- Vaccine doses allocated to 9 African countries hardest hit by mpox surgeThe Access and Allocation Mechanism (AAM) for mpox has allocated an initial 899 000 vaccine doses for 9 countries across the African region that are hit hard by the current mpox surge. In collaboration with affected countries and donors, this decision aims to ensure that the limited doses are used effectively and fairly, with the overall objective to control the outbreaks. The AAM principals from the Africa Centres for Disease Control and Prevention (Africa CDC), the Coalition for Epidemic Preparedness Innovations (CEPI), Gavi, the Vaccine Alliance (Gavi), UNICEF, and the World Health Organization (WHO) approved the allocation, following the recommendations of an independent Technical Review Committee of the Continental Incident Management Support Team for mpox. The decision was informed by country readiness and epidemiological data. The 9 countries are the Central African Republic, Cote d’Ivoire, the Democratic Republic of the Congo, Kenya, Liberia, Nigeria, Rwanda, South Africa and Uganda. The largest number of doses – 85% of the allocation – will go to the Democratic Republic of the Congo as the most affected country, reporting four out of every five laboratory-confirmed cases in Africa this year. These doses come from Canada, Gavi, the Vaccine Alliance, the European Union (Austria, Belgium, Croatia, Cyprus, France, Germany, Luxemburg, Malta, Netherlands, Poland, Portugal and Spain, as well as the European Union Health Emergency Response Authority), and the United States of America. The outbreak of mpox, particularly the surge of the viral strain clade Ib, in the Democratic Republic of the Congo and neighbouring countries was declared a public health emergency of international concern by WHO and a public health emergency of continental security by Africa CDC in mid-August. This year, 19 countries in Africa have reported mpox, many of them newly affected by the viral disease. The epicentre of the outbreak remains the Democratic Republic of the Congo, with over 38 000 suspected cases and over 1000 deaths reported this year. Vaccination is recommended as a part of a comprehensive mpox response strategy, focusing also on timely testing and diagnosis, effective clinical care, infection prevention, and the engagement of affected communities. Vaccines play an important role and are recommended to reduce transmission and help contain outbreaks. In recent weeks, limited vaccination has begun in the Democratic Republic of the Congo and Rwanda. This allocation to the 9 countries marks a significant step towards a coordinated and targeted deployment of vaccines to stop the mpox outbreaks. For most countries, the rollout of mpox vaccines will be a new undertaking. Implementing targeted vaccination requires additional resources. Partners of the mpox AAM, set up last month, are working to scale up the response. Further allocations of vaccines are expected before the end of the year. Notes to editors Key points of the vaccination approach under the global and continental strategic preparedness and response plans: Vaccine availability: Over 5.85 million vaccine doses are expected to be available to the Mpox Vaccines AAM by the end of 2024, including the nearly 900 000 allocated doses. The supply includes contributions from multiple nations and organizations, including 1.85 million dose donations of MVA-BN from the European Union, United States, and Canada, 500 000 doses of MVA-BN from Gavi utilizing the First Response Fund, 500 000 doses procured through UNICEF, as well as a further 3 million doses of the LC16 vaccine from Japan. Phased vaccination strategy: • Phase 1: Stop outbreaks – Focused on interrupting transmission through targeted vaccination of people at highest risk of infection including contacts of confirmed cases, health-care workers, frontline responders, and key at-risk populations in areas with active human to human transmission. • Phase 2: Expand protection – To protect more people at risk in affected communities, as additional doses of vaccine are available. It targets individuals at high risk of severe disease – based on local epidemiology – in affected areas, focusing on regions with the highest incidence of mpox. Special attention will be given to vulnerable populations, including those living with HIV, internally displaced persons, and refugees, due to their increased risk of severe outcomes. • Phase 3: Protect for the future – Aimed at building population immunity to guard against future outbreaks as part of a longer-term mpox control programme. The first phase targets the vaccination of approximately 1.4 million people at risk of infection by the end of 2024, with an initial 2.8 million doses of the MVA-BN vaccine to be allocated for this effort. Maximizing the impact of vaccines through strategic vaccination is crucial: Implementing targeted vaccination approaches can reduce transmission by focusing on those at the highest risk of infection. This vaccination strategy prioritizes individuals at substantially higher risk of exposure, including close contacts – such as household members and sexual partners – of confirmed cases. A combination of prevention and control interventions are recommended to optimize the effectiveness of vaccination efforts. Demand planning for Phase 2: Current demand forecasts for Phase 2 estimate the need to vaccinate at least an additional 10 million individuals to protect high-risk groups across Africa. The projection is based on current epidemiological data and emerging information on transmission patterns. These estimates will be updated as more data becomes available, and the outbreak trajectory evolves. Regulatory and policy updates: The WHO Strategic Advisory Group of Experts (SAGE) recommends off-label use of vaccines for children and pregnant women in outbreak settings. Urgent action is required to expedite regulatory pathways for vaccine approval across affected countries, ensuring timely access for infants and children. Additionally, delivery support must be strengthened to address in-country vaccine delivery challenges and ensure efficient distribution.
