Vaccine News

Vaccine news brought to you by Precision Vaccinations.

Jan 29, 2024 • 4:54 pm CST
US CDC Yellow Book 2024

According to the U.S. CDC Yellow Book 2024, an international traveler's risk for acquiring Yellow Fever virus is determined by their immunization status and destination-specific and travel-associated factors. 

Since about thirty countries require proof of a pre-arrival yellow fever vaccination, many travelers have questions about the vaccine's long-term efficacy.

On January 22, 2024, the Lancet Global Health recently published results from a systematic review aimed at assessing the necessity of a booster vaccination based on the long-term (10+ years) immunogenicity of primary yellow fever vaccination in travelers and in residents of yellow fever-endemic areas, as well as in specific populations, including children and immunocompromised individuals.

The gathered evidence suggested that a single dose of yellow fever vaccine provides lifelong protection (overall seroprotection rate 94%) in travelers.

However, in people living with HIV and young children (<2 years), booster doses might still be required because lower proportions of vaccinees were seroprotected ten or more years post-vaccination.

The pooled seroprotection rate was 47% in children and 61% in people living with HIV. 

Lower observed seroprotection rates among residents of yellow fever endemic areas were partly explained by the use of a higher cutoff for seroprotection that was applied in Brazil. No conclusions could be drawn for the sub-Saharan Africa region.

The CDC says most people infected with yellow fever do not get sick or have only mild symptoms. People who get sick will start having symptoms 3–6 days after infection.

According to the CDC, about 12% of people with symptoms develop serious illnesses.

The study was registered with PROSPERO, CRD42023384087. No industry conflicts of interest were disclosed.

Jan 29, 2024 • 4:26 pm CST
US CDC flu shots 2024

The journal Clinical Microbiology and Infection published the results from a post-hoc analysis regarding the relative effectiveness of high-dose quadrivalent influenza vaccine (QIV-HD) vs. standard-dose quadrivalent influenza vaccine (QIV-SD) against recurrent hospitalizations for seniors.

Published on January 27, 2024, this analysis found that among 12,477 randomly assigned participants, receiving QIV-HD was associated with lower incidence rates of hospitalisations for pneumonia or influenza (10 vs. 33 events, IRR 0.30 [95% CI 0.14-0.64], p=0.002).

And all-cause hospitalisations (647 vs. 742 events, IRR 0.87 [95% CI 0.76-0.99], p=0.032) compared with QIV-SD.

These researchers wrote, 'Our exploratory results correspond to a number needed to treat 65 (95% CI 35-840) persons vaccinated with QIV-HD compared with QIV-SD to prevent one additional all-cause hospitalization per season.'

'Further research is needed to confirm these hypothesis-generating findings.'

As of January 29, 2024, over 156 million cell, egg, and nasal-based influenza vaccines were distributed in the U.S. during the 2023-2024 flu season.

Jan 29, 2024 • 9:24 am CST
from Pixabay

Anyone can get pneumococcal disease, but some people are at increased risk. To better protect children and seniors from disease, innovative vaccine candidates are conducting clinical trials in 2024.

Currently, two kinds of pneumococcal vaccines are recommended in the U.S. - Pneumococcal conjugate vaccines (PCVs, specifically PCV15 and PCV20) and Pneumococcal polysaccharide vaccine (PPSV23).

However, even with U.S. FDA-approved vaccines broadly available, approximately 5,000 deaths are related to pneumococcal disease each year in the U.S.

To address this health issue, Vaxcyte, Inc. today announced the completion of enrollment in its Phase 1/2 clinical study evaluating VAX-31, a next-generation 31-valent PCV and the broadest-spectrum pneumococcal vaccine candidate in the clinic today. 

This vaccine candidate is designed to prevent invasive pneumococcal disease (IPD).

Vaxcyte expects to announce topline safety, tolerability, and immunogenicity data from the Phase 1/2 study in the third quarter of 2024.

"Completing the enrollment of the VAX-31 study with more than one thousand adults 50 years and older is a significant step for our PCV franchise, and we look forward to announcing topline safety, tolerability, and immunogenicity data in the third quarter of this year," said Grant Pickering, Chief Executive Officer and Co-founder of Vaxcyte, in a press release.

