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The U.S. Centers for Disease Control and Prevention (CDC) today announced Advisory Committee on Immunization Practices (ACIP) recommended updates to the 2023 childhood and adult immunization schedules.

These enhancements were voted on by the ACIP committee on October 20, 2022, including incorporating additional information for approved or authorized COVID-19 vaccines.

The CDC wrote in a media statement, 'It has been almost two years since COVID-19 vaccines were first rolled out in the U.S., and nearly 630 million doses have since been administered nationwide.'

'It's important to note that there are no changes in COVID-19 vaccine policy, and today's action simply helps streamline clinical guidance for healthcare providers by including all currently licensed, authorized, and routinely recommended vaccines in one document.'

The 'ACIP's recommendation to add COVID-19 vaccines to the routinely recommended vaccine schedule represents another step in the nation's recovery.'

The updated vaccination schedules and program clinical guidance will be published in early 2023. 

The CDC will continue to update and work with health departments, providers, and other partners over the coming months to ensure a smooth transition of the COVID-19 vaccination program from emergency response to a routine immunization program activity.

Note: The U.S. CDC recommends using vaccines, while state or local jurisdictions determine school entry and other vaccination requirements.

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Ebola Outbreaks

Ebola Outbreaks April 2025

The initial Zaire Ebolavirus disease case was confirmed in 1976 in a village near the Ebola River in Africa, according to the World Health Organization (WHO). A study published on August 18, 2023, says the origins of Ebola remain enigmatic. Recent data suggest that some Ebola virus (EBOV) outbreaks may originate from the human-to-human transmission of prior Ebola virus disease (EBVD) outbreak strains, rather than spillover. Orthoebolaviruses are a group of four viruses that cause Ebola disease. As of April 26, 2025, more than 30 EBVD outbreaks have been reported. The WHO posted a Chronology of EBOV outbreaks.

Zaire Ebolavirus Outbreaks

Africa experienced Ebola virus outbreaks in the Democratic Republic of the Congo (DRC), formerly known as Zaire, in 2014, 2016, 2018, and 2022. Over 29,000 people were infected, and more than 11,000 died. The African countries most afflicted were Sierra Leone and Liberia. Since then, the Democratic Republic of the Congo (DRC) Ministry of Health has announced various outbreaks of EVD. During the 2018 Ebola virus disease (EVD) outbreak in the eastern Democratic Republic of the Congo (DRC), among those offered vaccination, self-reported uptake of the Ebola vaccine was 99% (95% confidence interval [CI] 98.0–99.4%). As of August 2023, Original Research indicates that EVD surveillance systems in Liberia may fail to detect a new outbreak promptly. According to the WHO, specific improvements are required, and regular evaluations are recommended. The U.S. government conducted airport screenings for the Zaire Ebola virus in 2014.

Sudan Ebolavirus Outbreak

The Uganda Ministry of Health declared its eighth Sudan Ebolavirus Disease (SVD) outbreak in January 2025. As of April 26, 2025, Uganda's second SVD outbreak in three years was declared over by the WHO Africa. During this SVD outbreak, 14 cases and four deaths occurred.

The U.S. CDC reissued a Travel Health Advisory Level 2, Practice Enhanced Precautions notice on March 12, 2025, regarding Uganda's current SVD outbreak. The CDC previously issued Health Alert Network Health Advisory CDCHAN-00477 on October 6, 2022, and CDCHAN-00480 on November 7, 2022. Since October 2022, all U.S.-bound passengers from Uganda have been routed to designated airports for enhanced Ebola screening. Traveler screening at Ugandan entry points remains active in 2025, with 25,364 travelers screened for SVD as of March 2, 2025.

The UKHSA issued a public health message in November 2022 regarding the SVD outbreak in Uganda. All workers returning to the UK from areas affected by SUDV should undergo a risk assessment. On November 1, 2022, the WHO advised against imposing any travel and/or trade restrictions on Uganda based on the available information regarding the current SUDV outbreak.