- WHO study lists top endemic pathogens for which new vaccines are urgently neededA new World Health Organization (WHO) study published today in eBioMedicine names 17 pathogens that regularly cause diseases in communities as top priorities for new vaccine development. The WHO study is the first global effort to systematically prioritize endemic pathogens based on criteria that included regional disease burden, antimicrobial resistance risk and socioeconomic impact. The study reconfirms longstanding priorities for vaccine research and development (R&D), including for HIV, malaria, and tuberculosis – three diseases that collectively take nearly 2.5 million lives each year. The study also identifies pathogens such as Group A streptococcus and Klebsiella pneumoniae as top disease control priorities in all regions, highlighting the urgency to develop new vaccines for pathogens increasingly resistant to antimicrobials. “Too often global decisions on new vaccines have been solely driven by return on investment, rather than by the number of lives that could be saved in the most vulnerable communities,” said Dr Kate O’Brien, Director of the Immunization, Vaccines and Biologicals Department at WHO. “This study uses broad regional expertise and data to assess vaccines that would not only significantly reduce diseases that greatly impact communities today but also reduce the medical costs that families and health systems face.” WHO asked international and regional experts to identify factors that are most important to them when deciding which vaccines to introduce and use. The analysis of those preferences, combined with regional data for each pathogen, resulted in top 10 priority pathogens for each WHO region. The regional lists where then consolidated to form the global list, resulting in 17 priority endemic pathogens for which new vaccines need to be researched, developed and used. This new WHO global priority list of endemic pathogens for vaccine R&D supports the Immunization Agenda 2030’s goal of ensuring that everyone, in all regions, can benefit from vaccines that protect them from serious diseases. The list provides an equitable and transparent evidence base to set regional and global agendas for new vaccine R&D and manufacturing, and is intended to give academics, funders, manufacturers and countries a clear direction for where vaccine R&D could have the most impact. This global prioritization exercise for endemic pathogens, complements the WHO R&D blueprint for epidemics, which identified priority pathogens that could cause future epidemics or pandemics, such as COVID-19 or severe acute respiratory syndrome (SARS). The findings of this new report on endemic pathogens are part of WHO’s work to identify and support the research priorities and needs of immunization programmes in low- and middle-income countries, to inform the global vaccine R&D agenda, and to strategically advance development and uptake of priority vaccines, particularly against pathogens that cause the largest public health burden and greatest socioeconomic impact. WHO Priority endemic pathogens list Vaccines for these pathogens are at different stages of development. Pathogens where vaccine research is needed Group A streptococcus Hepatitis C virus HIV-1 Klebsiella pneumoniae Pathogens where vaccines need to be further developed Cytomegalovirus Influenza virus (broadly protective vaccine) Leishmania species Non-typhoidal Salmonella Norovirus Plasmodium falciparum (malaria) Shigella species Staphylococcus aureus Pathogens where vaccines are approaching regulatory approval, policy recommendation or introduction Dengue virus Group B streptococcus Extra-intestinal pathogenic E. coli Mycobacterium tuberculosis Respiratory syncytial virus (RSV)
- Vaccine doses allocated to 9 African countries hardest hit by mpox surgeThe Access and Allocation Mechanism (AAM) for mpox has allocated an initial 899 000 vaccine doses for 9 countries across the African region that are hit hard by the current mpox surge. In collaboration with affected countries and donors, this decision aims to ensure that the limited doses are used effectively and fairly, with the overall objective to control the outbreaks. The AAM principals from the Africa Centres for Disease Control and Prevention (Africa CDC), the Coalition for Epidemic Preparedness Innovations (CEPI), Gavi, the Vaccine Alliance (Gavi), UNICEF, and the World Health Organization (WHO) approved the allocation, following the recommendations of an independent Technical Review Committee of the Continental Incident Management Support Team for mpox. The decision was informed by country readiness and epidemiological data. The 9 countries are the Central African Republic, Cote d’Ivoire, the Democratic Republic of the Congo, Kenya, Liberia, Nigeria, Rwanda, South Africa and Uganda. The largest number of doses – 85% of the allocation – will go to the Democratic Republic of the Congo as the most affected