"VAX-31, the broadest-spectrum PCV in the clinic, has the potential to address a significant public health need by covering approximately 95% of IPD circulating in the U.S. adult population while maintaining coverage of previously circulating strains that are currently contained via ongoing vaccination."

Vaxcyte's unedited press release is posted here.

Jan 28, 2024 • 11:38 am CST
Taiwan CDC vaccinations 2024

In September 2023, the Taiwan Centers for Disease Control (Taiwan CDC) announced that mRNA vaccines would continue to be available in response to the continued spread of COVID-19.

However, according to Novavax Inc.'s announcement on January 23, 2024, the updated protein-based non-mRNA COVID-19 vaccine (Nuvaxovid™XBB.1.5 dispersion for injection) is now available for use in Taiwan for the prevention of COVID-19 in individuals aged 12 and older.

Doses have been distributed by Taiwan CDC to local vaccination clinics across the country.

The Taiwan CDC stated that adding a protein-based vaccine will diversify the country's vaccine portfolio and provide a non-mRNA option to help protect against COVID-19.

"We are working closely with Taiwan's authorities to ensure doses of our updated protein-based non-mRNA COVID-19 vaccine are made available at vaccination centers across Taiwan as soon as possible," said John C. Jacobs, President and Chief Executive Officer, Novavax, in a press release posted on December 18, 2023.

Throughout the multi-year pandemic, about 90% of Taiwan's population contracted COVID-19, and 19,005 people died.

Taiwan's authorization was based on non-clinical data showing that Novavax's updated COVID-19 vaccine induced functional immune responses for XBB.1.5, XBB.1.16, and XBB.2.3 variants.

Additional non-clinical data demonstrated that Novavax's NVX-CoV2601 vaccine-induced neutralizing antibody responses to subvariants BA.2.86, EG.5.1, FL.1.5.1, and XBB.1.16.6 as well as CD4+ polyfunctional cellular (T-cell) responses against EG.5.1 and XBB.1.16.6.

These data indicate Novavax's vaccine can stimulate both arms of the immune system and induce a broad response against circulating variants, says Novavax.

Jan 27, 2024 • 3:01 pm CST
by Kone Kassoum

Malaria affects millions of lives annually, particularly in tropical and subtropical regions, according to a Perspective published by the Malaria Journal.

Despite being largely preventable, malaria outbreaks caused  247 million infections and over 600,000 deaths across 85 countries in 2021,

In the ongoing battle against malaria outbreaks, a promising development has emerged with the endorsement by the World Health Organization of the R21/Matrix-M™ Malaria Vaccine.

Developed through a collaboration between the University of Oxford and Novavax Inc., this vaccine has demonstrated remarkable efficacy, reaching 77% effectiveness in Phase 2 clinical trials.

R21 is designed to be low-dose, cost-effective, and accessible, with approval for use in children under three years old.

Published on January 12, 2024, this paper critically examines the R21/Matrix-M malaria vaccine, its development, potential impact on global malaria eradication efforts, and the challenges and opportunities it presents.

The U.S. Centers for Disease Control and Prevention says about 2,000 malaria cases are diagnosed in the United States annually, mostly in travelers returning to cities such as Miami, Florida.

As of January 27, 2024, malaria vaccines are unavailable in the U.S.

Jan 27, 2024 • 11:07 am CST
US CDC typhoid case map 2023

A recent study funded by the Bill & Melinda Gates Foundation found that a single-dose vaccine against typhoid was efficacious for at least four years among children in all age groups.

The Vi polysaccharide conjugated to tetanus toxoid vaccine's vaccine efficacies by age group were 70·6% (6·4–93·0) for children aged nine months to 2 years; 79·6% (45·8–93·9) for children aged 2–4 years; and 79·3% (63·5–89·0) for children aged 5–12 years.

These phase 3 clinical trial results, published by The Lancet on January 25, 2024, support current World Health Organization (WHO) recommendations in typhoid-endemic areas for mass campaigns among children aged nine months to 15 years, followed by routine introduction in the first two years of life.

An estimated 11–21 million cases of typhoid fever and 5 million cases of paratyphoid fever occur worldwide each year, causing an estimated 135,000–230,000 deaths. The CDC says there are very few typhoid cases in the United States each year.

