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The U.S. CDC's Morbidity and Mortality Weekly Report published on March 25, 2021, confirmed human papillomavirus (HPV) vaccination is a critical prevention tool against HPV infection, anogenital warts, and HPV-attributable precancers and cancers.

During 2015–2018, the prevalence of 4vHPV types was 88% lower than that during the prevaccine era among females aged 14–19 years and 81% lower among those aged 20–24 years after adjustment for sexual behavior and race/ethnicity.

This CDC report adds to the robust data on the national HPV vaccination program's impact, including herd immunity effects.

In addition to decreases in the prevalence of vaccine types, decreasing rates of cervical precancers and anogenital warts also have been demonstrated in the USA and other countries after the introduction of HPV vaccination.

Unfortunately, the COVID-19 pandemic has the potential to reverse gains made in HPV vaccination coverage, as indicated by lower adolescent vaccine orders in 2020.

The CDC states, 'Efforts are needed to increase HPV vaccination to maintain the vaccination program's substantial progress.'

Furthermore, this new CDC report affirms HPV vaccination is highly effective and is recommended routinely at age 11–12 years and through age 26 years for persons not already vaccinated. Various HPV vaccines are available globally. For more information, please visit this PrecisionVaccinations webpage.

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Takada dengue vaccine TAK-003 is participating in the first-ever parallel assessment of a medicinal product for use in the European Union
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A second Dengue vaccine may soon become available in Europe and elsewhere. Japan-based Takeda Pharmaceutical Company Limited has applied to the European Medicines Agency to Conduct the First-Ever Parallel Assessment of a Medicinal Product for Takeda’s Dengue Vaccine Candidate known as TAK-003.

Additionally, Takada stated in a press release issued on March 25, 2021, besides the EU, it intends to submit Regulatory Filings in Argentina, Brazil, Colombia, Indonesia, Malaysia, Mexico, Singapore, Sri Lanka, Thailand, and the USA during 2021.

If approved, TAK-003 would join Dengvaxia as the only Dengue authorized vaccine.

This news is important since Dengue is the fastest spreading mosquito-borne viral disease. Dengue is mainly spread by Aedes aegypti mosquitoes and, to a lesser extent, Aedes albopictus mosquitoes. It is caused by any of four dengue virus serotypes, each of which can cause dengue fever or severe dengue.

The dengue virus can infect people of all ages and cause serious illness among children in some countries in Latin America and Asia, says the U.S. CDC.

On March 2, 2021, the CDC issued a Level 1 Travel Alert for the Americas, warning international travelers of their risks. Dengue is an ongoing risk in many parts of Central and South America, Mexico, and the Caribbean (map).

“Submission of regulatory filings for our dengue vaccine candidate, TAK-003, marks an important development for people who are living in or traveling to communities burdened by the threat of dengue,” commented Derek Wallace, VP, Dengue Global Program Leader at Takeda.

“Dengue outbreaks, which result in half a million hospitalizations globally each year, can overwhelm communities and governments because of the broad impact on the health care system. With limited options to prevent the disease, there is a pressing need for widely available dengue vaccines. Takeda is committed to working with regulatory authorities and recommending bodies to support evaluation of our submissions and achieve access for TAK-003.” 

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Texas-based Southwest Airlines Co. recently announced it had donated 7,500 roundtrip tickets to help remove the financial burden for those who need to travel for life-changing or specialized medical care.

More than 75 nonprofit hospitals and medical transportation organizations across the United States received the tickets through Southwest's® Medical Transportation Grant Program, allowing them to bring patients and caregivers closer to much-needed medical care.

IN 2021, Southwest is supporting hospitals in 26 states, providing access for patients and their caregivers.

"As the airline with Heart, we have a passion for making a meaningful difference in the communities we serve," commented Laura Nieto, Director of Community Outreach, in a press statement. 

"Through our Medical Transportation Grant Program, we hope to ease the financial burden of air travel expenses and provide a critical lifeline for patients and caregivers, allowing them to stay focused on medical treatment and recovery."

As of March 16, 2021, Southwest began offering passengers a choice of soft drinks during the in-flight drink service. It's the first service enhancement that Southwest has made in nearly a year on its flights.

In its 50th year of service, Dallas-based Southwest Airlines Co. continues to differentiate itself from other air carriers with exemplary Customer Service delivered by more than 56,000 Employees to a Customer base that topped 130 million Passengers in 2019.

