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Rebecca Markovitz

Current Status: GRAD

Graduate Department: Immunology and Molecular Pathogenesis

Other Degrees: History, Yale University;  

Advisor(s): Pete Lollar, MD;

Hometown: Ann Arbor, MI

Hobbies

Reading, Running, Socializing, and Baking

Research

The standard of care for patients with congenital hemophilia A is the infusion of recombinant or plasma-derived factor VIII (fVIII). Approximately 30% of patients develop detectable inhibitory anti-fVIII antibodies (inhibitors) in response to these infusions, which is the most serious complication in the treatment of hemophilia A. In addition, non-hemophiliacs can break tolerance to their native fVIII protein. We have characterized the diversity of the immune response against fVIII using a murine hemophilia A model and are presently focusing on preventing the development  of the inhibitors.

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