Abstract
Chikungunya virus infection causes a debilitating febrile illness that in many affected individuals is associated with long-term sequelae that can persist for months or years. Over the past decade a large number of candidate vaccines have been developed, several of which have now entered clinical trials. The rapid and sporadic nature of chikungunya outbreaks poses challenges for planning of large clinical efficacy trials suggesting that licensure of chikungunya vaccines may utilize non-traditional approval pathways based on identification of immunological endpoint(s) predictive of clinical benefit. This report reviews the current status of nonclinical and clinical testing and potential challenges for defining a suitable surrogate or correlate of protection.
Original language | English (US) |
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Pages (from-to) | 7427-7436 |
Number of pages | 10 |
Journal | Vaccine |
Volume | 37 |
Issue number | 50 |
DOIs | |
State | Published - Nov 28 2019 |
Keywords
- Animal models
- Arbovirus
- Assays
- Clinical trial
- Neutralizing antibodies
- Vaccine
ASJC Scopus subject areas
- Molecular Medicine
- General Immunology and Microbiology
- General Veterinary
- Public Health, Environmental and Occupational Health
- Infectious Diseases