Cargando…
Safety and immunogenicity of AGS-v PLUS, a mosquito saliva peptide vaccine against arboviral diseases: A randomized, double-blind, placebo-controlled Phase 1 trial
BACKGROUND: Immunity to mosquito salivary proteins could provide protection against multiple mosquito-borne diseases and significantly impact public health. We evaluated the safety and immunogenicity of AGS-v PLUS, a mosquito salivary peptide vaccine, in healthy adults 18–50 years old. METHODS: We c...
Autores principales: | , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9700263/ https://www.ncbi.nlm.nih.gov/pubmed/36436281 http://dx.doi.org/10.1016/j.ebiom.2022.104375 |
_version_ | 1784839271140556800 |
---|---|
author | Friedman-Klabanoff, DeAnna J. Birkhold, Megan Short, Mara T. Wilson, Timothy R. Meneses, Claudio R. Lacsina, Joshua R. Oliveira, Fabiano Kamhawi, Shaden Valenzuela, Jesus G. Hunsberger, Sally Mateja, Allyson Stoloff, Gregory Pleguezuelos, Olga Memoli, Matthew J. Laurens, Matthew B. |
author_facet | Friedman-Klabanoff, DeAnna J. Birkhold, Megan Short, Mara T. Wilson, Timothy R. Meneses, Claudio R. Lacsina, Joshua R. Oliveira, Fabiano Kamhawi, Shaden Valenzuela, Jesus G. Hunsberger, Sally Mateja, Allyson Stoloff, Gregory Pleguezuelos, Olga Memoli, Matthew J. Laurens, Matthew B. |
author_sort | Friedman-Klabanoff, DeAnna J. |
collection | PubMed |
description | BACKGROUND: Immunity to mosquito salivary proteins could provide protection against multiple mosquito-borne diseases and significantly impact public health. We evaluated the safety and immunogenicity of AGS-v PLUS, a mosquito salivary peptide vaccine, in healthy adults 18–50 years old. METHODS: We conducted a randomized, double-blind, placebo-controlled Phase 1 study of AGS-v PLUS administered subcutaneously on Days 1 and 22 at the Center for Vaccine Development and Global Health, Baltimore, MD, USA. Participants were block randomized 1:1:1:1:1 to two doses saline placebo, two doses AGS-v PLUS, AGS-v PLUS/ISA-51 and saline placebo, two doses AGS-v PLUS/ISA-51, or two doses AGS-v PLUS/Alhydrogel. Primary endpoints were safety (all participants receiving ≥1 injection) and antibody and cytokine responses (all participants with day 43 samples), analysed by intention to treat. FINDINGS: Between 26 August 2019 and 25 February 2020, 51 participants were enrolled and randomized, 11 into the single dose AGS-v PLUS/ISA-51 group and ten in other groups. Due to COVID-19, 15 participants did not return for day 43 samplings. Participants experienced no treatment-emergent or serious adverse events. All solicited symptoms in 2/10 placebo recipients and 22/41 AGS-v PLUS recipients after dose one and 1/10 placebo recipients and 22/41 AGS-v PLUS recipients after dose two were mild/moderate except for one severe fever the day after vaccination (placebo group). Only injection site pain was more common in vaccine groups (15/51 after dose 1 and 11/51 after dose 2) versus placebo. Compared to placebo, all vaccine groups had significantly greater fold change in anti-AGS-v PLUS IgG and IFN-ɣ from baseline. INTERPRETATION: AGS-v PLUS had favourable safety profile and induced robust immune responses. Next steps will determine if findings translate into clinical efficacy against mosquito-borne diseases. FUNDING: 10.13039/501100000276UK Department of Health and Social Care. |
format | Online Article Text |
id | pubmed-9700263 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-97002632022-11-27 Safety and immunogenicity of AGS-v PLUS, a mosquito saliva peptide vaccine against arboviral diseases: A randomized, double-blind, placebo-controlled Phase 1 trial Friedman-Klabanoff, DeAnna J. Birkhold, Megan Short, Mara T. Wilson, Timothy R. Meneses, Claudio R. Lacsina, Joshua R. Oliveira, Fabiano Kamhawi, Shaden Valenzuela, Jesus G. Hunsberger, Sally Mateja, Allyson Stoloff, Gregory Pleguezuelos, Olga Memoli, Matthew J. Laurens, Matthew B. eBioMedicine Articles BACKGROUND: Immunity to mosquito salivary proteins could provide protection against multiple mosquito-borne diseases and significantly impact public health. We evaluated the safety and immunogenicity of AGS-v PLUS, a mosquito salivary peptide vaccine, in healthy adults 18–50 years old. METHODS: We conducted a randomized, double-blind, placebo-controlled Phase 1 study of AGS-v PLUS administered subcutaneously on Days 1 and 22 at the Center for Vaccine Development and Global Health, Baltimore, MD, USA. Participants were block randomized 1:1:1:1:1 to two doses saline placebo, two doses AGS-v PLUS, AGS-v PLUS/ISA-51 and saline placebo, two doses AGS-v PLUS/ISA-51, or two doses AGS-v PLUS/Alhydrogel. Primary endpoints were safety (all participants receiving ≥1 injection) and antibody and cytokine responses (all participants with day 43 samples), analysed by intention to treat. FINDINGS: Between 26 August 2019 and 25 February 2020, 51 participants were enrolled and randomized, 11 into the single dose AGS-v PLUS/ISA-51 group and ten in other groups. Due to COVID-19, 15 participants did not return for day 43 