Jan 27, 2024 • 10:13 am CST
US CDC FluView data January 26, 2024

According to new data posted by the U.S. Centers for Disease Control and Prevention (CDC), ten additional children died from influenza last week.

Six deaths were associated with influenza A viruses, such as A(H1N1).

Three deaths were associated with influenza B viruses with no lineage determined.

One pediatric death was associated with a co-infection with influenza A(H1N1) and influenza B/Victoria viruses.

As of January 26, 2024, the CDC's FluView dashboard indicates a total of 57 influenza-associated pediatric deaths have now occurred during the 2023-2024 flu season.

During the 2022-2023 flu season, 183 children died from influenza infections. The CDC has not indicated the vaccination status of the fatalities.

From an overall impact perspective, the National Center for Health Statistics reported from October 2, 2022, to September 9, 2023, of all deaths in the U.S., 9,697 (4%) of death certificates listed influenza.

While the CDC stated last Friday that key flu indicators have decreased or remained stable nationally for three weeks, there is an ample supply of flu shots (egg, cell, and nasal-based) offered at most pharmacies in the U.S. 

Over 156 million flu vaccines had been distributed during the 2023-2024 season. This decreased from the 173 million influenza vaccines distributed last flu season.

Jan 26, 2024 • 12:55 pm CST
by Jason Goh

The journal Nature Biotechnology volume recently confirmed that Japanese regulators are proceeding to launch a second-generation COVID-19 vaccine that uses self-amplifying messenger RNA (sa-mRNA), the first vaccine of this kind to get full approval.

According to the News in Brief article posted on January 17, 2024, the innovative sa-mRNA ARCT-154 vaccine enables host cells in the body to make copies of the mRNA that encodes viral replicase genes and immunogenic genes. 

Co-developed by Arcturus Therapeutics and CSL, ARCT-154 uses a lower concentration than conventional mRNA vaccines to achieve similar or better antigen expression, meaning they could be safer and manufactured on a large scale.

The vaccine's approval by Japan's Ministry of Health was announced in November 2023.

Japan has administered 434,119,370 COVID-19 vaccine doses throughout the pandemic as of January 16, 2024.

Arcturus and CSL have also filed an MAA for European regulatory approval of ARCT-154.

Jan 26, 2024 • 11:50 am CST
by Pixabay

The U.S. Centers for Disease Control and Prevention (CDC) today published a COCA Now email alert confirming that in most of the continental United States, the ABRYSVO™ respiratory syncytial virus (RSV) vaccine should be given to pregnant women from September through January 31, regardless of year-to-year circulation, when infants would be born during increased RSV activity,

As of late January 2024, numerous indicators show RSV infection decreasing in the U.S. 

Jurisdictions that have different RSV seasonality from most of the continental United States, such as Alaska, southern Florida, Guam, Hawaii, Puerto Rico, the U.S.-affiliated Pacific Islands, and the U.S. Virgin Islands, may consider RSV vaccination of pregnant women after January 31.

The CDC and its Advisory Committee on Immunization Practices recommend the RSV vaccination during 32–36 weeks gestation.

The CDC recently reported among women who were pregnant and ≥32 weeks gestation since September 22, 2023, the overall coverage with the RSV vaccine was 14.4% as of January 13, 2024.

Infants born to unvaccinated mothers should receive Beyfortus™ (nirsevimab). This single-dose, long-acting monoclonal antibody provides immediate, passive immunity protection to the infant against RSV-associated lower respiratory tract disease.

As of 2024, Beyfortus availability has increased in the U.S.

COCA Now emails will be sent as soon as possible after the CDC publishes new content, ensuring clinicians are updated.

Jan 25, 2024 • 5:06 pm CST
by Katharina

A recent population-based observational study conducted in Scotland highlights the positive impact of human papillomavirus (HPV) vaccination in young women and the benefits of early vaccination.

Published by the Journal of the National Cancer Institute on January 22, 2024, this study reported no cases of invasive cervical cancer were recorded in women immunized at 12 or 13 years of age, irrespective of the number of doses.

