of HPAI in mammals in Texas.

HPAI is a highly contagious virus that transmits efficiently among wild and domestic birds. The virus can spread directly between animals and indirectly through environmental contamination.

Since the H5 clade 2.3.4.4b. appeared in North America in January 2022, over 6,000 H5N1 detections in wild birds, by 47 states (14 states within 30 days), leading to the loss of over 58 million birds as of March 17, 2023.

For mammals, current data shows transmission occurs primarily through the consumption of infected animal carcasses, though mammal-to-mammal transmission does not appear sustainable.

Other mammal species confirmed with HPAI in the U.S., Canada, Central Ameria, and South America include foxes, raccoons, bobcats, opossums, mountain lions, and black bears. 

Because of the ease of transmission, the TPWD recommends that wildlife rehabilitators also remain cautious when intaking wild animals with clinical signs consistent with HPAI and consider quarantining animals to limit the potential for HPAI exposures to other animals within the facility.

Currently, the transmission risk of avian influenza from infected birds to people remains low.

But the public should take basic protective measures, such as wearing gloves, face masks, and handwashing if contact with wild animals cannot be avoided.

Furthermore, the U.S. government has approved avian influenza vaccines should human-to-human transmission occur since the annual flu shot is not effective against this type of influenza.

Mar 22, 2023 • 2:34 pm CDT
WHO cholera outbreaks March 2023

The world is facing an upsurge in Cholera, even touching countries that have not had the disease in decades, announced the World Health Organization (WHO) on World Water Day.

Years of progress against this age-old disease have disappeared, stated the WHO on March 22, 2023. In the past months, the world has seen a resurgence of Cholera.

Last year, as many as 30 countries experienced outbreaks, and we continue to see a worrying geographic spread into 2023. 

While the situation is unprecedented, the lesson to draw is not new: safe drinking water, sanitation, and hygiene are the only long-term and sustainable solutions to ending this cholera emergency and preventing future ones.

The global cholera situation is concerning, but the historic United Nations Water Conference began in New York. The Global Task Force for Cholera Control appeals to countries and the international community to channel that concern toward concrete action.

Nearly all cholera cases reported in the U.S. are acquired during international travel, says the U.S. Centers for Disease Control and Prevention (CDC).

For example, the CDC confirmed eight travelers infected with Cholera arrived in the U.S. from Pakistan, Iraq, and Bangladesh in 2022.

In 2023, various countries have confirmed cholera outbreaks.

As of March 22, 2023, cholera vaccines, such as Valneva SE's DUKORAL® oral, inactivated Cholera, and ETEC Diarrhea vaccine, have been approved and are available in certain countries.

Mar 22, 2023 • 2:07 pm CDT
from Pixabay

A recent article published by eBioMedicine discussed how the Zika virus leads to olfactory disorders in mice by targeting olfactory ensheathing cells.

On February 3, 2023, this article confirmed Zika virus (ZIKV) is an emerging arbovirus of the genus flavivirus associated with congenital Zika syndrome (CZS) in newborns.

Clinical symptoms, including intellectual disability, speech delay, coordination or movement problems, and hearing and vision loss, have been well-documented in children with CZS.

However, whether ZIKV can invade the olfactory system (ability to detect odors) and lead to post-viral olfactory dysfunction (PVOD) remains unknown.

These researchers demonstrated that neonatal mice infected with ZIKV suffer transient olfactory dysfunction when they reach puberty.

Moreover, ZIKV mainly targets olfactory ensheathing cells (OECs) and exhibits broad cellular tropism colocalizing with small populations of mature/immature olfactory sensory neurons (mOSNs/iOSNs), sustentacular cells and horizontal basal cells in the olfactory mucosa (OM) of immunodeficient AG6 mice.

ZIKV infection induces strong antiviral immune responses in the olfactory mucosa and olfactory bulb tissues, resulting in the upregulation of proinflammatory cytokines/chemokines and genes related to the antiviral response. 

'Our results demonstrate that the olfactory system represents a significant target for ZIKV infection and that PVOD may be neglected in CZS patients,' concluded these researchers.

The authors declared that they have no conflict of interest.

Mar 22, 2023 • 11:15 am CDT
by Harald Matern

The U.S. Centers for Disease Control and Prevention (CDC) published Dispatch, Volume 26, Number 12, on November 19, 2020; Susceptibility of Raccoon Dogs for Experimental SARS-CoV-2 Infection, which is inserted below:

Raccoon dogs might have been intermediate hosts for severe acute respiratory syndrome coronavirus (SARS-CoV-1) in 2002–2004. 

