O Granuloma \"lepróide canino\", quadro sindrômico, também denominada lepra canina, foi descrito pela primeira vez em 1973, no Zimbábue, em cães da raça Boxer e Bull mastiff e consiste em um dos tipos de micobacterioses tegumentares encontradas nos animais de companhia. No presente estudo, objetivou-se caracterizar os aspectos clínicos e epidemiológicos da enfermidade, nos animais atendidos no período de 1990 a 2010, no Serviço de Dermatologia do Hospital Veterinário da Faculdade de Medicina Veterinária e Zootecnia da Universidade de São Paulo, bem como determinar a ocorrência de similaridade gênica da micobactéria envolvida, entre os animais brasileiros e os descritos em trabalhos estrangeiros. A amostragem foi composta de 37 animais com diagnóstico estabelecido por exame histopatológico ou citobacterioscópico cutâneo, onde se verificou evidente predisposição racial (83,7%), principalmente da raça Boxer (61,2%), ampla distribuição etária e ausência de predisposição sexual. Os cães apresentavam bom estado geral, sem comprometimento sistêmico, apenas tegumentar, com predomínio das lesões de morfologia nodular (75,6%) e situadas em pavilhões auriculares (86,5%). O diagnóstico foi estabelecido a partir dos seguintes exames subsidiários: histopatologia cutânea (56,8%), citobacterioscopia (21,6%) e por ambas as metodologias (21,6%). Trata-se ainda de enfermidade ocorrente em várias unidades federativas brasileiras, no entanto parece ser pouco diagnosticada e assim submetida a tratamentos equivocados, o que foi verificado em 54% dos cães tratados preteritamente. Os fármacos empregados no tratamento sistêmico, rifampicina ou enrofloxacina, mostraram-se igualmente eficazes, com estabelecimento da alta clínica em tempo médio de 84,1 dias. Já técnica de reação em cadeia de polimerase (PCR) foi executada a partir de cortes histológicos cutâneos, emblocados em parafina, oriundos de 13 animais, sendo que em 09 (69,2%) deles se detectou a presença de Mycobacterium cepa CLGS, pelo método da PCR em tempo real e a confirmação do agente em comum entre os casos do Brasil e de outros países. / Canine leproid granuloma, syndromic, also called \"canine leprosy, was first described in 1973 in Zimbabwe in Boxer dogs and Bull mastiff and consists of a type of soft tissue mycobacterial infections found in pets. In the present study aimed to characterize the clinical and epidemiological aspects of the disease in animals treated between 1990-2010 at the Department of Dermatology, Veterinary Hospital, Faculty of Veterinary Medicine, University of São Paulo, and to determine the occurrence of genetic similarity of mycobacteria involved, of dogs from Brazil and other countries. The sample consisted of 37 animals with diagnosis established by histopathology or cytology skin, where there was clear racial predisposition (83.7%), mainly Boxer (61.2%), broad age distribution and no sexual predisposition. The dogs were in good general condition, without systemic involvement, only cutaneous, with a predominance of nodular lesions morphology (75.6%) located in the ears (86.5%). The diagnosis was established from the following exams: cutaneous histopathology (56.8%), citology (21.6%) and by both methods (21.6%). It is still disease occurring in several Brazilian states, however appears to be underdiagnosed and thus subjected to inappropriate treatment, which was observed in 54% of dogs treated. The drugs used in systemic treatment, rifampin and enrofloxacin, were equally effective, with the establishment of recovery a mean of 84.1 days. Already technique of polymerase chain reaction (PCR) was performed from histological sections of skin, paraffin embedded, from 13 animals, while in 09 (69.2%) of them detected the presence of Mycobacterium strain CLGS by method of real-time PCR and confirmation of the agent in common between the cases of Brazil and other countries.

