
Infection with Plasmodium spps, the parasite responsible for malaria, is currently a global health crisis. Approximately 50% of the world's population lives in malaria-endemic regions, and ~1 million people die from malaria annually. While anti-malarial drugs have been effective at treating infected individuals, drug-resistance is a common problem and they do not prevent re-infection. Alternatively, an efficacious vaccine for malaria has the potential to prevent infection and lead towards the eradication of this parasite.Given the need for a malaria vaccine, my laboratory is interested in understanding both CD8 T cell and antibody responses to Plasmodium spps. Specifically, we use the murine model of malaria to determine 1) why protective immunity fails to develop following infection with Plasmodium and 2) the magnitude of Plasmodium-specific antibodies and liver stage-specific CD8 T cell responses that are required to prevent the parasite from progressing from the asymptomatic liver stage to the clinically symptomatic blood stage. Importantly, this information will aid in the rational design of a much-needed malaria vaccine.
B.S., 2001, Olivet Nazarene University
Ph.D., 2005, Indiana University
Postdoctoral Fellow, 2006-2011, University of Iowa
M409 Walters Life Sciences
Knoxville, Tennessee 37996-0845
Phone: 865-974-6229
Fax: 865-974-4007
Email: nschmid2@utk.edu
Knoxville, Tennessee 37996 | 865-974-1000
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