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Guba wins student AADR award

Published: March 29th, 2012

Category: Honors, Awards & Appointments, News, Research

Nina Guba

Nina Guba, a D.M.D. student in the class of 2015, won second place in the 2012 Student Research Group DENTSPLY/Caulk competition in the clinical science category during the American Association of Dental Researchers Annual Meeting in Tampa, Fla., March 21 – 24.
 
The competition was held on March 21. Guba was one of 14 dental students from across the United States selected to give a ten-minute presentation to a student panel of judges. Three winners were selected in two categories, basic and clinical science, and were recognized during the annual meeting’s closing ceremonies. As a second-place winner, Guba received $500 each and a commemorative plaque.

Nina Guba wins student AADR award

from left: Shannon Wallet, Ph.D.; Guba; Luciana Shaddox, D.D.S., M.S., Ph.D.; Robert Burne, Ph.D.; and Teresa A. Dolan, D.D.S., M.P.H.

Guba’s presentation, “Inflammatory response of Aggressive Periodontitis upon Stimulation of toll-like receptors,” discussed her work comparing the inflammatory response of patients with localized aggressive periodontitis (LAP) to the response of their healthy siblings and controls when toll-like receptors were stimulated. LAP is a severe, rapidly progressive form of periodontal disease that can result in tooth loss. 

Abstract
Inflammatory response of Aggressive Periodontitis upon Stimulation of toll-like receptors
N. GUBA1, H. HUANG2, I. AUKHIL2, S. WALLET3, and L. SHADDOX3, 1University of Florida, Gainesville, FL, 2Periodontology, University of Florida, Gainesville, FL, 3Periodontology and Oral Biology, University of Florida, Gainesville, FL

Background: Localized aggressive periodontitis (LAP) is a severe rapidly progressive form of periodontal disease, localized to incisors and first molars of, usually, young individuals, and can result in eventual tooth loss. The inflammatory process of the disease is attributed to recognition of bacterial components by Toll-like receptors (TLRs) in epithelial cells. Previous research has shown that a hyper-inflammatory phenotype is concomitant with LAP patients upon stimulation of TLR2 and TLR4.

Objective: To compare the inflammatory response of LAP patients with healthy siblings and controls upon stimulation of TLR 2, TLR 4, TLR1/2, TLR 5, TLR2/6.

Methods: Whole peripheral blood samples were collected from a cohort of African-American adolescents aged 7-20 years. This included 9 patients diagnosed with LAP, 8 healthy siblings of LAP patients, and 7 healthy unrelated controls. Whole blood was stimulated with the appropriate ligand for each TLR and incubated for 24 hours. Unstimulated blood served as a negative control. A Luminex assay was used to measure the levels of 14 different chemo/cytokines and analyzed using Milliplex software. Kruskal-Wallis ANOVA with Dunn’s multiple comparisons were used for comparisons among experimental groups for each cytokine.

Results: A hyper-response was found for LAP patients upon different TLRs, especially TLR2 stimulations for different cytokines. Overall, LAP exhibited a more robust cytokine response than either healthy control group, and healthy siblings exhibited slightly higher levels of certain cytokines than unrelated healthy controls.

Conclusion: This study suggests that stimulation of different TLRs, especially TLR2, elicits a unique cytokine profile that is more robust in LAP patients. This hyper-inflammatory response is thought to contribute the severe nature of the disease.