作者
Todd J Suscovich, Jonathan K Fallon, Jishnu Das, Allison R Demas, Jonathan Crain, Caitlyn H Linde, Ashlin Michell, Harini Natarajan, Claudia Arevalo, Thomas Broge, Thomas Linnekin, Viraj Kulkarni, Richard Lu, Matthew D Slein, Corinne Luedemann, Meghan Marquette, Sandra March, Joshua Weiner, Scott Gregory, Margherita Coccia, Yevel Flores-Garcia, Fidel Zavala, Margaret E Ackerman, Elke Bergmann-Leitner, Jenny Hendriks, Jerald Sadoff, Sheetij Dutta, Sangeeta N Bhatia, Douglas A Lauffenburger, Erik Jongert, Ulrike Wille-Reece, Galit Alter
发表日期
2020/7/22
期刊
Science translational medicine
卷号
12
期号
553
页码范围
eabb4757
出版商
American Association for the Advancement of Science
简介
Vaccine development has the potential to be accelerated by coupling tools such as systems immunology analyses and controlled human infection models to define the protective efficacy of prospective immunogens without expensive and slow phase 2b/3 vaccine studies. Among human challenge models, controlled human malaria infection trials have long been used to evaluate candidate vaccines, and RTS,S/AS01 is the most advanced malaria vaccine candidate, reproducibly demonstrating 40 to 80% protection in human challenge studies in malaria-naïve individuals. Although antibodies are critical for protection after RTS,S/AS01 vaccination, antibody concentrations are inconsistently associated with protection across studies, and the precise mechanism(s) by which vaccine-induced antibodies provide protection remains enigmatic. Using a comprehensive systems serological profiling platform, the humoral …
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