Interpreting challenge data from early phase malaria blood stage vaccine trials

Introduction: As the quest for an effective blood stage malaria vaccine continues, there is increasing reliance on the use of controlled human malaria infections (CHMI) in non-endemic settings to test vaccine efficacy at the earliest possible time. This is seen as a way to accelerate vaccine researc...

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Main Authors: Michael F. Good, Louis H. Miller
Format: Article
Language:English
Published: Taylor & Francis Group 2018-03-01
Series:Expert Review of Vaccines
Subjects:
Online Access:http://dx.doi.org/10.1080/14760584.2018.1435278
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author Michael F. Good
Louis H. Miller
author_facet Michael F. Good
Louis H. Miller
author_sort Michael F. Good
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description Introduction: As the quest for an effective blood stage malaria vaccine continues, there is increasing reliance on the use of controlled human malaria infections (CHMI) in non-endemic settings to test vaccine efficacy at the earliest possible time. This is seen as a way to accelerate vaccine research and quickly eliminate candidates with poor efficacy. Areas covered: The data from these studies need to be carefully examined and interpreted in light of the very different roles that antibody and cellular immunity play in protection and within the context of the distinct clinical sensitivities of volunteers living in malaria-non-endemic countries compared to those living in endemic countries. With current strategies, it is likely that vaccines with protective immunological ‘signatures’ will be missed and potentially good candidates discarded. Expert commentary: Efficacy data from early phase vaccine trials in non-endemic countries should not be used to decide whether or not to proceed to vaccine trials in endemic countries.
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spelling doaj.art-0e19cf177682415993fbc6f32d5405792023-09-20T10:18:03ZengTaylor & Francis GroupExpert Review of Vaccines1476-05841744-83952018-03-0117318919610.1080/14760584.2018.14352781435278Interpreting challenge data from early phase malaria blood stage vaccine trialsMichael F. Good0Louis H. Miller1Griffith UniversityNational Institutes of HealthIntroduction: As the quest for an effective blood stage malaria vaccine continues, there is increasing reliance on the use of controlled human malaria infections (CHMI) in non-endemic settings to test vaccine efficacy at the earliest possible time. This is seen as a way to accelerate vaccine research and quickly eliminate candidates with poor efficacy. Areas covered: The data from these studies need to be carefully examined and interpreted in light of the very different roles that antibody and cellular immunity play in protection and within the context of the distinct clinical sensitivities of volunteers living in malaria-non-endemic countries compared to those living in endemic countries. With current strategies, it is likely that vaccines with protective immunological ‘signatures’ will be missed and potentially good candidates discarded. Expert commentary: Efficacy data from early phase vaccine trials in non-endemic countries should not be used to decide whether or not to proceed to vaccine trials in endemic countries.http://dx.doi.org/10.1080/14760584.2018.1435278malaria vaccinessub-unit vaccineswhole parasite vaccinescellular immunityantibody-mediated immunitychmi
spellingShingle Michael F. Good
Louis H. Miller
Interpreting challenge data from early phase malaria blood stage vaccine trials
Expert Review of Vaccines
malaria vaccines
sub-unit vaccines
whole parasite vaccines
cellular immunity
antibody-mediated immunity
chmi
title Interpreting challenge data from early phase malaria blood stage vaccine trials
title_full Interpreting challenge data from early phase malaria blood stage vaccine trials
title_fullStr Interpreting challenge data from early phase malaria blood stage vaccine trials
title_full_unstemmed Interpreting challenge data from early phase malaria blood stage vaccine trials
title_short Interpreting challenge data from early phase malaria blood stage vaccine trials
title_sort interpreting challenge data from early phase malaria blood stage vaccine trials
topic malaria vaccines
sub-unit vaccines
whole parasite vaccines
cellular immunity
antibody-mediated immunity
chmi
url http://dx.doi.org/10.1080/14760584.2018.1435278
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