Our experimental study demonstrates that raccoon dogs are susceptible to SARS-CoV-2 infection. However, in our research, raccoon dogs had only subtle clinical signs.

Additionally, we found evidence of viral replication and tissue lesions in only the nasal conchae, which can transmit the virus to direct in-contact animals.

Increasing evidence supports the potential of carnivore species, including farmed fur animals, to become infected by SARS-CoV-2.

This transmission could eventually cause zoonotic infections in humans.

Our results indicate that affected farms might be reservoirs for SARS-CoV-2.

Thus, efficient and continuous surveillance should target susceptible animals, including raccoon dogs, especially in China, which is a key player in global fur production.

We also need to initiate large-scale epidemiologic field studies with historical samples that might elucidate the role of farmed animals in the current pandemic.

This article was preprinted. Dr. Freuling is a research scientist at the Friedrich-Loeffler-Institut.

Previously, the World Organisation for Animal Health reported on March 31, 2020, in Hong Kong that neither of the two dogs which were positive for SARS-CoV-2 showed clinical signs of COVID-19 infection.

Mar 22, 2023 • 10:15 am CDT
by Gerd Altmann

Alzamend Neuro, Inc. today announced the completion of the clinical portion of its Phase IIA multiple ascending dose ("MAD") study for dementia related to Alzheimer's.

The topline data is expected to be disclosed in June 2023.

AL001 is a novel lithium-delivery system; it is a lithium-salicylate-L-proline engineered ionic cocrystal under development as an oral treatment for patients with dementia-related to mild, moderate, and severe cognitive impairment associated with Alzheimer's.

AL001 can potentially deliver the benefits of marketed lithium carbonate while mitigating or avoiding current toxicities associated with lithium.

"We strongly believe that AL001's patented ionic cocrystal technology could potentially provide clinicians with a major improvement over current lithium-based treatments and may constitute a means of treating over 40 million American suffering from Alzheimer's, bipolar disorder, MDD, and PTSD," said Stephan Jackman, Chief Executive Officer of Alzamend, in a press release on March 22, 2023.

"We look forward to reporting topline data in June 2023 and further advancing clinical development of this promising potential therapeutic."

Having completed the clinical portion of the MAD study, the resulting pharmacokinetic and statistical data are undergoing evaluation of the safety and tolerability of AL001 under multiple-dose, steady‑state conditions.

This characterizes the maximum tolerated dose in healthy young and elderly subjects and subjects diagnosed with mild to moderate Alzheimer's.

Potentially safe and effective doses will be determined for deployment in planned subsequent Phase IIA clinical trials involving Alzheimer's, bipolar disorder, MDD, and PTSD subjects.

Lithium has been well-characterized for safety and is approved/marketed in multiple formulations for bipolar affective disorders.

AL001 lithium ascending dosing for the MAD cohorts tested incremental fractions of the usual lithium exposure for the treatment of bipolar affective disorder, with the target lithium dose for Alzheimer's treatment expected at a level that will not require therapeutic drug monitoring.

In each of the multiple healthy young/elderly and Alzheimer's cohorts, consisting of 6 active and 2 placebo patients each (as per randomization), multiple ascending doses were administered three times daily for 14 days under fasted conditions up to tolerability/safety limits that included the highest dose permitted per protocol.

As of March 22, 2023, there are no approved vaccines targeting Alzheimer's disease.

Mar 21, 2023 • 2:40 pm CDT
Needle-free Injection System March 2023

PharmaJet® today announced that its partner, Scancell, reported positive results from their Phase 1 COVIDITY clinical trial. The trial was conducted at the University of Cape Town Lung Institute in South Africa to assess the safety and immunogenicity of their COVID-19 DNA candidate vaccines, SCOV1 and SCOV2.

The results from the trial were highly encouraging, inducing neutralizing antibody and T cell responses with no safety concerns. Administration with PharmaJet's devices was well received by study participants.

This new set of human data adds to the growing evidence indicating that this modern needle-free administration technology is an increasingly viable option to enhance plasmid DNA vaccine immune response.

The vaccines were exclusively administered using the PharmaJet Tropis® and Stratis® needle-free precision delivery systems.

Professor Lindy Durrant, Chief Executive Officer, Scancell, commented in a press release on March 21, 2023, "We are encouraged by these results."

"The trial validates that AvidiMab®-modified immunotherapies boost immune responses and PharmaJet's Needle-free Injection Systems are effective in delivering our ImmunoBody®-generated drug candidate."