country, reporting four out of every five laboratory-confirmed cases in Africa this year. These doses come from Canada, Gavi, the Vaccine Alliance, the European Union (Austria, Belgium, Croatia, Cyprus, France, Germany, Luxemburg, Malta, Netherlands, Poland, Portugal and Spain, as well as the European Union Health Emergency Response Authority), and the United States of America. The outbreak of mpox, particularly the surge of the viral strain clade Ib, in the Democratic Republic of the Congo and neighbouring countries was declared a public health emergency of international concern by WHO and a public health emergency of continental security by Africa CDC in mid-August. This year, 19 countries in Africa have reported mpox, many of them newly affected by the viral disease. The epicentre of the outbreak remains the Democratic Republic of the Congo, with over 38 000 suspected cases and over 1000 deaths reported this year. Vaccination is recommended as a part of a comprehensive mpox response strategy, focusing also on timely testing and diagnosis, effective clinical care, infection prevention, and the engagement of affected communities. Vaccines play an important role and are recommended to reduce transmission and help contain outbreaks. In recent weeks, limited vaccination has begun in the Democratic Republic of the Congo and Rwanda. This allocation to the 9 countries marks a significant step towards a coordinated and targeted deployment of vaccines to stop the mpox outbreaks. For most countries, the rollout of mpox vaccines will be a new undertaking. Implementing targeted vaccination requires additional resources. Partners of the mpox AAM, set up last month, are working to scale up the response. Further allocations of vaccines are expected before the end of the year. Notes to editors Key points of the vaccination approach under the global and continental strategic preparedness and response plans: Vaccine availability: Over 5.85 million vaccine doses are expected to be available to the Mpox Vaccines AAM by the end of 2024, including the nearly 900 000 allocated doses. The supply includes contributions from multiple nations and organizations, including 1.85 million dose donations of MVA-BN from the European Union, United States, and Canada, 500 000 doses of MVA-BN from Gavi utilizing the First Response Fund, 500 000 doses procured through UNICEF, as well as a further 3 million doses of the LC16 vaccine from Japan. Phased vaccination strategy: • Phase 1: Stop outbreaks – Focused on interrupting transmission through targeted vaccination of people at highest risk of infection including contacts of confirmed cases, health-care workers, frontline responders, and key at-risk populations in areas with active human to human transmission. • Phase 2: Expand protection – To protect more people at risk in affected communities, as additional doses of vaccine are available. It targets individuals at high risk of severe disease – based on local epidemiology – in affected areas, focusing on regions with the highest incidence of mpox. Special attention will be given to vulnerable populations, including those living with HIV, internally displaced persons, and refugees, due to their increased risk of severe outcomes. • Phase 3: Protect for the future – Aimed at building population immunity to guard against future outbreaks as part of a longer-term mpox control programme. The first phase targets the vaccination of approximately 1.4 million people at risk of infection by the end of 2024, with an initial 2.8 million doses of the MVA-BN vaccine to be allocated for this effort. Maximizing the impact of vaccines through strategic vaccination is crucial: Implementing targeted vaccination approaches can reduce transmission by focusing on those at the highest risk of infection. This vaccination strategy prioritizes individuals at substantially higher risk of exposure, including close contacts – such as household members and sexual partners – of confirmed cases. A combination of prevention and control interventions are recommended to optimize the effectiveness of vaccination efforts. Demand planning for Phase 2: Current demand forecasts for Phase 2 estimate the need to vaccinate at least an additional 10 million individuals to protect high-risk groups across Africa. The projection is based on current epidemiological data and emerging information on transmission patterns. These estimates will be updated as more data becomes available, and the outbreak trajectory evolves. Regulatory and policy updates: The WHO Strategic Advisory Group of Experts (SAGE) recommends off-label use of vaccines for children and pregnant women in outbreak settings. Urgent action is required to expedite regulatory pathways for vaccine approval across affected countries, ensuring timely access for infants and children. Additionally, delivery support must be strengthened to address in-country vaccine delivery challenges and ensure efficient distribution.