Les granulomes signent une réponse immune efficace dans de nombreuses maladies infectieuses. C’est le cas de la fièvre Q où ils sont présents dans la forme aiguë de la maladie spontanément résolutive mais où ils sont absents dans sa forme chronique. J’ai mis au point une méthode permettant d’étudier la formation in vitro des granulomes à partir de cellules mononucléées du sang périphérique incubées en présence de billes de Sepharose recouvertes d’extraits de C. burnetii, l’agent de la fièvre Q. Ces granulomes apparaissent en quelques jours avant de disparaître au bout d’une vingtaine de jours. Ils sont composés essentiellement de macrophages et de lymphocytes et, à un moindre degré, de cellules épithélioïdes, de cellules géantes multinucléées et de cellules dendritiques. La méthode d’obtention in vitro des granulomes a permis également d’étudier les premiers stades de leur formation grâce à la mise au point d’une technique en live imaging d’observation en lumière transmise des cellules. J’ai montré que les monocytes, les premières cellules à migrer vers les billes et à entièrement les recouvrir, initient le recrutement des lymphocytes. J’ai également montré que le défaut de formation des granulomes observés chez des patients atteints d’une fièvre Q chronique pourrait être lié à un défaut de migration de leurs monocytes circulants. / Granulomas indicate effective immune response in a large number of infectious diseases. The primo-infection by Coxiella burnetii, the agent of Q fever, is spontaneously resolutive and is characterized by the presence of granulomas, whereas granulomas are absent in the chronic form of the disease. I developed a new method to study in vitro the formation of granulomas using peripheral blood mononuclear cells incubated in the presence of Sepharose beads coated with C. burnetii extracts. Granulomas appeared in few days before disappearing at day 20. They were essentially composed of macrophages and lymphocytes and, in a lesser extent, of epithelioid cells, multinucleated giant cells and dendritic cells. The method to obtain in vitro granulomas allowed the study of the first events of granuloma formation in live imaging microscopy. Monocytes migrated toward Sepharose beads and entirely covered these beads, and initiated the recruitment of lymphocytes. Finally, mononuclear cells from patients with Q fever were unable to generate granulomas due to defective migration of monocytes. We hypothesize that defective migration of monocytes may be responsible for the defective formation of granulomas in Q fever.

Chemotherapy of tuberculosis (TB), a disease caused by Mycobacterium tuberculosis (M. tuberculosis), is successful against actively-growing bacilli but ineffective against dormant/persistent organisms, found mainly in a protective lipid-laden granuloma, possibly necessitating the use of lipophilic antibiotics. In vitro, these bacilli are encased in lipid-rich biofilms. In this study, the antimycobacterial activity of one such agent, clofazimine, and its nanoparticle formulation, have been investigated against Mycobacterium smegmatis (M. smegmatis), as a surrogate for M. tuberculosis, by determining the bacteriostatic and bactericidal activities of the native (NC) and spray-dried (SDC) preparations of this agent on planktonic and biofilm populations, as well as their effects on biofilm formation and its lipid compositions, specifically free mycolic acid (FM) content. Both preparations were comparable, being bacteriostatic for rapidly-proliferating bacilli, bactericidal for slow-growing, biofilm-producing sessile bacteria, but ineffective against non-replicating, biofilm-encased M. smegmatis organisms. However, similar studies in M. tuberculosis are required. / Dissertation (MSc)--University of Pretoria, 2013. / Immunology / Unrestricted

Periprosthetic osteolysis remains the leading complication of total hip arthroplasty. It often results in aseptic loosening of the implant with a requirement for a revision surgery. Wear-generated particular debris is the main cause of initiating this destructive process. The most important cellular target for wear debris is a macrophage, which responds to particle challenge by activatig proinflamatory signals, which contribute to increased bone resorption. The activation of the RANKL/RANK/OPG system is considered to be a likely cause of periprosthetic osteolysis leading to implant failure. The aim of this study was to examine the possible correlation between the clinical extent of osteolysis, the number of wear particles and the expression of the osteoclastic mediator RANKL in the tissues around aseptically loosened cemented and non-cemened total hip replacements. Periprosthetic tissues were harvested from 59 patients undergoing revision hip replacement for aseptic loosening. We had observed RANKL-positive cells in 23 of our 59 patients, their presence was noted predominantly in tissues with a loosened cemented endoprosthesis. We have shown that RANKL is present only in the tissues with a large amount of wear debris and predominantly in the cases involving lacunar type of osteolysis. Key words:...

INTRODUCTION: The diagnosis and treatment of endodontic infections is a multi-step fact gathering process, with the gold standard of periapical lesion diagnosis being histological biopsy. With common diagnoses, such as periapical granulomas and radicular cysts, representing the bulk of biopsies, the possibility of a less invasive method of lesion identification ought to be examined. In recent years Cone Beam Computed Tomography (CBCT) imaging has been proposed as a potential diagnostic tool for periapical diagnosis, but this theory requires further testing and data in order to verify its appropriateness. OBJECTIVE: The aim of this study was to evaluate six criteria used for assessing periapical lesions of teeth seen on CBCT scan from the textbook Oral Radiology White and Pharoah. MATERIAL AND METHODS: Three blinded endodontists observed radiographic features of oral periapical lesions of teeth previously diagnosed as either radicular cysts or periapical granulomas via histological biopsy. All lesions had previously been scanned via CBCT, and endodontic apical surgery was performed allowing for a pathology sample of the lesion. The observers viewed 40 CBCT and 40 corresponding periapical (PA) radiographic images, all randomized, and reported which of the six criteria (Location- apex of tooth, periphery- corticated border, shape- curved or circular, internal structure- radiolucent, effects on surrounding structures- displace or resorb roots, corticated plate perforation- present) were present in the scans. Data was analyzed using a Logistical Regression Fleiss Kappa statistic with a 95% confidence level. RESULTS: CBCT cyst showed no agreement between examiners criteria selected to statistical significance. The most selected criteria by all examiners were shape and internal structure. PA radiographic Cyst showed moderate agreement for ‘Location’ and ‘Periphery’ and substantial agreement on ‘none’ criteria. The most selected criteria by all examiners were internal structure and location. CBCT Granuloma showed moderate agreement for ‘location’ and perfect agreement for ‘none’. The most selected criteria by all examiners were shape, location, and internal structure. PA radiographic Granuloma showed substantial agreement for ‘periphery’ and moderate agreement for internal structure (radiolucency). The most selected criteria by all examiners were location, and occasionally shape and internal structure. Logistic regression of selected criteria shows with each additional criteria present on each lesion the chance of the lesion being a granuloma decreases 24.9% on PA radiographs and 33.9% on CBCT images. CONCLUSION: The current study shows an inter-examiner agreement of moderate to perfect kappa statistic does not align with the most commonly selected criteria among examiners, showing poor examiner agreement among lesions. / 2024-06-21T00:00:00Z