"Our plans are to include PharmaJet Needle-free precision delivery systems in future trials with our immuno-oncology projects."

PharmaJet Needle-free precision delivery Systems provide increased vaccine effectiveness, a preferred patient and caregiver experience, and a proven path to commercialization.

The Stratis® System has U.S. FDA 510(k) marketing clearance, CE Mark, and WHO PQS certification to deliver medications and vaccines either intramuscularly or subcutaneously.

The Tropis® System has CE Mark and WHO PQS certification for intradermal injections.

They are both commercially available for global immunization programs.

Note: This news article is not paid content.

Mar 21, 2023 • 2:29 pm CDT
by Shane Gaughan

Vaxxinity, Inc. today announced that the first subjects had been dosed in a randomized, double-blind, placebo-controlled Phase 1 clinical trial of VXX-401, an investigational vaccine designed to lower low-density lipoprotein (LDL) cholesterol, a known factor contributing to heart disease.

Heart disease remains the leading cause of death globally, claiming over 18 million deaths yearly.

VXX-401 is designed to induce robust, long-acting antibodies against PCSK9 to lower LDL cholesterol.

The multicenter Phase, 1 dose-escalation trial, aims to enroll 48 subjects aged 18 to 75 years with LDL cholesterol between 2.59 and 4.89 mmol/L.

The trial evaluates safety, tolerability, and immunogenicity (as measured by serum anti-PCSK9 antibody titers).

LDL cholesterol levels will measure the pharmacodynamics of the immune response, an established model of PCSK9 inhibition in hypercholesterolemia. This study was last updated on March 16, 2023.

VXX-401 was designed using Vaxxinity's proprietary synthetic peptide vaccine platform and is being developed to treat hypercholesterolemia.

The platform is designed to harness the immune system to convert the body into its own natural "drug factory," stimulating the production of antibodies.

"This is an exciting milestone for VXX-401 and Vaxxinity in our pursuit to vaccinate the world against heart disease with a preventative option that is convenient and accessible, addressing an unmet need to combat the leading global cause of death," said Mei Mei Hu, Chief Executive Officer of Vaxxinity, in a press release on March 20, 2023.

"PCSK9 antibody therapies are well-tolerated and effective, but huge, unmet patient need remains."

"In order to solve the problem of heart disease, the world needs a scalable, accessible technology that can reach the hundreds of millions, if not billions, of people at risk."

"With an LDL-lowering vaccine, we can offer an option that's cost-effective, safe, convenient, long-acting, and deployable."

Mar 21, 2023 • 12:22 pm CDT
by Muhammad Syafrani

Despite recent improvements in diagnostic tools, chikungunya outbreaks in Africa are probably underreported, stated a U.S. CDC Early Release Dispatch, Volume 29, Number 4—April 2023.

During 2019–2020, a large-scale chikungunya outbreak occurred in Djibouti City, the capital city of the Republic of Djibouti, located in the Horn of Africa.

Djibouti is a semi-arid country bordered by Eritrea, Somalia, and Ethiopia. In this region, the primary vector of the chikungunya virus (CHIKV) is the Aedes aegypti mosquito. 

The chikungunya outbreak remained limited (attack rate 2.1%) but was followed by a dengue outbreak.

These researchers found clinical features helpful but insufficient to discriminate between chikungunya and dengue viruses.

However, CHIKV blood samples on blotting paper have been described as a field method for detecting arboviruses, routinely used in the French Armed Forces when deployed in Africa.

In this study, the researchers used blood samples on blotting paper to detect the emergence of CHIKV and monitor the course of the outbreaks.

Blotting paper provided a robust method for blood sampling and transport to a reference laboratory, making it possible to confirm 90% of the arboviral diagnoses.

We recommend blotting paper as a field tool to detect and monitor arboviral epidemics remotely, wrote these researchers.

Various countries, like Paraguay, are reporting chikungunya outbreaks in remote areas.

As of March 21, 2023, no chikungunya vaccines are authorized in Africa, Europe, or the U.S.

Mar 21, 2023 • 9:37 am CDT
U.S. CDC Norovirus National Trends March 15, 2023

The National Center for Immunization and Respiratory Diseases recently reported data indicating cases of norovirus are spiking in the United States.

Norovirus is a very contagious virus that causes vomiting and diarrhea.

As of March 15, 2023, the 3-week moving average is reaching a new peak since the norovirus outbreak began in August 2022.

