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Faculty Detail    
Name HUBERT M. TSE
 
Campus Address SHEL 1202 Zip 2182
Phone 205-934-7037
E-mail htse@uab.edu
Other websites PubMed
     


Faculty Appointment(s)
Appointment Type Department Division Rank
Primary  Microbiology  Microbiology Assistant Professor
Center  Arthritis & Musculoskeletal Diseases Center  Arthritis & Musculoskeletal Diseases Center Assistant Professor
Center  Center for Metabolic Bone Disease  Center for Metabolic Bone Disease Assistant Professor
Center  Medicine  Comprehensive Diabetes Ctr (Org Ret) Assistant Professor

Biographical Sketch 
Virginia Tech, B.S. 1992
University of Colorado Health Sciences Center, Ph.D. 1999
Colorado State University, Post-doctoral fellow 2001
University of Pittsburgh, Post-doctoral fellow 2009

Research/Clinical Interest
Title
The role of oxidative stress on autoimmune Type 1 diabetes
Description
My research seeks to understand the synergy of oxidative stress and autoimmune destruction of insulin-secreting pancreatic beta-cells in Type 1 diabetes (T1D). Oxidative stress and the generation of free radicals are not only important effector molecules in pancreatic beta-cell death, but they also serve to enhance autoimmune responses in T1D. We have focused on dissipating free radicals as a potential target to preserve pancreatic beta-cells and to mediate immune tolerance and suppression of autoreactive T cell responses. To address the significance of free radical synthesis and T1D, we have developed unique animal models to further understand the interplay of free radicals and dysregulated autoimmune responses in T1D. In combination with the knowledge gained from our animal models, we have also initiated translational studies to characterize the efficacy of a powerful catalytic antioxidant to dissipate oxidative stress as a novel immunotherapeutic treatment for the prevention of T1D.

Selected Publications 
Publication PUBMEDID
Click URL under “Faculty Detail” above to link to current publications on PubMed   

Keywords
Autoimmunity, Type 1 diabetes, Reactive Oxygen Species, T cell, Innate Immunity, Inflammation