Women vaccinated between 14 to 22 years of age and given three doses of the bivalent HPV vaccine showed a significant reduction in incidence compared with all unvaccinated women (3.2/100 000 [95% confidence interval (CI) = 2.1 to 4.6] vs 8.4 [95% CI = 7.2 to 9.6]).

Data for women born between January 1988 and June 5, 1996, were extracted from the Scottish cervical cancer screening system in July 2020 and linked to cancer registry, immunization, and deprivation data.

According to the U.S. CDC, HPV is the most common sexually transmitted infection in the U.S. People get HPV by having vaginal, anal, or oral sex with someone who has the virus. A study in the U.S. recently discovered that within two years of a new relationship, about 40% of unvaccinated women contract HPV.

As of January 25, 2024, 140 countries have introduced an HPV vaccine into immunization programs.

There are various approved HPV vaccines and numerous vaccine candidates conducting clinical research.

Jan 25, 2024 • 1:23 pm CST
US CDC measles case trends 2023

According to a Clinician Outreach and Communication Activity COCA Now message published today, the U.S. Centers for Disease Control and Prevention (CDC) was notified of 23 measles cases between December 2023 and January 23, 2024.

On January 24, 2024, this COCA Now email stated these cases include seven direct importations of measles by international travelers and two outbreaks with more than five cases each. 

Specifically, most of the recent measles cases were among children and adolescents who had not received a measles-containing vaccine, even if they were age-eligible.

The increased number of measles importations in the U.S. reflects a rise in global measles outbreaks

Over the past year, the CDC says Yemen (23,066) and India (13,997) have reported the most measles cases.

In the U.S., the Philadelphia Department of Public Health recently reported a measles cluster among unvaccinated residents. Nine measles cases have been confirmed in Philadelphia locations in 2024.

The Georgia Department of Public Health confirmed a measles case in an unvaccinated Atlanta resident.

The Virginia Department of Health was notified of a confirmed case of measles in a person who traveled through Northern Virginia airports.

In greater Kansas City, Missouri, a resident at the Kansas City International Airport and North Kansas City Hospital was infected with the measles virus.

And in Washington, six measles cases were confirmed in January 2024.

In the U.S., various measles vaccines, such as GSK's Priorix, are generally available at local pharmacies.

COCA Now emails will be sent as soon as possible after the CDC publishes new content, ensuring clinicians are updated.

Jan 25, 2024 • 5:03 am CST
by Gerd Altmann

Novavax, Inc. today announced that the United Kingdom's (U.K.) Medicines and Healthcare products Regulatory Agency (MHRA) granted marketing authorization for Nuvaxovid XBB.1.5 dispersion for injection, COVID-19 Vaccine (recombinant, adjuvanted) for active immunization to prevent COVID-19 in individuals aged 12 and older.

Recent data indicate Novavax's vaccine can stimulate both arms of the immune system and induce a broad response against circulating variants.

"Today's MHRA authorization is recognition of the role our vaccine can have in protecting the British public against COVID-19 this year," said John C. Jacobs, President and Chief Executive Officer, Novavax, in a press release on January 24, 2024.

"We are in ongoing conversations with additional U.K. partners to identify potential opportunities to offer our protein-based non-mRNA COVID-19 vaccine to all eligible individuals who want one."

"We believe this is critical to supporting long-term, broad uptake of a seasonal COVID-19 vaccine in the U.K."

In clinical trials, the most common adverse reactions associated with Novavax's prototype COVID-19 vaccine (NVX-CoV2373) included headache, nausea or vomiting, muscle pain, joint pain, injection site tenderness, injection site pain, fatigue, and malaise.

If people are concerned about an adverse event, it should be reported on a Yellow Card. Reporting forms and information can be found at https://coronavirus-yellowcard.mhra.gov.uk/.

The U.K. authorization was based on non-clinical data showing that Novavax's updated COVID-19 vaccine induced functional immune responses for XBB.1.5, XBB.1.16, and XBB.2.3 variants.

Additional non-clinical data demonstrated that Novavax's vaccine-induced neutralizing antibody responses to subvariants JN.1, BA.2.86, EG.5.1, FL.1.5.1, and XBB.1.16.6, as well as CD4+ polyfunctional cellular (T-cell) responses against EG.5.1 and XBB.1.16.6.

