2022
DOI: 10.1172/jci.insight.160173
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Effectiveness of CHIKV vaccine VLA1553 demonstrated by passive transfer of human sera

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Cited by 28 publications
(22 citation statements)
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References 47 publications
(69 reference statements)
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“…132,200). A three-dose phase I trial of VLA1553 found that low and medium vaccine doses were well tolerated and immunogenic; encouragingly, there was no discernible immune response following the third dose, suggesting that vaccinated participants were protected against, essentially, a repeat viral challenge (for example, had sterilizing immunity) 201,202 . Follow-up studies in mice and non-human primates demonstrated that passive transfer of serum samples from the VLA1553 phase I study led to protection against CHIKV challenge 200 .…”
Section: Vaccine-based Prevention Of Chikungunya Fevermentioning
confidence: 99%
See 1 more Smart Citation
“…132,200). A three-dose phase I trial of VLA1553 found that low and medium vaccine doses were well tolerated and immunogenic; encouragingly, there was no discernible immune response following the third dose, suggesting that vaccinated participants were protected against, essentially, a repeat viral challenge (for example, had sterilizing immunity) 201,202 . Follow-up studies in mice and non-human primates demonstrated that passive transfer of serum samples from the VLA1553 phase I study led to protection against CHIKV challenge 200 .…”
Section: Vaccine-based Prevention Of Chikungunya Fevermentioning
confidence: 99%
“…In 2022, the results of a USA-based randomized controlled trial of VLA1553 showed that nearly 100% of participants, including persons aged 65 or older, had met the proposed threshold for seroprotection after a single dose, and the vaccine was deemed safe and well tolerated 202 . Follow-up on a subgroup of participants will continue for 5 years and an additional trial in adolescents is under way in Brazil, with the hope that it may be one of the first countries in an endemic area to provide approval.…”
Section: Vaccine-based Prevention Of Chikungunya Fevermentioning
confidence: 99%
“…VLA1553 was first investigated as part of a collaborative European research consortium (ICRES FP7-HEALTH project; https://cordis.europa.eu/project/id/261202). The vaccine is a monovalent, single-dose, live-attenuated vaccine for humans that received Fast Track designation from the FDA in December 2018 [44, 45].…”
Section: Methodsmentioning
confidence: 99%
“…67,68 The ∆5nsP3 virus showed a very good safety profile and efficacy in mice and cynomolgus macaques 69 and has undergone clinical testing by Valneva. 70 The company recently successfully completed a Phase III trial (NCT04546724) (Table 1). The trial analysis showed that 98.9% of participants achieved protective levels of CHIKV-neutralizing antibodies one month after receiving a single vaccination, and 96.3% of participants had protective CHIKVneutralizing antibody titers six months after receiving a single vaccination (Valneva, press release).…”
Section: Live-attenuated Virusesmentioning
confidence: 99%