Development of novel vaccine candidates and challenge models for Plasmodium vivax

Plasmodium vivax is the most widely distributed human malaria parasite in the world and despite nearly 2.5 billion people living at risk, only four vaccines have been assessed in phase I clinical trials and only one has progressed to a phase II trial showing no sterile efficacy. We started to develo...

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Main Authors: Alves, E, Salman, A, Janse, C, Khan, S, Hill, A, Reyes-Sandoval, A
Format: Journal article
Published: BioMed Central 2014
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author Alves, E
Salman, A
Janse, C
Khan, S
Hill, A
Reyes-Sandoval, A
author_facet Alves, E
Salman, A
Janse, C
Khan, S
Hill, A
Reyes-Sandoval, A
author_sort Alves, E
collection OXFORD
description Plasmodium vivax is the most widely distributed human malaria parasite in the world and despite nearly 2.5 billion people living at risk, only four vaccines have been assessed in phase I clinical trials and only one has progressed to a phase II trial showing no sterile efficacy. We started to develop new challenge models to assess the efficacy of several new P. vivax pre-erythrocytic vaccine candidates (PVX_091700; PVX_121950; PVX_084090; PVX_099035; PVX_095375; PVX_000975; PVX_003665; PVX_000810) in mice. Our model is based on creating mutant P. berghei (rodent malaria) lines expressing P. vivax antigens through a new method called “Gene Insertion/Marker out” (GIMO). In addition, we are cloning the P. vivax pre-erythrocytic vaccine candidates in recombinant chimpanzee adenovirus (ChAd) and modified vaccine Ankara (MVA) vectors. Upon generation of transgenic parasites and recombinant viruses, a faster assessment to determinate the efficacy of all new P. vivax vaccine candidates can be achieved by using prime/boost immunization regimens followed by a challenge with corresponding transgenic chimera parasites.
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spelling oxford-uuid:42bff3da-4c40-4fb8-ab15-811aa2095c672022-03-26T14:51:16ZDevelopment of novel vaccine candidates and challenge models for Plasmodium vivaxJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:42bff3da-4c40-4fb8-ab15-811aa2095c67Symplectic Elements at OxfordBioMed Central2014Alves, ESalman, AJanse, CKhan, SHill, AReyes-Sandoval, APlasmodium vivax is the most widely distributed human malaria parasite in the world and despite nearly 2.5 billion people living at risk, only four vaccines have been assessed in phase I clinical trials and only one has progressed to a phase II trial showing no sterile efficacy. We started to develop new challenge models to assess the efficacy of several new P. vivax pre-erythrocytic vaccine candidates (PVX_091700; PVX_121950; PVX_084090; PVX_099035; PVX_095375; PVX_000975; PVX_003665; PVX_000810) in mice. Our model is based on creating mutant P. berghei (rodent malaria) lines expressing P. vivax antigens through a new method called “Gene Insertion/Marker out” (GIMO). In addition, we are cloning the P. vivax pre-erythrocytic vaccine candidates in recombinant chimpanzee adenovirus (ChAd) and modified vaccine Ankara (MVA) vectors. Upon generation of transgenic parasites and recombinant viruses, a faster assessment to determinate the efficacy of all new P. vivax vaccine candidates can be achieved by using prime/boost immunization regimens followed by a challenge with corresponding transgenic chimera parasites.
spellingShingle Alves, E
Salman, A
Janse, C
Khan, S
Hill, A
Reyes-Sandoval, A
Development of novel vaccine candidates and challenge models for Plasmodium vivax
title Development of novel vaccine candidates and challenge models for Plasmodium vivax
title_full Development of novel vaccine candidates and challenge models for Plasmodium vivax
title_fullStr Development of novel vaccine candidates and challenge models for Plasmodium vivax
title_full_unstemmed Development of novel vaccine candidates and challenge models for Plasmodium vivax
title_short Development of novel vaccine candidates and challenge models for Plasmodium vivax
title_sort development of novel vaccine candidates and challenge models for plasmodium vivax
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