On May 8, 2023, North Kivu, DRC, confirmed a positive case of SUDV.

Ebola in the United States

The U.S. CDC updated its Ebola Outbreak History on August 31, 2023. The CDC says that 11 people were treated for EVD in the U.S. during Africa's 2014-2016 epidemic. On September 30, 2014, the CDC confirmed the first travel-associated case of Zaire EVD was diagnosed in the U.S. in a traveler from West Africa to Dallas, Texas. The patient (the index case) died on October 8, 2014. Two healthcare workers who cared for him tested positive for EVD, and both recovered. On October 23, 2014, a medical aid worker who had volunteered in Guinea was hospitalized in New York City, NY, and was diagnosed with EVD. The aid worker recovered, and seven others were cared for in West Africa. Six of these EVD patients recovered; one died, reported the CDC.

Ebola Vaccines

As of April 2025, Ebola vaccines are not commercially available in the United States. Ebola vaccine information is posted at the Vax-Before-Travel link.

Ebola Therapy

The U.S. Food and Drug Administration authorized Ebanga for intravenous injections on December 21, 2020.

Ebola Prevention and Control Guidelines

In August 2024, the WHO published updated research priorities for infection prevention and control in healthcare settings. Key recommendations are summarized in The BMJ. On December 18, 2023, Texas Biomed announced findings published in the Journal of Infectious Diseases (Sept. 2023) indicating that the Ebola virus creates and uses intercellular tunnels to move from cell to cell and evade treatments. "Our findings suggest that the virus can create its hiding place, hide, and then move to new cells and replicate," says Olena Shtanko, Ph.D., an Assistant Professor at Texas Biomed and senior author.

Ebolavirus Diagnostic Tests

A novel patch-based ebolavirus diagnostic test was announced in August 2023.

Ebolavirus Disease

The Ebolavirus family Filoviridae includes three genera: Cuevavirus, Marburgvirus, and Ebolavirus. Within the genus Ebolavirus, six species have been identified: Sudan, Zaire, Bundibugyo, Reston, Taï Forest, and Bombali. Ebola viruses (EBOV) assemble into filamentous virions whose shape and stability are determined by the matrix viral protein 40 (VP40). The pH-driven structural remodeling of the VP40 matrix acts as a molecular switch coupling viral matrix uncoating to membrane fusion during EBOV entry. According to the WHO, EVD is transmitted to people from wild animals and spread through human-to-human transmission, with case fatality rates varying from 25% to 90%. The time from infection with the Ebola virus to symptom onset, including fever, fatigue, muscle pain, headache, and sore throat, can range from 2 to 21 days.

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Jynneos vaccine is a two dose regimen
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The U.S. CDC's Advisory Committee on Immunization Practices vaccine committee reviewed today a monoclonal antibody (mAbs) for preventing Respiratory Syncytial Virus (RSV) in infants.

The Beyfortus® (Nirsevimab) review is essential since about 2-3% of all infants are hospitalized for RSV.

While most mAbs benefits decrease over time, some evidence suggests that Beyfortus protection extends beyond 150 days, although the degree of this protection is yet to be determined.

An analysis from South Africa showed a hazard ratio of 0.491 (95% CI 0.158, 1.523).

And neutralizing antibody titers were 7x higher than baseline at day 361 in Beyfortus-treated subjects and were significantly higher than those with natural infection.

Generally, vaccines offer a longer protection duration, but current RSV vaccine clinical studies lack extensive data.

The European Medicines Agency Committee for Medicinal Products for Human Use adopted on September 16, 2022, a positive opinion for Beyfortus to prevent RSV lower respiratory tract disease in newborns and infants during their first RSV season.

If approved, Beyfortus would be the first and only single-dose passive immunization for the broad infant population, including those born healthy, at term or preterm, or with specific health conditions.

Additional RSV vaccine and mAbs news are posted at PrecisionVaccination.com/RSV.

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The U.K. Health Security Agency published today the National flu and COVID-19 surveillance report for the 2022 to 2023 season, with data indicating the flu season has started across England.

