Teresa Aguado
World Health Organization
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Publication
Featured researches published by Teresa Aguado.
The Lancet | 2003
Luis Jódar; F. Marc LaForce; Costante Ceccarini; Teresa Aguado; Dan M. Granoff
Preferred profile of a vaccine for prevention of epidemic meningococcal disease in sub-Saharan Africa: Confers durable protective immunity after one dose. Interrupts transmission of the organism in the population thereby indirectly protecting unimmunised people from disease (herd immunity). Safe and manufactured in compliance with European Pharmacopoeia and WHO standards—ultimate acceptance of the vaccination program in Africa depends on high standards for quality control production and rigorous licensure process. Available in the shortest timeframe possible without compromising effectiveness or safety. Production of 25 million doses per year for 10 years. Price low enough to facilitate widespread use in Africa (estimated
Vaccine | 2012
Mamoudou H. Djingarey; Rodrigue Barry; Mete Bonkoungou; Sylvestre Tiendrebeogo; Rene Sebgo; Denis Kandolo; Clément Lingani; Marie-Pierre Preziosi; Patrick Zuber; William Perea; Stéphane Hugonnet; Nora Dellepiane de Rey Tolve; Carole Tevi-Benissan; Thomas A. Clark; Leonard W. Mayer; Ryan T. Novak; Nancy E. Messonier; Monique Berlier; Desire Toboe; Deo Nshimirimana; Richard Mihigo; Teresa Aguado; Fabien Diomandé; Paul A. Kristiansen; Dominique A. Caugant; F. Marc LaForce
A new Group A meningococcal (Men A) conjugate vaccine, MenAfriVac™, was prequalified by the World Health Organization (WHO) in June 2010. Because Burkina Faso has repeatedly suffered meningitis epidemics due to Group A Neisseria meningitidis special efforts were made to conduct a country-wide campaign with the new vaccine in late 2010 and before the onset of the next epidemic meningococcal disease season beginning in January 2011. In the ensuing five months (July-November 2010) the following challenges were successfully managed: (1) doing a large safety study and registering the new vaccine in Burkina Faso; (2) developing a comprehensive communication plan; (3) strengthening the surveillance system with particular attention to improving the capacity for real-time polymerase chain reaction (PCR) testing of spinal fluid specimens; (4) improving cold chain capacity and waste disposal; (5) developing and funding a sound campaign strategy; and (6) ensuring effective collaboration across all partners. Each of these issues required specific strategies that were managed through a WHO-led consortium that included all major partners (Ministry of Health/Burkina Faso, Serum Institute of India Ltd., UNICEF, Global Alliance for Vaccines and Immunization, Meningitis Vaccine Project, CDC/Atlanta, and the Norwegian Institute of Public Health/Oslo). Biweekly teleconferences that were led by WHO ensured that problems were identified in a timely fashion. The new meningococcal A conjugate vaccine was introduced on December 6, 2010, in a national ceremony led by His Excellency Blaise Compaore, the President of Burkina Faso. The ensuing 10-day national campaign was hugely successful, and over 11.4 million Burkinabes between the ages of 1 and 29 years (100% of target population) were vaccinated. African national immunization programs are capable of achieving very high coverage for a vaccine desired by the public, introduced in a well-organized campaign, and supported at the highest political level. The Burkina Faso success augurs well for further rollout of the Men A conjugate vaccine in meningitis belt countries.
The Journal of Infectious Diseases | 2009
A. Duncan Steele; Manish M. Patel; Umesh D. Parashar; John C. Victor; Teresa Aguado; Kathleen M. Neuzil
The World Health Organization (WHO) and its international partners have prioritized the development of rotavirus vaccines for the past 3 decades. In November 2005, the WHOs Strategic Advisory Group of Experts first reviewed the clinical efficacy data from 2 new live attenuated oral rotavirus vaccines, which demonstrated excellent protective efficacy against severe rotavirus disease in regions where they were evaluated. Despite these successes, the WHO has urged the clinical evaluation of these vaccines in populations of Africa and Asia, where most of the deaths due to rotavirus occur, and has emphasized the need for ongoing postlicensure safety monitoring in countries introducing vaccines. Clinical studies in Africa and Asia will soon provide data on the efficacy of both new vaccines in these populations. A WHO international consultative meeting convened to evaluate how to use these imminent data for the future use of rotavirus vaccines in developing countries. In brief, it was agreed that (1) even vaccines with lesser efficacy in developing countries, compared with industrialized countries, would still lead to substantial public health benefits and would be cost-effective in saving lives in Africa and Asia; (2) criteria, such as the WHO mortality strata and local epidemiology of rotavirus infection, would be appropriate measures for extrapolating the clinical data to other regions and countries; and (3) research toward understanding the programmatic limitations of rotavirus vaccine use may help develop strategies to improve vaccine uptake and overall impact.
Seminars in Pediatric Infectious Diseases | 2003
Philippe Duclos; Alison Delo; Teresa Aguado; Julian Bilous; Maureen Birmingham; Marie Paule Kieny; Julie Milstien; David Wood; Daniel Tarantola
In 1999, the World Health Organizations (WHO) Department of Vaccines and Biologicals launched the Immunization Safety Priority Project with the aim of establishing a comprehensive system to ensure the safety of all immunizations given in national immunization programs. Countries are the primary focus of the project. WHO has a role, not only because of its technical and normative role, but also because of its privileged relationship with country authorities and other partners, and its global vision and mandate. The four major areas of focus in the project are to (1) promote and coordinate research and development of safer and simpler delivery systems; (2) ensure vaccine safety, from vaccine development all the way through clinical trials and vaccine distribution until use; (3) broaden access to safer and more efficient systems for vaccine delivery and management of sharps waste; and (4) establish efficient mechanisms to detect serious or potentially serious adverse events following immunization, and enable prompt and effective response. The project emphasizes the importance of advocating safety and building capacity at national levels.
Vaccine | 2007
Richard I. Walker; Duncan Steele; Teresa Aguado
Vaccine | 2006
Mark Kane; Jacqueline Sherris; Pierre Coursaget; Teresa Aguado; Felicity Cutts
Vaccine | 2006
Mark Kane; Jacqueline Sherris; Pierre Coursaget; Teresa Aguado; Felicity Cutts
Procedia in Vaccinology | 2010
Ana Maria Henao-Restrepo; Michel Greco; Ximena Laurie; Oommen John; Teresa Aguado
Journal of Autoimmunity | 1993
Giulia Kramar; Stephane Schurmans; Teresa Aguado; Shozo Izui; Giuseppe Del Giudice; Paul Henri Lambert
European Journal of Immunology | 1993
Giulia Kramar; Teresa Aguado; Jacques A. Louis; Giuseppe Del Giudice; Paul-Henri Lambert