- WHO study lists top endemic pathogens for which new vaccines are urgently neededA new World Health Organization (WHO) study published today in eBioMedicine names 17 pathogens that regularly cause diseases in communities as top priorities for new vaccine development. The WHO study is the first global effort to systematically prioritize endemic pathogens based on criteria that included regional disease burden, antimicrobial resistance risk and socioeconomic impact. The study reconfirms longstanding priorities for vaccine research and development (R&D), including for HIV, malaria, and tuberculosis – three diseases that collectively take nearly 2.5 million lives each year. The study also identifies pathogens such as Group A streptococcus and Klebsiella pneumoniae as top disease control priorities in all regions, highlighting the urgency to develop new vaccines for pathogens increasingly resistant to antimicrobials. “Too often global decisions on new vaccines have been solely driven by return on investment, rather than by the number of lives that could be saved in the most vulnerable communities,” said Dr Kate O’Brien, Director of the Immunization, Vaccines and Biologicals Department at WHO. “This study uses broad regional expertise and data to assess vaccines that would not only significantly reduce diseases that greatly impact communities today but also reduce the medical costs that families and health systems face.” WHO asked international and regional experts to identify factors that are most important to them when deciding which vaccines to introduce and use. The analysis of those preferences, combined with regional data for each pathogen, resulted in top 10 priority pathogens for each WHO region. The regional lists where then consolidated to form the global list, resulting in 17 priority endemic pathogens for which new vaccines need to be researched, developed and used. This new WHO global priority list of endemic pathogens for vaccine R&D supports the Immunization Agenda 2030’s goal of ensuring that everyone, in all regions, can benefit from vaccines that protect them from serious diseases. The list provides an equitable and transparent evidence base to set regional and global agendas for new vaccine R&D and manufacturing, and is intended to give academics, funders, manufacturers and countries a clear direction for where vaccine R&D could have the most impact. This global prioritization exercise for endemic pathogens, complements the WHO R&D blueprint for epidemics, which identified priority pathogens that could cause future epidemics or pandemics, such as COVID-19 or severe acute respiratory syndrome (SARS). The findings of this new report on endemic pathogens are part of WHO’s work to identify and support the research priorities and needs of immunization programmes in low- and middle-income countries, to inform the global vaccine R&D agenda, and to strategically advance development and uptake of priority vaccines, particularly against pathogens that cause the largest public health burden and greatest socioeconomic impact. WHO Priority endemic pathogens list Vaccines for these pathogens are at different stages of development. Pathogens where vaccine research is needed Group A streptococcus Hepatitis C virus HIV-1 Klebsiella pneumoniae Pathogens where vaccines need to be further developed Cytomegalovirus Influenza virus (broadly protective vaccine) Leishmania species Non-typhoidal Salmonella Norovirus Plasmodium falciparum (malaria) Shigella species Staphylococcus aureus Pathogens where vaccines are approaching regulatory approval, policy recommendation or introduction Dengue virus Group B streptococcus Extra-intestinal pathogenic E. coli Mycobacterium tuberculosis Respiratory syncytial virus (RSV)
- Statement by Principals of the Inter-Agency Standing Committee – Stop the assault on Palestinians in Gaza and on those trying to help themWe the leaders of 15 United Nations and humanitarian organizations urge, yet again, all parties fighting in Gaza to protect civilians, and call on the State of Israel to cease its assault on Gaza and on the humanitarians trying to help. The situation unfolding in North Gaza is apocalyptic. The area has been under siege for almost a month, denied basic aid and life-saving supplies while bombardment and other attacks continue. Just in the past few days, hundreds of Palestinians have been killed, most of them women and children, and thousands have once again been forcibly displaced. Hospitals have been almost entirely cut off from supplies and have come under attack, killing patients, destroying vital equipment, and disrupting life-saving services. Health workers and