Through Respiratory Datamart, influenza positivity increased to 4.1% in week #41.

Positivity was highest in the 5 to 14-year-old group at 10.8%, followed by the 15 to 44-year-olds at 8.1%.

Furthermore, the U.K. confirmed on October 20, 2022, it recently launched the new flu shot program and reported the following immunization rates:

  • 18.2% under 65 years in a clinical risk group,
  • 49.5% of 65-year-olds and over,
  • 12.1% in 2-year-olds,
  • 12.8% of 3-year-olds,
  • 12.4% of all pregnant women.

Additionally, the U.K. confirmed other respiratory disease infections during week #41, such as:

  • Respiratory syncytial virus (RSV) positivity increased to 5.7% in week 41, with the highest positivity in the under-5-year-olds at 18.5%,
  • Adenovirus positivity increased to 3.1%,
  • Rhinovirus positivity decreased to 16.9% overall,
  • Parainfluenza positivity remained low at 1.3%,
  • Human metapneumovirus positivity remained low at 0.9%.

Additional 2022-2023 flu season vaccination news is posted at PrecisionVaccinations.com/Flu.

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The International Coordinating Group (ICG) today announced it would temporarily suspend the standard two-dose vaccination regimen in cholera outbreak response campaigns, using a single-dose approach instead.  

The ICG stated on October 19, 2022, the current supply of cholera vaccines is extremely limited. The benefit of supplying one cholera dose still outweighs no doses.

As vaccine manufacturers are producing at their maximum current capacity, there is no short-term solution to increase production.

The ICG's action is related to various cholera outbreaks this year.

Since January 2022, 29 countries have reported cholera cases, including Haiti, Malawi, and Syria, facing large outbreaks.

In comparison, in the previous five years, fewer than 20 countries, on average reported outbreaks.

The one-dose strategy has proven effective in responding to outbreaks, even though evidence on the exact duration of protection is limited, and protection appears to be much lower in children.  

Previous studies indicated a two-dose regimen; when the second dose is administrated within six months of the first, immunity against infection lasts for three years.

The ICG manages the global stockpile of oral cholera vaccines.

Of the total 36 million doses forecast to be produced in 2022, 24 million have already been shipped for preventive (17%), and the ICG approved reactive (83%) campaigns and an additional 8 million doses for the second round for emergency vaccination in four countries.

The ICG will continue to monitor the global epidemiological trends and the status of the cholera vaccine stockpile and will review this decision regularly.

Currently, there are three WHO pre-qualified oral cholera vaccines: Dukoral®, ShanChol™, and Euvichol®, mainly used for international travelers.

Other cholera vaccine news is posted at Vax-Before-Travel.com/Cholera.

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Polio Vaccines

Polio Vaccines August 2025

As of 2025, two types of poliomyelitis vaccines are in use, according to the U.S. Centers for Disease Control and Prevention (CDC), the European Medicines Agency (EMA), the United Kingdom's NHS, and the World Health Organization (WHO). The inactivated (killed) polio vaccine (IPV) was developed by Dr. Jonas Salk in 1955 and has been offered in the U.S. since 2000. IPVs produce antibodies in the blood that target all three types of poliovirus, thereby preventing the virus from spreading. The live attenuated (weakened) oral polio vaccine (OPV) was developed by Dr. Albert Sabin in 1961. 

As of August 14, 2025, the Global Polio Eradication Initiative (GPEI) states that the OPV contains a weakened strain of the poliovirus that has evolved over time and now behaves similarly to wild-type polio infections. In addition, OPV can mutate sufficiently to regain virulence and lead to vaccine-derived poliovirus, which can paralyze an unvaccinated person. OPVs not only eradicated serotype 2, but they also resulted in decreased mortality rates among young children. The OPV confers cross-protection against non-polio enteroviruses, respiratory viruses, and herpes viruses due to the early activation of CD4+ and CD8+ T cells via pattern-recognition receptors, the reconfiguration of innate immune cells through epigenetic manipulation, and cross-reaction between B cells and T cells, among other mechanisms.

