
معرفی
Dr. Keke Fairfax serves as an Associate Professor in the Department of Microbiology and Immunology at the University of Utah, specializing in immunological responses to parasitic infections with Schistosoma mansoni as a primary model. Her work centers on IL-4-mediated immuno-modulation and the development of adaptive immune memory in contexts of maternal infection and metabolic disease.
Education:
- Bachelor of Arts (B.A.) from the University of Chicago
- Doctor of Philosophy (Ph.D.) from Yale University
Dr. Fairfax's research program investigates three interconnected themes: immunological consequences of maternal schistosomiasis on offspring immunity, IL-4's role in lymph node cellular dynamics during homeostasis and antigen challenge, and hepatic macrophage mechanisms in helminth-induced metabolic protection. Her approach integrates cellular immunology with parasitology to dissect B-T-stromal cell interactions in protective immunity.
Publication analysis reveals consistent focus on liver immunology and macrophage function within schistosomiasis research, with recurring exploration of B cell compartmentalization, IL-4/IL-10 signaling pathways, and cross-disciplinary links to metabolic disorders and pulmonary complications. Her work demonstrates strong translational potential for inflammatory disease and vaccine development.
Scientific Awards: No specific awards or fellowships are documented in the provided materials.
Dr. Fairfax mentors graduate students and postdoctoral researchers through her active laboratory, supported by federal grants typical for immunology/parasitology research. She maintains collaborative networks across immunology and infectious disease disciplines at the University of Utah and nationally, with research infrastructure including core facility access and specialized mouse infection models.
Her laboratory operations focus on the three primary research projects using Schistosoma mansoni models, employing flow cytometry, transcriptional profiling, and in vivo challenge systems to investigate immune memory mechanisms and metabolic cross-talk.




