Adjuvanting a viral vectored vaccine against pre-erythrocytic malaria
Abstract The majority of routinely given vaccines require two or three immunisations for full protective efficacy. Single dose vaccination has long been considered a key solution to improving the global immunisation coverage. Recent infectious disease outbreaks have further highlighted the need for...
Guardado en:
Autores principales: | , , , , , |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2017
|
Materias: | |
Acceso en línea: | https://doaj.org/article/f74c5ffaca3348a884a9626d718f804a |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
id |
oai:doaj.org-article:f74c5ffaca3348a884a9626d718f804a |
---|---|
record_format |
dspace |
spelling |
oai:doaj.org-article:f74c5ffaca3348a884a9626d718f804a2021-12-02T12:32:21ZAdjuvanting a viral vectored vaccine against pre-erythrocytic malaria10.1038/s41598-017-07246-02045-2322https://doaj.org/article/f74c5ffaca3348a884a9626d718f804a2017-08-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-07246-0https://doaj.org/toc/2045-2322Abstract The majority of routinely given vaccines require two or three immunisations for full protective efficacy. Single dose vaccination has long been considered a key solution to improving the global immunisation coverage. Recent infectious disease outbreaks have further highlighted the need for vaccines that can achieve full efficacy after a single administration. Viral vectors are a potent immunisation platform, benefiting from intrinsic immuno-stimulatory features while retaining excellent safety profile through the use of non-replicating viruses. We investigated the scope for enhancing the protective efficacy of a single dose adenovirus-vectored malaria vaccine in a mouse model of malaria by co-administering it with vaccine adjuvants. Out of 11 adjuvants, only two, Abisco®-100 and CoVaccineHTTM, enhanced vaccine efficacy and sterile protection following malaria challenge. The CoVaccineHTTM adjuvanted vaccine induced significantly higher proportion of antigen specific central memory CD8+ cells, and both adjuvants resulted in increased proportion of CD8+ T cells expressing the CD107a degranulation marker in the absence of IFNγ, TNFα and IL2 production. Our results show that the efficacy of vaccines designed to induce protective T cell responses can be positively modulated with chemical adjuvants and open the possibility of achieving full protection with a single dose immunisation.Anita MilicicChristine S. RollierChoon Kit TangRhea LongleyAdrian V. S. HillArturo Reyes-SandovalNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-12 (2017) |
institution |
DOAJ |
collection |
DOAJ |
language |
EN |
topic |
Medicine R Science Q |
spellingShingle |
Medicine R Science Q Anita Milicic Christine S. Rollier Choon Kit Tang Rhea Longley Adrian V. S. Hill Arturo Reyes-Sandoval Adjuvanting a viral vectored vaccine against pre-erythrocytic malaria |
description |
Abstract The majority of routinely given vaccines require two or three immunisations for full protective efficacy. Single dose vaccination has long been considered a key solution to improving the global immunisation coverage. Recent infectious disease outbreaks have further highlighted the need for vaccines that can achieve full efficacy after a single administration. Viral vectors are a potent immunisation platform, benefiting from intrinsic immuno-stimulatory features while retaining excellent safety profile through the use of non-replicating viruses. We investigated the scope for enhancing the protective efficacy of a single dose adenovirus-vectored malaria vaccine in a mouse model of malaria by co-administering it with vaccine adjuvants. Out of 11 adjuvants, only two, Abisco®-100 and CoVaccineHTTM, enhanced vaccine efficacy and sterile protection following malaria challenge. The CoVaccineHTTM adjuvanted vaccine induced significantly higher proportion of antigen specific central memory CD8+ cells, and both adjuvants resulted in increased proportion of CD8+ T cells expressing the CD107a degranulation marker in the absence of IFNγ, TNFα and IL2 production. Our results show that the efficacy of vaccines designed to induce protective T cell responses can be positively modulated with chemical adjuvants and open the possibility of achieving full protection with a single dose immunisation. |
format |
article |
author |
Anita Milicic Christine S. Rollier Choon Kit Tang Rhea Longley Adrian V. S. Hill Arturo Reyes-Sandoval |
author_facet |
Anita Milicic Christine S. Rollier Choon Kit Tang Rhea Longley Adrian V. S. Hill Arturo Reyes-Sandoval |
author_sort |
Anita Milicic |
title |
Adjuvanting a viral vectored vaccine against pre-erythrocytic malaria |
title_short |
Adjuvanting a viral vectored vaccine against pre-erythrocytic malaria |
title_full |
Adjuvanting a viral vectored vaccine against pre-erythrocytic malaria |
title_fullStr |
Adjuvanting a viral vectored vaccine against pre-erythrocytic malaria |
title_full_unstemmed |
Adjuvanting a viral vectored vaccine against pre-erythrocytic malaria |
title_sort |
adjuvanting a viral vectored vaccine against pre-erythrocytic malaria |
publisher |
Nature Portfolio |
publishDate |
2017 |
url |
https://doaj.org/article/f74c5ffaca3348a884a9626d718f804a |
work_keys_str_mv |
AT anitamilicic adjuvantingaviralvectoredvaccineagainstpreerythrocyticmalaria AT christinesrollier adjuvantingaviralvectoredvaccineagainstpreerythrocyticmalaria AT choonkittang adjuvantingaviralvectoredvaccineagainstpreerythrocyticmalaria AT rhealongley adjuvantingaviralvectoredvaccineagainstpreerythrocyticmalaria AT adrianvshill adjuvantingaviralvectoredvaccineagainstpreerythrocyticmalaria AT arturoreyessandoval adjuvantingaviralvectoredvaccineagainstpreerythrocyticmalaria |
_version_ |
1718394132696662016 |