World Health Organization Polio Vaccination Recommendations

The WHO's SAGE reiterated in 2024 that timely OPV remains the primary tool for outbreak response because it elicits mucosal immunity. However, it was noted that the immunogenicity of OPV in settings where WPV1 or cVDPV outbreaks occur is often suboptimal. It is recommended that IPV be administered concomitantly with the novel OPV type 2 (nOPV2) during outbreak response vaccination campaigns, unless this would impact the timeliness of the response. In areas with co-circulation of poliovirus types 1 and 2, SAGE recommended concomitant administration of nOPV2 together with IPV. In September 2024, the SAGE expressed support for planning the eventual global cessation of bivalent oral poliovirus vaccines (bOPV) use. The Global OPV Stockpile Strategy for 2022-2026 was published in 2023.

Polio Vaccinations U.S. CDC

The IPV vaccine has been available in the U.S. since 2000. As of August 2025, the CDC says the IPV can reduce the amount of poliovirus people shed, but can't stop all virus transmission. The CDC published a poliovirus vaccine update, recommending that children receive four doses of any combination of IPV and trivalent oral polio vaccine (tOPV) or a primary series of at least three doses of IPV or tOPV. The OPV is not offered in the U.S. Since 1961, the FDA has required testing to ensure that polio vaccines used in the United States are free of SV40 contamination.

Polio Vaccine Effectiveness

Estimates of vaccine effectiveness against paralytic polio range from 36% to 89% for one dose, and IPV vaccination appears to reduce the mean quantity of shed poliovirus by 63% to 91%. Research indicates no significant differences in the odds of poliovirus shedding between individuals with IPV and those who are unvaccinated. A U.S. CDC-funded study published by The Lancet on May 10, 2023, concluded that co-administration of nOPV2 and bOPV interfered with immunogenicity for poliovirus type 2 but not for types 1 and 3. The blunted nOPV2 immunogenicity we observed would be a significant drawback of co-administration as a vaccination strategy.

Polio Vaccine Booster Dose

On December 4, 2023, the U.S. CDC MMWR published updated recommendations for the use of IPV for adults known to be unvaccinated or incompletely vaccinated. States that fully vaccinated adults are at increased risk for poliovirus exposure may receive a single lifetime booster dose of IPV. The CDC's  Advisory Committee on Immunization Practices (ACIP), led by Oliver Brooks, MD, FAAP, reviewed poliovirus, polio vaccination, and polio epidemiology on June 21, 2023. The ACIP's Proposed Language: Adults who have received a primary series of tOPV or IPV in any combination and are at increased risk of poliovirus exposure may receive another (booster) dose of IPV. Available data do not indicate the need for more than one lifetime booster dose for adults with IPV. Sarah Kidd, MD, MPH, led the ACIP presentation on Adult Polio Vaccination: Recommendations for Unvaccinated and Incompletely Vaccinated Adults, as well as Recommendations for Booster Doses of IPV.

Polio Vaccines 2025

IMARC Group's new report indicates that the poliomyelitis vaccine market is expected to exhibit a CAGR of 5.04% from 2024 to 2034.

PT Bio Farma and Biological E. Limited produce the WHO-prequalified nOPV2 vaccine. As of July 2024, approximately one billion doses have been administered in more than 35 countries worldwide.

The Imovax Polio® (IPOL® IPV) vaccine is indicated for active immunization of infants (as young as six weeks), children, and adults to prevent poliomyelitis caused by poliovirus types 1, 2, and 3. The IPV protects against both wild-type polio and this weakened poliovirus strain. On February 28, 2024, the CDC vaccine committee reviewed the Clinical Considerations for Children Who Received a Fractional Dose of Inactivated Poliovaccine. Refer to the ACIP IPV catch-up vaccine table for details and age groups.

