Tongalp H. Tezel, M.D.
Associate Professor
of Ophthalmology
Kentucky Lions Endowed Chair
Department of Ophthalmology and Visual Sciences
Director of Fellowship
Program in Vitreoretinal
Diseases and Surgery
Surgical and medical treatment of vitreoretinal diseases and uveitis, including Age-Related Macular Degeneration, Retinal Detachment, Diabetic Retinopathy, Proliferative Vitreoretinopathy, Macular Holes and Hereditary Retinal Degenerations
301 E. Muhammad Ali Boulevard, Louisville KY 40202
Telephone: 502-852-5466 Fax: 502-852-3811
E-mail: Tongalp.Tezel@louisville.edu
Hacettepe University Medical School, Ankara, Turkey – 1984
Washington University School of Medicine, St. Louis, Missouri - 1999-2002
Clinical Fellowship in Vitreoretinal Surgery 1 - Department of Ophthalmology, Rigshospitalet Copenhagen University School of Medicine, Copenhagen, Denmark,1993-1994;
Clinical Fellowship in Vitreoretinal Surgery 2 - College of Physicians and Surgeons of Columbia University, Department of Ophthalmology, New York, NY, 2002-2003;
Fellowship in Vitreoretinal Research - Washington University School of Medicine, St. Louis, Missouri, 1994-1997
American Board of Ophthalmology, 2003
I am a clinician-scientist who has been listed as one of the “Best Doctors in America” for many consecutive years. I have been involved extensively in clinical research as well as basic science research. I have participated in several multicenter prospective drug trials, such as PIER and VIEW 1 as a principal investigator. My main clinical research focus has been to develop novel preventive and treatment strategies for blinding vitreoretinal disorders, such as age-related macular degeneration, diabetic retinopathy and retinal detachment. I developed techniques for tissue harvest, storage and delivery which allowed initial human retinal cell transplantation studies to be performed. My subsequent research laid down the groundwork for the early tissue engineering studies for rejuvenating the damaged retina as a treatment for age-related macular degeneration and various retinal dystrophies.
I also discovered the use of the enzyme Dispase for inducing pharmacological vitreolysis. This non-invasive method for separating the vitreous gel from the retina can eliminate the need of surgery for several vitreoretinal diseases, including macular holes, vitreomacular traction syndromes and diabetic eye disease.
I have been working extensively on the biological effects of anti-VEGF drugs, such as Avastin® (bevacizumab) and Lucentis® (ranibizumab). I was the first to demonstrate that these drugs can exert similar biological effects in the fellow eye. Because of this observation I cautioned the ophthalmic community about the possible systemic side effects of VEGF-blockage. Along with one of my colleagues, I was also the first demonstrate the tachyphylaxis against anti-VEGF drugs and the beneficial effects of vitrectomy in avoiding the development and progression of age-related macular degeneration.
My basic science work on proteomic and genomic analysis allowed me to identify new therapeutic targets and possible biomarkers to diagnose and monitor the age-related macular degeneration, as well as to identify patients that will benefit from treatment with anti-VEGF agents. I also employ bioengineering techniques to improve the design and function of surgical instruments.