Doctor of Philosophy / Profound perturbation of epithelial structure is a characteristic feature of the immunopatholoical response to bacterial antigens considered to be central in the pathogenesis of the destructive lesion of periodontitis. The pathological basis for the disturbance of epithelial structure is not understood. It was demonstrated that the structural integrity and functional differentiation of the lining epithelium is compromised in relation to inflammatory changes associated with destructive periodontitis. In the pathological lining epithelium of the periodontal pocket there was a marked reduction of epithelial cadherin important in intercellular adhesion, of involucrin, a marker of terminal differentiation, and of the gap junction connexions that form intercellular communication channels. These changes were associated with alterations of filamentous actin expression, collectively indicating profound perturbation of epithelial structure. The data reported support the concept that the ability of the pathological lining epithelium to function as an effective barrier against the ingress of microbial products into the tissues is severely compromised (Ye et al., 2000). In addition, a recent study (Ye et al., 2003) by Western analysis of serum IgG from all 22 patients with chronic periodontitis tested indicated recognition of multiple epithelial components in individual patterns. In contrast, subjects with a healthy periodontium displayed only trace recognition of epithelial antigens. Levels of epithelial-reactive antibodies were significantly correlated with attachment loss as an indication of disease activity. To investigate a possible relationship between the bacterial flora adjacent to the diseased sites and the presence of epithelial-reactive antibodies, subgingival plague samples were taken from deep periodontal pockets and cultured anaerobically. Gram positive bacteria containing antigens potentially cross-reactive with epithelial cells were reproducibly isolated by probing membrane colony lifts with affinity-isolated (epitheial-specific) antibodies. The bacteria were identified as streptococci (S. mitis, S. constellatus and two S. intermedius strains) and Actinomyces (A. georgiae, and A. sp. oral clone) by 16S rDNA sequence homology. Recognition by affinity-isolated antibodies of antigens from the captured organisms was confirmed by Western analysis. Conversely, absorption of affinity-isolated antibodies with bacterial species specifically reduced subsequent recognition of epithelial antigens. To identify the auto-antigens, a human keratinocyte cDNA expression library in Lambda phage was probed using a pooled sera. Groups of responders were detected for CD24 (a recently described adhesion molecule also known as P-selectin ligand), antioxidant protein 2 (a newly recognised member of the thiol-dependment anti-oxidant proteins), lavtate dehydrogenase A, the transcription factor NFAT5, and for three genes encoding novel proteins. Six identified bacteria, especially S intermedius were demonstrated to absorb antibodies reaching with identified auto-antigens in patterns varying between individuals. This evidence indicated that during the course of periodontits, subjects develop increased levels of antibodies to common oral bacteria amongst which are included tissue cross-reactive antigens. Periodontitis could therefore present a risk for the subsequent initiation or exacerbation of a broad spectrum of disease processes including autoimmune, inflammatory, proliferative and degenerative disorders.

Das parodontopathogene Bakterium Aggregatibacter actinomycetemcomitans (A. actinomycetemcomitans) exprimiert zahlreiche Virulenzfaktoren. In dieser Studie wurden die Gene für die Virulenzfaktoren Leukotoxin (LtxA), Cytolethal Distending Toxin (CDT) und Fimbriae-assoziiertes Protein (Flp1) in 99 A. actinomycetemcomitans-Isolaten aus der Plaque von Parodontitispatienten aus vier deutschen Universitätskliniken untersucht. Die Proben wurden serotypisiert. Die Entnahme erfolgte mit sterilen Papierspitzen aus der jeweils tiefsten Tasche jedes Quadranten. Es wurden von den Patienten Sondierungstiefe (PD) und Attachmentlevel (AL) an sechs Stellen pro Zahn gemessen und ebenfalls die Tiefen an den vier Entnahmestellen notiert. Außerdem wurden ethnische Herkunft der Eltern, Geschlecht und Raucherstatus erfragt. Lediglich zwei A. actinomycetemcomitans-Isolate aus Frankfurt/Main wiesen das ltx-Gen mit Deletion auf. Diese zeigten signifikant höhere PD an den vier Entnahmestellen. Die übrigen 97 Proben hatten das ltx-Gen ohne Deletion in der DNA-Promotorregion ihrer A. actinomycetemcomitans-Stämme. Probanden mit Genlokus für das cdtB-Gen, mit drei cdt-Genen oder insgesamt fünf Genen für Virulenzfaktoren litten signifikant häufiger an aggressiver Parodontitis. A. actinomycetemcomitans-Isolate mit cdtA-Gen, cdtB-Gen, cdtCGen, drei cdt-Gene oder flp-1-Gen wiesen signifikant häufiger Serotyp b oder c auf. Probanden ohne cdtC-Gen oder flp-1-Gen in der DNA ihrer isolierten A. actinomycetemcomitans-Stämme zeigten am häufigsten Serotyp e. Probanden mit Genlokus für das cdtB-Gen oder drei cdt-Gene in den isolierten A. actinomycetemcomitans-Proben oder mit aggressiver Parodontitis stammten signifikant häufiger aus dem Ausland. Es wurde kein signifikanter Zusammenhang zwischen Vorkommen der Gene für Virulenzfaktoren und PD bzw. AL im gesamten Gebiss gefunden.