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New Jersey-based Seqirus USA Inc. announced the publication of new real-world evidence (RWE) on the company's cell-based quadrivalent seasonal influenza vaccine (QIVc) in the journal Vaccines. 

This retrospective cohort analysis indicated QIVc was more effective in reducing hospitalizations/emergency room (ER) visits caused by influenza, respiratory-related hospitalizations/ER visits, and all-cause hospitalizations compared with an egg-based quadrivalent influenza vaccine (QIVe) among individuals 4–64 years of age during the 2018 - 2019 U.S. flu season.

In an economic analysis, the study also found that QIVc was associated with significantly lower annualized all-cause total costs (($461 savings); p < 0.05) per vaccinated subject, compared with QIVe.

"RWE studies of influenza vaccines provide critical evidence for understanding the impact of annual immunization linked to the circulating viruses in the community," said Stephen I. Pelton, MD, Professor of Pediatrics at Boston University School of Medicine and Public Health & Boston Medical Center, and study author, in a related press statement issued on March 25, 2021.

"Current studies demonstrate that QIVc provides significantly higher effectiveness, compared with standard-dose egg-based quadrivalent influenza vaccine, in preventing all-cause hospitalizations and hospitalizations/ER visits related to any respiratory events including pneumonia and asthma/COPD/bronchial events."

"Also evident is the potential costs saving from QIVc resulting from its greater comparative effectiveness."

This study, published in Vaccines, adds to recent research, including a study published in Clinical Infectious Diseases, demonstrating that QIVc prevented significantly more influenza-related medical encounters among individuals 4 years and older than QIVe during the 2018/19 U.S. influenza season. 

This growing body of evidence indicates that cell-based vaccines like QIVc may potentially result in better influenza-related outcomes compared to standard vaccine options, said Seqirus.

Seqirus is part of CSL Limited and is a major contributor to the prevention of influenza globally and a transcontinental partner in pandemic preparedness with state-of-the-art production facilities in the USA, the U.K., and Australia.

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New York-based Pfizer Inc. announced today real-world evidence (RWE) demonstrating that first-line therapy with IBRANCE® (palbociclib) in combination with letrozole was associated with improved real-world progression-free survival (rwPFS) and overall survival (OS) in women with hormone receptor-positive (HR+), human epidermal growth factor 2-negative (HER2-) metastatic breast cancer (mBC) compared with letrozole alone.

This analysis showed the two-year OS rate was 78.3% in the IBRANCE group and 68.0% with letrozole. The rwPFS and OS benefits were generally consistent across all subgroups, including younger patients (18-50 years of age) and site or extent of metastases.

IBRANCE is an oral inhibitor of CDKs 4 and 6, which are key regulators of the cell cycle that trigger cellular progression.

These findings represent the first comprehensive comparative effectiveness analysis of survival outcomes for a CDK 4/6 inhibitor in routine clinical practice and were published online in Breast Cancer Research.

Chris Boshoff, M.D., Ph.D., Chief Development Officer, Oncology, Pfizer Global Product Development, stated in a press release, “With more than six years of patient experience, a positive benefit-risk profile, strong clinical data, and robust real-world data, the totality of evidence solidifies the role of IBRANCE plus endocrine therapy as a treatment for patients with HR+, HER2- metastatic breast cancer.”

Since the U.S. Food and Drug Administration's initial approval more than six years ago, IBRANCE has been prescribed to more than 380,000 patients across more than 100 countries.

Pfizer Oncology is committed to advancing medicines wherever we believe we can make a meaningful difference in the lives of people living with cancer. Today, we have an industry-leading portfolio of 24 approved innovative cancer medicines and biosimilars across more than 30 indications, including breast, genitourinary, colorectal, blood, and lung cancers, as well as melanoma.

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Caitlin Shockey, a spokesperson for the US Centers for Disease Control and Prevention (CDC), told USA TODAY on March 24, 2021, 'that the Conditional Sailing Order remains in effect.'

"Returning to passenger cruising is a phased approach to mitigate the risk of spreading COVID-19," Shockey said. "Details for the next phase of the CSO are currently under interagency review."

On February 2, 2021, the CDC stated it 'recommends that all people avoid travel on cruise ships, including river cruises, worldwide. That’s because the chance of getting COVID-19 on cruise ships is high since the virus appears to spread more easily between people in close quarters aboard ships.'

Furthermore, the CDC recommends that travelers avoid cruise travel worldwide.

If you travel on a cruise ship or river cruise and disembark in a foreign port, you might not be able to receive appropriate medical care or be medically evacuated if you get sick. Some countries might refuse to dock your ship or allow passengers to disembark. If they identify a case of COVID-19 aboard your cruise ship, foreign health officials may implement formal quarantine procedures, says the CDC.