Each of the four regions has displayed similar trends, with the Northeast registering the steepest uptick.

In the U.S., cases of norovirus occur most frequently during late fall, winter, and early spring. 

According to the U.S. Centers for Disease Control and Prevention (CDC), people can get norovirus illness many times in their life because there are many different types of noroviruses.

Infection with one type of norovirus may not protect you against other types.

The CDC says it is possible to develop immunity to specific types. But, it is not known exactly how long immunity lasts.

This may explain why so many people of all ages get infected during norovirus outbreaks. About 80% of children will experience a norovirus infection within one year of birth.

As of March 21, 2023, there are no approved norovirus vaccines in the U.S., Europe, or the U.K.

Mar 21, 2023 • 4:40 am CDT
by R. Balouria

The peer review journal The Lancet Infectious Diseases published the results from a recent study examining prospective respiratory syncytial virus (RSV) surveillance data to assess the geotemporal prevalence of RSV A and B and functionally characterize the effect of the nirsevimab binding-site substitutions identified between 2015 and 2021.

Nirsevimab (Beyfortus®), an extended half-life monoclonal antibody (mAbs) to the RSV fusion protein, has been developed to protect infants for an entire RSV season. 

This AstraZeneca and Sanofi-funded observational analysis concluded on March 17, 2023, nirsevimab binding site was highly conserved, and escape variants were rare and have not increased over time.

The U.S. Food and Drug Administration (FDA) initially approved an injectable mAbs therapy for children in 1998.

Beyfortus has been granted various regulatory approvals.

As of March 21, 2023, neither the FDA nor the European Medicines Agency approved an RSV vaccine candidate for children or older adults.

However, various authorizations are expected in 2023.

Mar 21, 2023 • 4:14 am CDT
by Gerd Altmann

Regeneron Pharmaceuticals, Inc. and Sanofi today announced that the European Commission (EC) had approved Dupixent® in the European Union to treat severe atopic dermatitis in children aged six months to 5 years old who are candidates for systemic therapy.

With this approval on March 21, 2023, Dupixent is the first and only targeted medicine indicated to treat these children in Europe and the U.S.

Dupixent is a fully human monoclonal antibody injection administered under the skin at different injection sites.

Atopic dermatitis is a chronic type 2 inflammatory skin disease. Between 85% and 90% of patients first develop symptoms before five years of age, which can often continue through adulthood.

“Watching an infant or young child grapple with the debilitating and wide-reaching impacts of severe atopic dermatitis is heartbreaking,” said Korey Capozza, MPH, Founder and Executive Director of Global Parents for Eczema Research, in a press release.

“I’ve personally witnessed how this chronic skin disease can disrupt the lives of entire families when left uncontrolled. However, intervening with effective treatments during infancy and early childhood can help manage the challenging impact this disease has on children and their families during such formative years.”

Severe atopic dermatitis may also significantly impact the quality of life of young children and their caregivers. Treatment options in this age group are primarily topical corticosteroids, which can be associated with safety risks and may impair growth when used long-term.

The approval is based on data from a Phase 3 trial evaluating Dupixent every four weeks (200 mg or 300 mg based on body weight) plus low-potency primarily topical corticosteroids (TCS) or TCS alone (placebo) in 162 children aged six months to 5 years with moderate-to-severe atopic dermatitis.

At 16 weeks, Dupixent improved skin clearance and reduced overall disease severity and itch compared to placebo in the overall enrolled population. However, in a subset of those with severe atopic dermatitis, patients randomized to Dupixent (n=63) experienced the following compared to placebo (n=62) at 16 weeks:

  • In addition, 46% of patients achieved 75% or greater improvement in overall disease severity compared to 7% treated with placebo, a co-primary endpoint.
  • 14% of patients achieved clear or almost clear skin compared to 2% treated with placebo, a co-primary endpoint.
  • 55% average reduction in overall disease severity from baseline compared to 10% with placebo.
  • 42% average reduction in itch from baseline compared to a 1% increase with placebo.

Dupixent also improved sleep quality, skin pain, and health-related quality of life compared to placebo in both the overall and severe populations. In addition, long-term efficacy data showed the clinical benefit at 16 weeks was sustained through 52 weeks.

The most common side effects across indications include injection site reactions, conjunctivitis, conjunctivitis allergic, arthralgia, oral herpes, and eosinophilia. 

Dupixent is currently approved for one or more indications in more than 60 countries, including Europe, the U.S., and Japan. More than 600,000 patients are being treated with Dupixent globally.