Este estudio se efectuó con el propósito de conocer el nivel de resorción ósea alveolar en las personas diabéticas causado por periodontitis crónica, en comparación con un grupo control, en nuestro medio. Para ello se examinaron todas las piezas dentarias presentes en 20 pacientes diabéticos pertenecientes al Programa de Diabetes del Servicio de Endocrinología del Hospital Nacional Arzobispo Loayza e igual número de pacientes no diabéticos de la Clínica de la Facultad de Odontología de la Universidad Nacional Mayor de San Marcos. Se tomaron radiografías periapicales utilizando la técnica de la bisectriz del ángulo de todas las piezas dentarias que mostraron una pérdida de adherencia clínica mayor o igual a 4 mm. (piezas con periodontitis moderada y severa) para luego medir la resorción ósea alveolar tanto en mesial y distal. Todos los pacientes examinados fueron del sexo femenino, comprendidos entre 45 y 60 años. Los resultados de la investigación revelan que: No existe diferencia significativa en la cantidad de piezas dentarias con presencia de resorción ósea alveolar entre el grupo de estudio (diabéticos tipo 2) y el grupo control (no diabéticos). Existe diferencia en el grado de enfermedad periodontal, representado por la resorción de hueso alveolar, entre el grupo de estudio (diabéticos tipo 2) = 4.81 mm. promedio y el grupo control (no diabéticos) = 2.69 mm. promedio / This study was done to know the level of the alveolar bone reabsorption in diabetic people causado by cronic periodontitis, comparated with a control group in our population. For this purpose, all teeth presents in 20 diabetics patients that belong to the Diabetes Program of the Endocrinology Service of Arzobispo Loayza Hospital and a similar number of non diabetics patients of the Dentistry School of San Marcos University were examinated. Periapical radiographies were taken with the bisector of the angle technic to all the teeth that had clinic atachment lost of 4 or more mm. (teeth with moderate and severe periodontitis) in order to measure the alveolar bone reabsorption in mesial and distal. All patients examinated were female between 45 and 60 years old. The results of this research were: There is no significant difference in the cuantity of teeth with alveolar bone reabsorption between the study group (type 2 diabetics) and the control group (non diabetics). Exist difference in the severity of periodontal disease, representated by the alveolar bone resorción between the study group (type 2 diabetics) = 4.81 mm promedy and the control group (non diabetics) = 2.69 mm promedy

published_or_final_version / Dentistry / Master / Master of Dental Surgery

Genetic and epigenetic factors that predispose to ineffective control of subgingival biofilm composition are incompletely understood. The objective of this study was to elucidate how leukocytes impact on the course of periodontitis in Rac-null mice. Models of acute gingivitis and periodontitis were used to assess the early inflammatory response and patterns of chronicity leading to alveolar bone loss. Leukocyte margination was differentially impaired during attachment in conditional Rac1-null and during rolling and attachment in Rac2-null mice. The inflammatory responses to subgingival ligatures were altered in Rac-null compared to WT mice. In response to persistent subgingival challenge Rac-null mice had increased alveolar bone loss with resorption patterns characteristic to aggressive periodontitis, partially explained by higher osteoclastic activity in Rac-null mice. This study demonstrates that migratory leukocyte defects are rate limiting steps in the periodontal inflammatory process that lead to more aggressive forms of periodontitis.