samplings. Participants experienced no treatment-emergent or serious adverse events. All solicited symptoms in 2/10 placebo recipients and 22/41 AGS-v PLUS recipients after dose one and 1/10 placebo recipients and 22/41 AGS-v PLUS recipients after dose two were mild/moderate except for one severe fever the day after vaccination (placebo group). Only injection site pain was more common in vaccine groups (15/51 after dose 1 and 11/51 after dose 2) versus placebo. Compared to placebo, all vaccine groups had significantly greater fold change in anti-AGS-v PLUS IgG and IFN-ɣ from baseline. INTERPRETATION: AGS-v PLUS had favourable safety profile and induced robust immune responses. Next steps will determine if findings translate into clinical efficacy against mosquito-borne diseases. FUNDING: 10.13039/501100000276UK Department of Health and Social Care. Elsevier 2022-11-24 /pmc/articles/PMC9700263/ /pubmed/36436281 http://dx.doi.org/10.1016/j.ebiom.2022.104375 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Articles Friedman-Klabanoff, DeAnna J. Birkhold, Megan Short, Mara T. Wilson, Timothy R. Meneses, Claudio R. Lacsina, Joshua R. Oliveira, Fabiano Kamhawi, Shaden Valenzuela, Jesus G. Hunsberger, Sally Mateja, Allyson Stoloff, Gregory Pleguezuelos, Olga Memoli, Matthew J. Laurens, Matthew B. Safety and immunogenicity of AGS-v PLUS, a mosquito saliva peptide vaccine against arboviral diseases: A randomized, double-blind, placebo-controlled Phase 1 trial |
title | Safety and immunogenicity of AGS-v PLUS, a mosquito saliva peptide vaccine against arboviral diseases: A randomized, double-blind, placebo-controlled Phase 1 trial |
title_full | Safety and immunogenicity of AGS-v PLUS, a mosquito saliva peptide vaccine against arboviral diseases: A randomized, double-blind, placebo-controlled Phase 1 trial |
title_fullStr | Safety and immunogenicity of AGS-v PLUS, a mosquito saliva peptide vaccine against arboviral diseases: A randomized, double-blind, placebo-controlled Phase 1 trial |
title_full_unstemmed | Safety and immunogenicity of AGS-v PLUS, a mosquito saliva peptide vaccine against arboviral diseases: A randomized, double-blind, placebo-controlled Phase 1 trial |
title_short | Safety and immunogenicity of AGS-v PLUS, a mosquito saliva peptide vaccine against arboviral diseases: A randomized, double-blind, placebo-controlled Phase 1 trial |
title_sort | safety and immunogenicity of ags-v plus, a mosquito saliva peptide vaccine against arboviral diseases: a randomized, double-blind, placebo-controlled phase 1 trial |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9700263/ https://www.ncbi.nlm.nih.gov/pubmed/36436281 http://dx.doi.org/10.1016/j.ebiom.2022.104375 |
work_keys_str_mv | AT friedmanklabanoffdeannaj safetyandimmunogenicityofagsvplusamosquitosalivapeptidevaccineagainstarboviraldiseasesarandomizeddoubleblindplacebocontrolledphase1trial AT birkholdmegan safetyandimmunogenicityofagsvplusamosquitosalivapeptidevaccineagainstarboviraldiseasesarandomizeddoubleblindplacebocontrolledphase1trial AT shortmarat safetyandimmunogenicityofagsvplusamosquitosalivapeptidevaccineagainstarboviraldiseasesarandomizeddoubleblindplacebocontrolledphase1trial AT wilsontimothyr safetyandimmunogenicityofagsvplusamosquitosalivapeptidevaccineagainstarboviraldiseasesarandomizeddoubleblindplacebocontrolledphase1trial AT menesesclaudior safetyandimmunogenicityofagsvplusamosquitosalivapeptidevaccineagainstarboviraldiseasesarandomizeddoubleblindplacebocontrolledphase1trial AT lacsinajoshuar safetyandimmunogenicityofagsvplusamosquitosalivapeptidevaccineagainstarboviraldiseasesarandomizeddoubleblindplacebocontrolledphase1trial AT oliveirafabiano safetyandimmunogenicityofagsvplusamosquitosalivapeptidevaccineagainstarboviraldiseasesarandomizeddoubleblindplacebocontrolledphase1trial AT kamhawishaden safetyandimmunogenicityofagsvplusamosquitosalivapeptidevaccineagainstarboviraldiseasesarandomizeddoubleblindplacebocontrolledphase1trial AT valenzuelajesusg safetyandimmunogenicityofagsvplusamosquitosalivapeptidevaccineagainstarboviraldiseasesarandomizeddoubleblindplacebocontrolledphase1trial AT hunsbergersally safetyandimmunogenicityofagsvplusamosquitosalivapeptidevaccineagainstarboviraldiseasesarandomizeddoubleblindplacebocontrolledphase1trial AT matejaallyson safetyandimmunogenicityofagsvplusamosquitosalivapeptidevaccineagainstarboviraldiseasesarandomizeddoubleblindplacebocontrolledphase1trial AT stoloffgregory safetyandimmunogenicityofagsvplusamosquitosalivapeptidevaccineagainstarboviraldiseasesarandomizeddoubleblindplacebocontrolledphase1trial AT pleguezuelosolga safetyandimmunogenicityofagsvplusamosquitosalivapeptidevaccineagainstarboviraldiseasesarandomizeddoubleblindplacebocontrolledphase1trial AT memolimatthewj safetyandimmunogenicityofagsvplusamosquitosalivapeptidevaccineagainstarboviraldiseasesarandomizeddoubleblindplacebocontrolledphase1trial AT laurensmatthewb safetyandimmunogenicityofagsvplusamosquitosalivapeptidevaccineagainstarboviraldiseasesarandomizeddoubleblindplacebocontrolledphase1trial |