Kinrix is indicated as the fifth dose in the IPV series for active immunization against diphtheria, tetanus, pertussis, and poliomyelitis in children ages 4 through 6.

Pediarix is a vaccine for active immunization against diphtheria, tetanus, pertussis, hepatitis B, and infection caused by all known subtypes of the hepatitis B virus, as well as poliomyelitis. 

Pentacel is a multi-vaccine that contains diphtheria, tetanus toxoids, and acellular pertussis adsorbed, as well as inactivated poliovirus (DTaP-IPV), which is common, as well as an ActHIBHIB vaccine component.

Quadracel vaccine is indicated for active immunization against diphtheria, tetanus, pertussis, and poliomyelitis.

SanShantha Biotechnics manufactures Sanofi's IMOVAX-Polio IPV vaccine in Hyderabad and has been used in over 100 countries for more than 40 years. ShanIPV IPV is an inactivated polio vaccine developed by Shantha Biotechnics. It received WHO prequalification status and was produced by Sanofi in Hyderabad, India, until December 2023Sanofi Pasteur became the first contributor to IPV in India in March 2014.

Sabin IPV, an inactivated vaccine produced by SINOVAC Biotech Ltd., is indicated for preventing the wild poliovirus and was WHO-prequalified in June 2022.

LGChem (Eupolio) is the first attenuated Sabin-IPV to obtain WHO prequalification. The main advantage is a lower biosafety risk.

SINOVAC's sIPV polio vaccine was WHO-prequalified in June 2022 to prevent poliomyelitis caused by infection with types I, II, and III polioviruses. sIPV is available for purchase by United Nations agencies.

Bio Farma bOPV Bivalent Type 1 & 3 Oral Poliomyelitis Vaccine.

Bilthoven Biologicals produces an inactivated polio vaccine and plans to collaborate with Bharat Bio to develop an OPVtech.

Codagenix Inc. received funding to apply its proprietary synthetic biology technology to fortify nOPV strains against recombination with other enteroviruses, thereby further reducing the risk of emergence of potentially neurovirulent vaccine-derived polioviruses.

Novel Oral Polio Vaccine

Bio Farma manufactures novel OPV candidates against polio types 1 and 3, and they are undergoing several clinical studies sponsored by PATH. Since the nOPV2 vaccine launched in Africa, approximately 1 billion doses have been administered in more than 29 countries. The U.S. CDC confirmed the nOPV2 vaccine is more genetically stable and less likely to be associated with the emergence of cVDPV2.

A study published in The Lancet Infectious Diseases on August 13, 2025, showed results of a phase 1 randomized controlled trial show that the novel live attenuated type 1 and 3 oral polio vaccines (nOPV1 and nOPV3) have a favorable safety profile and produce a comparable immune response and viral-shedding profile as the homotypic monovalent (single-strain) Sabin-strain oral vaccines (mOPVs).

Polio Vaccination United Kingdom

The UK Health Security Agency (UKHSA) confirmed that an IPV Booster campaign was launched in London on September 29, 2022,  targeting children aged 1 in 2022. The polio vaccine is part of the NHS childhood vaccination schedule.

Polio Vaccine Fractional Dose

In 2016, the World Health Organization (WHO) announced a global shortage of IPV, specifically in India. In response, WHO's Strategic Advisory Group of Experts on Immunization (SAGE) recommended a strategic shift to fractional-dose inactivated poliovirus vaccine (fIPV), a smaller dose of the same vaccine equivalent to 1/5 of a standard dose, according to the GPEI. Studies show that two doses of fractional-dose IPV administered by intradermal injection produce a more robust immune response than a single full-dose IPV dose.

Polio Vaccine Price

The U.S. CDC confirms that the Vaccines For Children program is a federally funded program that provides IPV vaccines and medicines at no cost to children who might not otherwise be vaccinated due to their inability to pay. The U.S. CDC Vaccine Price List was updated in 2023. This UNICEF table provides an overview. For people in the U.S. who are not covered by health insurance, a polio booster typically costs around $100. For example, pharmacies may charge about $100 for an IPV polio booster shot. 