patients have been taken into custody. Fighting has also reportedly taken place inside hospitals. Dozens of schools serving as shelters have been bombed or forcibly evacuated. Tents sheltering displaced families have been shelled, and people have been burned alive. Rescue teams have been deliberately attacked and thwarted in their attempts to pull people buried under the rubble of their homes. The needs of women and girls are overwhelming and growing every day. We have lost contact with those we support and those who provide lifesaving essential services for sexual and reproductive health and gender-based violence. And we have received reports of civilians being targeted while trying to seek safety, and of men and boys being arrested and taken to unknown locations for detention. Livestock are also dying, crop lands have been destroyed, trees burned to the ground, and agrifood systems infrastructure has been decimated. The entire Palestinian population in North Gaza is at imminent risk of dying from disease, famine and violence. Humanitarian aid cannot keep up with the scale of the needs due to the access constraints. Basic, life-saving goods are not available. Humanitarians are not safe to do their work and are blocked by Israeli forces and by insecurity from reaching people in need. In a further blow to the humanitarian response, the polio vaccination campaign has been delayed due to the fighting, putting the lives of children in the region at risk. And this week, the Israeli Parliament adopted legislation that would ban UNRWA and revoke its privileges and immunities. If implemented, such measures would be a catastrophe for the humanitarian response in Gaza, diametrically opposed to the United Nations Charter, with potential dire impacts on the human rights of the millions of Palestinians depending on UNRWA’s assistance, and in violation of Israel’s obligations under international law. Let us be very clear: There is no alternative to UNRWA. The blatant disregard for basic humanity and for the laws of war must stop. International humanitarian law, including the rules of distinction, proportionality and precautions, must be respected. IHL obligations do not depend on reciprocity. No violation by one party ever releases the other from its legal obligations. Attacks against civilians and what remains of civilian infrastructure in Gaza must stop. Humanitarian relief must be facilitated, and we urge all parties to provide unimpeded access to affected people. Additionally, commercial goods must be allowed to enter Gaza. The wounded and sick must receive the care they need. Medical personnel and hospitals must be spared. Hospitals should not turn into battlegrounds. Unlawfully detained Palestinians must be released. Israel must comply with the provisional orders and determinations of the International Court of Justice. Hamas and other Palestinian armed groups must release the hostages immediately and unconditionally and must abide by international humanitarian law. Member States must use their leverage to ensure respect for international law. This includes withholding arms transfers where there is a clear risk that such arms will be used in violation of international law. The entire region is on the edge of a precipice. An immediate cessation of hostilities and a sustained, unconditional ceasefire are long overdue. Signatories: Ms. Joyce Msuya, Acting Emergency Relief Coordinator and Under-Secretary-General for Humanitarian Affairs (OCHA) Ms. Nimo Hassan, MBE, Chair, International Council of Voluntary Agencies (ICVA) Mr. Jamie Munn, Executive Director, International Council of Voluntary Agencies (ICVA) Ms. Amy E. Pope, Director General, International Organization for Migration (IOM) Mr. Volker Türk, United Nations High Commissioner for Human Rights (OHCHR) Ms. Abby Maxman, President and Chief Executive Officer, Oxfam Ms. Paula Gaviria Betancur, United Nations Special Rapporteur on the Human Rights of Internally Displaced Persons (SR on HR of IDPs) Mr. Achim Steiner, Administrator, United Nations Development Programme (UNDP) Ms. Anacláudia Rossbach, Executive Director, United Nations Human Settlement Programme (UN-Habitat) Mr. Filippo Grandi, United Nations High Commissioner for Refugees (UNHCR) Dr. Natalia Kanem, Executive Director, United Nations Population Fund (UNFPA) Ms. Catherine Russell, Executive Director, UN Children's Fund (UNICEF) Ms. Sima Bahous, Under-Secretary-General and Executive Director, UN Women Ms. Cindy McCain, Executive Director, World Food Programme (WFP) Dr. Tedros Adhanom Ghebreyesus, Director-General, World Health Organization (WHO)
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