All air passengers coming to the USA, including U.S. citizens, must have a negative COVID-19 test or documentation of recovery before arriving in the USA.

See the Frequently Asked Questions for more information.

 

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Researchers at the University of Washington School of Medicine and the National Institute of Allergy and Infectious Diseases announced they had developed experimental flu shots that protect animals from a wide variety of seasonal and pandemic influenza strains.

Published in the journal Nature on March 24, 2021, this study details how next-generation flu vaccines may replace current seasonal options by protecting against many more strains that current vaccines do not adequately cover.

The team attached hemagglutinin proteins from four different influenza viruses to custom-made protein nanoparticles to create improved influenza vaccines. This approach enabled an unprecedented level of control over the molecular configuration of the resulting vaccine and yielded an improved immune response compared to conventional flu shots.

"Most flu shots available today are quadrivalent, meaning they are made from four different flu strains. Each year, the World Health Organization makes a bet on which four strains will be most prevalent, but those predictions can be more or less accurate. This is why we often end up with 'mismatched' flu shots that are still helpful but only partially effective," said lead author Daniel Ellis, a research scientist at the Institute for Protein Design at UW Medicine.

"The responses that our vaccine gives against strain-matched viruses are really strong, and the additional coverage we saw against mismatched strains could lower the risk of a bad flu season," said Ellis.

This experimental vaccine is currently being advanced toward several years of human clinical testing and is not available.

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Thermo Fisher Scientific Inc. announced the launch of the AerosolSense Sampler, a new surveillance solution designed to deliver fast and highly reliable insight into the presence of in-air pathogens, including SARS-CoV-2.

Confirming the presence of pathogens like SARS-CoV-2 in a space during a known time interval enables decision-makers in hospitals and other indoor facilities to take actions to protect their employees and provide the public with confidence.

The AerosolSense Sampler is an in-air pathogen surveillance solution that collects representative aerosol samples of ambient air and traps in-air pathogens on a substrate collection substrate. The sample can be readily analyzed through subsequent laboratory testing using polymerase chain reaction (PCR) methodology.

"Such factors as emerging variants, semi-vaccinated populations and varying levels of compliance with COVID-19 personal safety protocols, continue to pose risks to a society looking to return to life as it was before the pandemic," commented Mark Stevenson, EVP, and COO of Thermo Fisher Scientific, in a press statement.

"It is important that easy-to-use, highly reliable solutions be available to allow hospitals, nursing homes, schools, businesses, and government institutions to identify the presence of in-air pathogens quickly so that safety protocols can be put into action, validated, or strengthened."

Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $30 billion. 

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Rabies Vaccines

Rabies Vaccines 2025

Rabies is a vaccine-preventable viral disease found in more than 150 countries and territories, according to the World Health Organization (WHO). Two types of vaccines protect people against Rabies: nerve tissue and cell culture vaccines. Cell culture vaccines, which are more affordable and require less vaccine, have been developed recently. Unlike conventional, inactivated rabies vaccines, live-attenuated viruses are genetically modified viruses that can replicate in a vaccinated person without causing adverse effects while eliciting robust and effective immune responses against viral infection.

As of 2025, according to the WHO, intradermal immunization using cell-culture-based rabies vaccines is an acceptable alternative to standard intramuscular administration. In the United Kingdom, rabies vaccines must be inactivated or recombinant and approved for use in the country. 

Rabies Vaccines Approved

As of 2025, the WHO has pre-qualified rabies vaccines, including Bavarian Nordic's RabAvert vaccIVAX-S by Serum Institute of India Pvt. Ltd., VaxiRab N by Zydus Lifesciences Limited, and VERORAB by Sanofi Pasteur.

RabAvert is a vaccine that contains an inactivated rabies antigen, indicated for preexposure vaccination, primary and booster doses, and post-exposure prophylaxis against Rabies in all age groups.

Chirorab®, previously known as Rabipur, is an inactivated rabies virus of Flury LEP. Chiron Behring Vaccines is relaunching Rabipur, a purified chick-embryo-celline. It will continue manufacturing at its WHO-prequalified facility in Ankleshwar, Gujarat, India.

Rabipur is an inactivated rabies vaccine produced by Valneva SE, which has over 35 years of worldwide clinical experience.

