Home About Press Employ Contact Spyglass Advanced Search
HHMI Logo
HHMI News
HHMI News
Scientists & Research
Scientists & Research
Janelia Farm
Janelia Farm
Grants & Fellowships
Grants & Fellowships
Resources
Resources
  Scientists & Research
  Overview  
dashed line
  FindSci  
dashed line
Scientific Competitions
dashed line
Investigators
dashed line
  JFRC Scientists  
dashed line
  International Research Scholars  
dashed line
  Professors  
dashed line
  Nobel Laureates  

HHMI-NIH Research Scholars
Learn about the HHMI-NIH Research Scholars Program, also known as the Cloister Program. Moresmall arrow

dashed line

Janelia Farm Research Campus
Learn about the new HHMI research campus located in Virginia. Moresmall arrow

International Research Scholars
Prime-Boost Immunization Against Malaria


Summary: Dr. Hill is working on the development of a vaccine against malaria.

A large variety of approaches to developing an effective malaria vaccine are under investigation worldwide. Pre-erythrocytic vaccines have recently shown particular promise. A protein-adjuvant vaccine encoding the circumsporozoite protein RTS,S/AS02 has shown substantial but short-term efficacy in a Gambian field trial. Heterologous prime-boost immunization focuses on maximizing effector T cell responses against the liver-stage parasite. In animal models of malaria, we have found prime-boost immunization using two viral vectors (fowlpox-MVA or adenovirus-MVA) to be more immunogenic and protective than DNA-MVA regimes.

In a series of Phase I and IIa clinical trials of this approach, three different candidate malaria vaccines (plasmid DNA, modified vaccinia virus Ankara [MVA], and fowlpox strain 9) have been administered in various combinations to more than 400 individuals in Oxford, The Gambia, and Kenya. The vaccines each encode either a polyepitope string fused to the whole Plasmodium falciparum TRAP antigen or the entire circumsporozoite antigen. When delivered with MVA as the boosting vaccine, heterologous prime-boost immunization regimes with these vaccines induced exceptionally high frequencies of interferon-gamma (IFN-gamma)–secreting antigen-specific CD4+ and CD8+ T cell responses. Responses declined over time but were re-boostable at one year with a single MVA immunization. These vaccination regimens have been safe and well tolerated without any serious adverse vaccine-related events. Vaccination induced repeatable partial and complete protection against heterologous strain sporozoite challenge in some volunteers, with the best regimes inducing on average a greater than 85 percent reduction in liver parasite burden. Further potential improvements to this vaccination approach, using a six-antigen polyprotein as an insert, and antibody-inducing and blood-stage antigen components are under development. DNA-based vaccines used in prime-boost regimes are safe and immunogenic and have repeatable quantifiable efficacy against malaria in humans.

INTERNATIONAL RESEARCH SCHOLAR

Adrian Vivian S. Hill
Adrian Vivian S. Hill
 

Related Links

AT HHMI

bullet icon

The Worldwide War on Malaria

bullet icon

HHMI International Program

dashed line
 Back to Topto the top
HHMI Logo

Home | About HHMI | Press Room | Employment | Contact

© 2008 Howard Hughes Medical Institute. A philanthropy serving society through biomedical research and science education.
4000 Jones Bridge Road, Chevy Chase, MD 20815-6789 | (301) 215-8500 | e-mail: webmaster@hhmi.org