Genetic and epigenetic factors that predispose to ineffective control of subgingival biofilm composition are incompletely understood. The objective of this study was to elucidate how leukocytes impact on the course of periodontitis in Rac-null mice. Models of acute gingivitis and periodontitis were used to assess the early inflammatory response and patterns of chronicity leading to alveolar bone loss. Leukocyte margination was differentially impaired during attachment in conditional Rac1-null and during rolling and attachment in Rac2-null mice. The inflammatory responses to subgingival ligatures were altered in Rac-null compared to WT mice. In response to persistent subgingival challenge Rac-null mice had increased alveolar bone loss with resorption patterns characteristic to aggressive periodontitis, partially explained by higher osteoclastic activity in Rac-null mice. This study demonstrates that migratory leukocyte defects are rate limiting steps in the periodontal inflammatory process that lead to more aggressive forms of periodontitis.

Doctor of Philosophy / Profound perturbation of epithelial structure is a characteristic feature of the immunopatholoical response to bacterial antigens considered to be central in the pathogenesis of the destructive lesion of periodontitis. The pathological basis for the disturbance of epithelial structure is not understood. It was demonstrated that the structural integrity and functional differentiation of the lining epithelium is compromised in relation to inflammatory changes associated with destructive periodontitis. In the pathological lining epithelium of the periodontal pocket there was a marked reduction of epithelial cadherin important in intercellular adhesion, of involucrin, a marker of terminal differentiation, and of the gap junction connexions that form intercellular communication channels. These changes were associated with alterations of filamentous actin expression, collectively indicating profound perturbation of epithelial structure. The data reported support the concept that the ability of the pathological lining epithelium to function as an effective barrier against the ingress of microbial products into the tissues is severely compromised (Ye et al., 2000). In addition, a recent study (Ye et al., 2003) by Western analysis of serum IgG from all 22 patients with chronic periodontitis tested indicated recognition of multiple epithelial components in individual patterns. In contrast, subjects with a healthy periodontium displayed only trace recognition of epithelial antigens. Levels of epithelial-reactive antibodies were significantly correlated with attachment loss as an indication of disease activity. To investigate a possible relationship between the bacterial flora adjacent to the diseased sites and the presence of epithelial-reactive antibodies, subgingival plague samples were taken from deep periodontal pockets and cultured anaerobically. Gram positive bacteria containing antigens potentially cross-reactive with epithelial cells were reproducibly isolated by probing membrane colony lifts with affinity-isolated (epitheial-specific) antibodies. The bacteria were identified as streptococci (S. mitis, S. constellatus and two S. intermedius strains) and Actinomyces (A. georgiae, and A. sp. oral clone) by 16S rDNA sequence homology. Recognition by affinity-isolated antibodies of antigens from the captured organisms was confirmed by Western analysis. Conversely, absorption of affinity-isolated antibodies with bacterial species specifically reduced subsequent recognition of epithelial antigens. To identify the auto-antigens, a human keratinocyte cDNA expression library in Lambda phage was probed using a pooled sera. Groups of responders were detected for CD24 (a recently described adhesion molecule also known as P-selectin ligand), antioxidant protein 2 (a newly recognised member of the thiol-dependment anti-oxidant proteins), lavtate dehydrogenase A, the transcription factor NFAT5, and for three genes encoding novel proteins. Six identified bacteria, especially S intermedius were demonstrated to absorb antibodies reaching with identified auto-antigens in patterns varying between individuals. This evidence indicated that during the course of periodontits, subjects develop increased levels of antibodies to common oral bacteria amongst which are included tissue cross-reactive antigens. Periodontitis could therefore present a risk for the subsequent initiation or exacerbation of a broad spectrum of disease processes including autoimmune, inflammatory, proliferative and degenerative disorders.

Diss. (sammanfattning) Stockholm : Karol. inst. / Härtill 7 uppsatser.

Thesis (M.S.)--University of Michigan, 1978.

Thesis (Ph. D.)--University of Washington, 1998. / Vita. Includes bibliographical references (leaves [110]-127).