Rabivax-S is a lyophilized vaccine manufactured by Serum Institute of India Pvt. Ltd. It contains inactivated, purified rabies antigen and was developed using Vero cells (ATCC CCL81), derived from the Pitman-Moore strain. The inactivated vaccine is freeze-dried until ready for immunization.

Rabies Vaccine Candidates

Rabies vaccine candidates are seeking participants for various clinical trials in 2025. 

YS Biopharma Co., Ltd. PIKA Rabies Vaccine utilizes the company's proprietary PIKA adjuvant technology, designed to produce a more robust immune response in a shorter timeframe than traditional rabies vaccines. On April 9, 2024, YS Bio announced positive interim results from the ongoing Phase 3 clinical trial, indicating that the PIKA Rabies Vaccine has successfully met the primary endpoints and has the potential to achieve best-in-class accelerated protection and meet the WHO's goal of a one-week rabies vaccine regimen to replace the conventional three- or four-week regimens. On June 1, 2023, the Food and Drug Administration of the Philippines approved a Phase 3 clinical trial, and on May 16, 2023, Pakistan issued study approval.

Replicate Bioscience announced on September 12, 2023, the dosing of the first participant in a Phase 1 trial of its RBI-4000 vaccine candidate for rabies prevention. The Trial marks the first time a human has been dosed with Replicate's next-generation srRNA technology, which will be a benchmark for its utility in this indication.

VitriVax, Inc. received a grant of up to $5 million from the Coalition for Epidemic Preparedness Innovations to develop further Atomic Layering Thermostable Antigen and Adjuvant (ALTA) technology, using Rabies as a vaccine target. ALTA® could replace multi-dose vaccines for protection against infectious diseases with a single-administration alternative.

Rabies Vaccine Preexposure Prophylaxis (PrEP)

The WHO recommends preexposure prophylaxis (PrEP) for individuals at high risk of exposure. The WHO position paper on rabies vaccines recommends a one-week, two-site intradermal post-exposure prophylaxis (PEP) schedule with 0.1 mL of vaccine injected on days 0, 3, and 7. The U.S. Centers for Disease Control and Prevention (CDC) updated its recommendations for rRabies post-exposure prophylaxis (PrEP) for humans, replacing the three-dose vaccination schedule with a two-dose program intended to protect people for at least three years. On May 6, 2022, the U.S. CDC published Use of a Modified Preexposure Prophylaxis Vaccination Schedule to Prevent Human Rabies: Recommendations of the Advisory Committee on Immunization Practices — United States, 2022. 

Rabies Vaccine Breakthrough Infections

A case report by Holzbauer et al. in the March 2023 issue of Clinical Infectious Diseases is not a situation of inappropriate prophylaxis; rather, it represents a textbook response to accurate exposure to Rabies. An 84-year-old awoke to a bat biting his finger. The man washed his finger with soap and water, as recommended. Post-exposure prophylaxis was initiated three days after exposure. He received a complete four-vaccine regimen and more than the recommended 20 IU/kg of human rabies immunoglobulin (the actual dose was reportedly 30.9 IU/kg, as determined by potency testing of the immunoglobulin used), partially injected into the bite site, with the remaining amount given intramuscularly. Yet, five months later, he developed clinical Rabies and succumbed to it.

Importation of Dogs Without Rabies

In the U.S., stray dog control programs were initiated in the 1940s, and routine rabies vaccination of owned dogs eliminated the canine rabies virus variant from circulation by 2008. The American Animal Hospital Association Canine Vaccination Guidelines were updated in 2022. As of August 2023, a valid CDC Rabies Vaccination and Microchip Record is needed to obtain a permit or make a reservation. The CDC does not accept foreign-issued pet passports or other certificates for rabies vaccinations administered outside the United States. Rabies-vaccinated dogs vaccinated in the U.S. by a U.S.-licensed veterinarian may re-enter the country from a high-risk country without a CDC Dog Import Permit if the dog has a current, valid U.S.-issued rabies vaccination certificate and an ISO-compatible microchip. The CDC has temporarily suspended the importation of dogs from high-risk countries with Rabies until July 31, 2024.

Rabies Vaccines Raccoons

The U.S. Department of Agriculture's Animal and Plant Health Inspection Service announced on August 4, 2023, that it will begin its annual distribution of RABORAL V-RG®, an oral rabies vaccine bait, in select areas in the eastern United States to prevent the spread of raccoon rabies. Raccoons, foxes (including red and gray varieties), skunks, and bats are considered primary carriers of the rabies virus in the United States.

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Rabies vaccines are approved and offered worldwide in 2025
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