Patients with common variable immunodeficiency (CVID) are occasionally recognized to have a concurrent noncaseating granulomatous disease. The granulomatous disease (GD) associated with CVID shares many clinical properties typical of sarcoidosis. Some investigators speculate that the GD-CVID is actually sarcoidosis that is expressed atypically because of the patient's immunodeficiency. Clinical differences, however, have led other investigators to speculate that the GD-CVID is a distinct "sarcoid-like" granulomatous process.

No description available.

A tuberculose (TB) é um grave problema de saúde pública. Somente no ano de 2004, cerca de 9 milhões de pessoas desenvolveram TB ativa e mais de 2 milhões de pessoas morreram da doença. O desenvolvimento de novos modelos experimentais de TB seriam de grande utilidade para para elucidar mecanismos fisiopatológicos da doença e testar esquemas terapêuticos para a prevenção e contenção da doença. Além disso, o desenvolvimento de novas vacinas torna-se indispensável como ferramenta de prevenção e controle da TB. A TB no sistema nervoso central (SNC), assim como em outros tecidos do organismo, promove a ativação de células inflamatórias. No SNC a micróglia desempenha este papel, sendo capaz de produzir ou ser influenciada por mediadores solúveis. Vários mediadores estão envolvidos nos mecanismos moleculares decorrentes da infecção e inflamação causados pela TB, entre eles: NFB, iNOS e VEGF. A ativação do NFB, um fator de transcrição citoplasmático que sob estímulo migra para o núcleo celular, tem íntima relação com a indução da iNOS e de VEGF. A resistência intracelular a patógenos, inclusive ao Mycobacterium tuberculosis, parece estar associada a expressão de iNOS em macrófagos. O óxido nítrico (NO) tem papel importante na comunicação intercelular, estimulando a síntese de mediadores inflamatórios, como as citocinas, e regulando sua própria produção endógena. Estas citocinas por sua vez também podem induzir a atividade do NFB e a expressão da iNOS e VEGF. O VEGF é um potente ativador de permeabilidade vascular e de angiogênese, envolvido na ruptura da barreira hemato-encefálica. Neste estudo, mostramos a caracterização morfológica e imuno-histoquímica de um modelo murino de TB no SNC, com a indução da doença pela inoculação de BCG. Com este modelo experimental obtivemos importantes resultados que podem esclarecer mecanismos envolvidos na fisiopatologia da neuro-TB humana. A indução de meningite e tuberculomas foi possível através da inoculação de 104 cfu de BCG no cerebelo de camundongos, por estereotaxia, e esta indução foi dependente do tempo. A confirmação do diagnóstico foi feita pela detecção de bacilos álcool-ácido resistentes (BAAR), nas lesões tuberculosas. Observamos, ao longo do tempo (1 a 6 dias; 1, 2, 4 e 8 semanas) o recrutamento de diferentes populações gliais (micróglia e astrócitos) no sítio de injeção. Houve aumento de produção e ativação NFB nas lesões tuberculosas, caracterizada pela translocação da molécula do citoplasma para o núcleo celular. Houve expressão de iNOS restrita às lesões tuberculosas, além do aumento de expressão de VEGF nestas lesões. Além disso, camundongos imunizados com a vacina gênica hsp65, contra a TB, não expressam VEGF em suas lesões. Esta vacina parece conferir um efeito protetor em nosso modelo experimental, reduzindo a expressão de VEGF, e consequentemente reduzindo seu efeito angiogênico decorrente do processo inflamatório. O recrutamento glial, e a produção de mediadores solúveis (NFB, iNOS e VEGF) pelo hospedeiro, em resposta à invasão do patógeno no SNC, parecem estar envolvidos na fisiopatologia da neurotuberculose, como demonstrado neste modelo experimental. Nosso modelo permitirá investigar fatores possivelmente responsáveis pelo desenvolvimento e manutenção de lesões tuberculosas no SNC. O objetivo final seria elucidar a fisiopatologia desta grave doença e compreender eventos moleculares envolvidos na produção de lesões. O conhecimento gerado poderá permitir o delineamento de terapias específicas e efetivas. / Tuberculosis (TB) is a serious public health problem; in 2004, 9 million people developed active TB and the disease killed 2 million patients. Development of experimental models and new vaccines are essential both to elucidate physiopathological mechanisms and to control the disease. This infection in the central nervous system (CNS), as in other tissues of the organism, activates inflammatory cells. In CNS, this role is performed by the microglia, which is capable of producing or be influenced by soluble mediators. Several mediators are involved in the molecular mechanisms of the infection and inflammation by mycobacteria , such as NFB, iNOS and VEGF. NFB activation, a cytoplasmic transcriptional factor that migrates to the cellular nucleus under stimuli, is involved with the iNOS and VEGF induction of expression. The intracellular resistance to Mycobacterium tuberculosis has been associated with iNOS expression in macrophage cells. Nitric oxide (NO) is crucial in intercellular communication, modulating the synthesis of mediators of inflammation, such as cytokines, and modulation itself. These cytokines induces NFB activity, and induces iNOS and VEGF expression. VEGF is a potent activator of vascular permeability and of angiogenesis and it is a factor involved in the breakdown of the blood brain-barrier in tuberculous meningitis. In this study, we showed the morphologic and immunohistochemistry characterization of an experimental model of TB in the CNS, with inoculation of BCG in mice. In this model we elicited important outcome that can elucidate mechanisms involved in the physiopathology of human neuron-TB. Induction of meningitis and tuberculomas were possible with stereotaxic inoculation of 104 cfu of BCG in mice cerebellum, in a time-dependent way. Diagnostic was confirmed by detection of alcohol-acid resistant bacilli (BAAR), in tuberculous lesions. We observed, the time-course (1 to 6 days; 1, 2, 4 e 8 weeks) of the recruitment of different glial populations (microglia and astrocytes) in the injection site. There was increased production and activation of NFB in the tuberculous lesions, it was characterized by its nuclear translocation from cytoplasm. There was iNOS expression only in the tuberculous lesions, and expression increased of VEGF in these lesions. Furthermore, mice immunizated with vaccine DNA-hsp65 there was no expression of VEGF in its lesions. This vaccine seems confer a protector effect in our experimental model, reducing the expression of VEGF, and then reducing its angiogenic effect derived from inflammatory process. Glial recruitment, and the soluble mediators production (NFB, iNOS e VEGF) by the host, producing in response to invasion of the pathogen in the CNS, has been involved in the pathophysiology of the neuro-TB, such as demonstrated in this experimental model. Our model will allow investigate possible factors responsible for the development and maintenance of tuberculous lesions in the CNS. The final aim is to elucidate the physiopathology of this serious illness and understand the molecular events involved in the production of the lesions. The knowledge created may permit to pave the way to delineate specific and effective therapies.

