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Target product profile for a dengue pre-vaccination screening test.
Fongwen, Noah; Wilder-Smith, Annelise; Gubler, Duane J; Ooi, Eng Eong; T Salvana, Edsel Maurice; de Lamballerie, Xavier; Olliaro, Piero L; Peeling, Rosanna W.
Afiliação
  • Fongwen N; International Diagnostics Centre, Department of Clinical Research, London School of Hygiene and Tropical Medicine, London, United Kingdom.
  • Wilder-Smith A; Heidelberg Institute of Global Health, University of Heidelberg, Germany.
  • Gubler DJ; Institute of Social and Preventive Medicine, University of Bern, Switzerland.
  • Ooi EE; Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore.
  • T Salvana EM; Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore.
  • de Lamballerie X; Institute of Molecular Biology and Biotechnology, National Institutes of Health, University of the Philippines Manila, Manila, Philippines.
  • Olliaro PL; Unité des Virus Emergents (UVE), Aix Marseille Université, IRD 190, INSERM 1207, IHU Méditerranée Infection, Marseille, France.
  • Peeling RW; Centre for Tropical Medicine and Global Health, University of Oxford, Oxford, United Kingdom.
PLoS Negl Trop Dis ; 15(7): e0009557, 2021 07.
Article em En | MEDLINE | ID: mdl-34324505
ABSTRACT
With increasing geographic spread, frequency, and magnitude of outbreaks, dengue continues to pose a major public health threat worldwide. Dengvaxia, a dengue live-attenuated tetravalent vaccine, was licensed in 2015, but post hoc analyses of long-term data showed serostatus-dependent vaccine performance with an excess risk of hospitalized and severe dengue in seronegative vaccine recipients. The World Health Organization (WHO) recommended that only persons with evidence of past dengue infection should receive the vaccine. A test for pre-vaccination screening for dengue serostatus is needed. To develop the target product profile (TPP) for a dengue pre-vaccination screening test, face-to-face consultative meetings were organized with follow-up regional consultations. A technical working group was formed to develop consensus on a reference test against which candidate pre-vaccination screening tests could be compared. The group also reviewed current diagnostic landscape and the need to accelerate the evaluation, regulatory approval, and policy development of tests that can identify seropositive individuals and maximize public health impact of vaccination while avoiding the risk of hospitalization in dengue-naive individuals. Pre-vaccination screening strategies will benefit from rapid diagnostic tests (RDTs) that are affordable, sensitive, and specific and can be used at the point of care (POC). The TPP described the minimum and ideal characteristics of a dengue pre-vaccination screening RDT with an emphasis on high specificity. The group also made suggestions for accelerating access to these RDTs through streamlining regulatory approval and policy development. Risk and benefit based on what can be achieved with RDTs meeting minimal and optimal characteristics in the TPP across a range of seroprevalences were defined. The final choice of RDTs in each country will depend on the performance of the RDT, dengue seroprevalence in the target population, tolerance of risk, and cost-effectiveness.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Testes Sorológicos / Vacinação / Dengue / Vacinas contra Dengue / Testes Imediatos Tipo de estudo: Diagnostic_studies / Prognostic_studies / Screening_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Testes Sorológicos / Vacinação / Dengue / Vacinas contra Dengue / Testes Imediatos Tipo de estudo: Diagnostic_studies / Prognostic_studies / Screening_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article