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Controlled Human Infection Models To Accelerate Vaccine Development.
Choy, Robert K M; Bourgeois, A Louis; Ockenhouse, Christian F; Walker, Richard I; Sheets, Rebecca L; Flores, Jorge.
Afiliação
  • Choy RKM; PATH, Center for Vaccine Innovation and Access, Seattle, Washington, USA.
  • Bourgeois AL; PATH, Center for Vaccine Innovation and Access, Seattle, Washington, USA.
  • Ockenhouse CF; PATH, Center for Vaccine Innovation and Access, Seattle, Washington, USA.
  • Walker RI; PATH, Center for Vaccine Innovation and Access, Seattle, Washington, USA.
  • Sheets RL; Grimalkin Partners, Silver Spring, Maryland, USA.
  • Flores J; PATH, Center for Vaccine Innovation and Access, Seattle, Washington, USA.
Clin Microbiol Rev ; 35(3): e0000821, 2022 09 21.
Article em En | MEDLINE | ID: mdl-35862754
ABSTRACT
The timelines for developing vaccines against infectious diseases are lengthy, and often vaccines that reach the stage of large phase 3 field trials fail to provide the desired level of protective efficacy. The application of controlled human challenge models of infection and disease at the appropriate stages of development could accelerate development of candidate vaccines and, in fact, has done so successfully in some limited cases. Human challenge models could potentially be used to gather critical information on pathogenesis, inform strain selection for vaccines, explore cross-protective immunity, identify immune correlates of protection and mechanisms of protection induced by infection or evoked by candidate vaccines, guide decisions on appropriate trial endpoints, and evaluate vaccine efficacy. We prepared this report to motivate fellow scientists to exploit the potential capacity of controlled human challenge experiments to advance vaccine development. In this review, we considered available challenge models for 17 infectious diseases in the context of the public health importance of each disease, the diversity and pathogenesis of the causative organisms, the vaccine candidates under development, and each model's capacity to evaluate them and identify correlates of protective immunity. Our broad assessment indicated that human challenge models have not yet reached their full potential to support the development of vaccines against infectious diseases. On the basis of our review, however, we believe that describing an ideal challenge model is possible, as is further developing existing and future challenge models.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Desenvolvimento de Vacinas / Modelos Biológicos Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Desenvolvimento de Vacinas / Modelos Biológicos Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article