Polio Vaccine Misinformation Management

Yale Institute for Global Health and The Public Good Projects partnered in 2020 to create the Vaccine Misinformation Management Field Guide. This guide aims to help organizations address the global infodemic by developing strategic and well-coordinated national action plans to rapidly counter vaccine misinformation and build demand for vaccinations informed by social listening. The Digital Community Engagement (DCE) initiative recruits digital volunteers through an interactive online platform, uInfluence, to promote accurate information on polio and vaccines. In 2022, over 5 million online social listening results were analyzed from 41 countries in more than 100 languages. 

Polio Vaccine Transition

In 2016, the CDC announced that to address the risks posed by type 2 circulating vaccine-derived polioviruses, the type 2 component of the OPV was withdrawn through a switch from the tOPV to the bOPV, which contains only attenuated viruses of types 1 and 3. However, the bOPV vaccine does not offer immunity against serotype 2. This change reduced the risk of tOPV seeding new cVDPV2 outbreaks in the U.S. 

The GPEI reports that, before April 2016, the trivalent oral poliovirus vaccine (tOPV), which contains types 1, 2, and 3, was the predominant vaccine used for routine immunization against poliovirus. Before the development of tOPV, monovalent OPVs (mOPV2) were developed in the early 1950s but were discontinued upon the adoption of tOPV. Following April 2016, the tOPV was replaced with the bivalent oral poliovirus vaccine (bOPV). As of February 2023, the tOPV remains used with children in countries such as Somalia. On August 9, 2023, the Strategy Committee of the GPEI announced that it had commissioned a formal evaluation of the 2016 global withdrawal of Sabin poliovirus type 2 (OPV2), the switch from tOPV to bOPV. The review aims to generate critical lessons learned from the OPV2 withdrawal to guide the direction of the GPEI, including future OPV withdrawal efforts. The finalization and publication of the evaluation are planned for mid-2024. On May 12, 2023, the CDC reported that from January to 021 March 31, 2023, GPEI supported 48 countries, during which approximately 988 million bOPV, 616,000 IPV, 960,000 fractional IPV, 90 million mOPV2, 595 million nOPV2, and 100 million tOPV doses were administered. The 6th Transition Independent Monitoring Board report was published on August 2, 2023, evaluating the progress and challenges of the polio transition process and recommending strengthening work at the global, regional, and country levels. 

Poliovirus Outbreaks

The latest news on polio outbreaks is posted by Vax-Before-Travel in 2025.

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Novavax COVID-19 Vaccine authorized as a booster for adults
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GSK plc recently announced that the U.S. Food and Drug Administration (FDA) had approved a new presentation of Menveo [Meningococcal Oligosaccharide Diptheria CRM197 Conjugate Vaccine for individuals aged 10 to 55 years to help prevent invasive meningococcal disease caused by Neisseria meningitidis serogroups A, C, Y, and W.

The Menveo one-vial presentation will initially be available to U.S. federal customers, with broader availability anticipated in mid-2023.

The original two-vial presentation of Menveo requiring reconstitution was approved by the FDA in 2010 and remains available for use in individuals from two months to 55 years of age.

The Menveo vaccine for meningococcal groups A, C, Y, and W has been approved in over 60 countries, with more than 72 million doses distributed worldwide since 2010.

Roger Connor, President, Vaccines and Global Health, GSK, said in a press release on October 17, 2022, "Outbreaks of this dangerous disease continue to occur, impacting families, health systems, and society."

The U.S. CDC says the meningococcal disease is rare and has declined in the U.S. since the 1990s. However, anyone can get meningococcal disease. 

It can cause meningitis (infection of the lining of the brain and spinal cord) and blood infections.

Even when treated, meningococcal disease has a fatality rate of about 15% of infected people.

And of those who survive, disabilities such as hearing loss, brain damage, kidney damage, loss of limbs, nervous system problems, or severe scars from skin grafts are prevalent.

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