In 2023, the U.S. Food and Drug Administration amended its authorization for Novavax COVID-19 Vaccine, Adjuvanted for use in individuals 12 and older, to include the 2023-2024 formula. 

Novavax COVID-19 vaccine brands include Nuvaxovid, NVX-CoV2601, CovoVax, NVX-CoV2373, and TAK-019, Trademark filing #90813423.

Jan 24, 2024 • 12:51 pm CST
US CDC COVIDVaxView data Jan. 23, 2024

According to the U.S. Centers for Disease Control and Prevention (CDC) COVIDVaxView data, about 11% (CI 10.1 to 11.8) of children under the age of 18 are up to date with their COVID-19 vaccinations.

From a state perspective, as of January 23, 2024, Massachusetts has reached about a third of children with COVID-19 vaccinations.

Furthermore, Louisana was the lowest-ranked state, with only 3.1% (CI 1.2 to 5.0) of children up to date.

The CDC says up to date with the updated 2023-24 COVID-19 vaccine is defined as receipt of at least one vaccination since September 14, 2023, for children ≥5 years; for children <5 years, up-to-date status was defined based on the current recommendations that also take into account number of doses and brand of vaccine.

Up-to-date status was determined by survey questions on the month and year of the most recent COVID vaccine, and for children <5 years, the total number of COVID vaccinations received and brand of the most recent COVID vaccine.

Each week, estimates for prior weeks are recalculated by the CDC using the additional interviews conducted that week.

Jan 24, 2024 • 9:39 am CST
WHO malaria vaccine shipments 2024

The Ministry of Health of the Republic of Liberia today announced the arrival of 112,000 doses of the Mosquirix™ (RTS,S) malaria vaccine.

GSK's Mosquirix vaccine has been piloted in Africa since 2019 and has been shown to be safe and effective, reducing severe malaria by 30% and malaria deaths by 13%.

With two malaria vaccines now approved for use in Africa, Liberia's fight against this preventable mosquito-borne disease may save thousands of children's lives. Malaria vaccinations are scheduled to launch in April 2024.

"The arrival of this life-saving vaccine is a game changer in our fight against malaria," said Adolphus Clarke, Director of the Expanded Programme on Immunization at the Ministry of Health of Liberia, in a press release on January 23, 2024.

"We are committed to ensuring that every child in Liberia has access to this vaccine and is protected from this deadly disease."

According to the World Health Organization, eleven countries saw an estimated 249 million malaria cases and 426,000 deaths in 2022.

In the United States, about ten locally acquired malaria cases were reported in 2023.

However, malaria vaccines are not available in the U.S. as of January 2024.

Jan 24, 2024 • 5:19 am CST
CEPI 2024

The Coalition for Epidemic Preparedness Innovations (CEPI) today announced Serum Institute of India Pvt. Ltd (SII) has joined CEPI's network of vaccine producers in the Global South to support more rapid, agile, and equitable responses to future public health disease outbreaks.

To prepare for such a scenario, CEPI is investing up to $30 million to build upon SII's proven track record of rapid response to infectious disease outbreaks, expanding the company's ability to swiftly supply investigational vaccines in the face of epidemic and pandemic threats.

Created by CEPI to expand the global footprint of vaccine production, the manufacturing network focuses on vaccine makers in the Global South near areas at high risk of outbreaks caused by deadly viral threats like Lassa Fever, Nipah, Disease X, and other pathogens with epidemic or pandemic potential prioritized by CEPI.

Dr. Richard Hatchett, CEO of CEPI, said in a press release on January 23, 2024, "As part of CEPI's global manufacturing network, SII's world-renowned manufacturing and rapid response capabilities are poised to play a critical role in enabling swift and equitable access to affordable outbreak vaccines for the Global South."

Given SII's already proven production capabilities, the company may be called upon to promptly supply investigational vaccines for preclinical and clinical testing and large-scale supply in the event of an outbreak.

Shortening the time taken to manufacture and validate the first batches of experimental vaccines will be vital to enabling a response to an escalating outbreak within just 100 days – a goal created by CEPI and embraced by the G7, G20, and industry leaders – and could help stop a future pandemic in its tracks.