A Doença Granulomatosa Crônica é uma imunodeficiência grave e rara, na qual os quadros infecciosos por bactérias e fungos, ocorrem predominantemente nas barreiras naturais do organismo. O defeito reside em mutações em um dos componentes do sistema NADPH oxidase. O dHPLC mostrou-se mais sensível que o SSCP, sendo eficaz na detecção de alterações em 100% dos casos. Identificamos sete mutações diferentes no gene CYBB, sendo quatro delas inéditas. São elas R226X; R290X; e C537R. Dentre as mutações inéditas identificamos: T302fsX46; c.141 +5 G> T; C185R; e H222L. Identificamos a mutação V25fsX51 no gene NCF1 em duas pacientes. Estabelecemos uma correlação entre genótipo e fenótipo clínico baseado em manifestações clínicas relevantes na DGC, nos fornecendo dados importantes de cada manifestação clínica e um índice de gravidade clínica (IGC) para cada tipo de mutação. Os resultados contribuem para a construção de estratégias que permitam a identificação dos defeitos genético-moleculares relacionados à DGC. / Chronic granulomatous disease is a primary immunodeficiency characterized by recurrent and severe infections, affecting the body barriers. In these patients, phagocytes present a failure in the respiratory burst caused by a deficiency of the NADPH oxidase system, and a microbicidal defect. Mutations affecting one of the components of the NADPH oxidase system. The dHPLC proved to be more sensitive to the SSCP, being effective in detecting changes in 100% of cases. We found seven different mutations, four of which are original. Are they R226X; R290X; and C537R. Among the unpublished mutations identified: T302fsX46; c. 141 + 5 G > T; C185R; and H222L. We identify the gene mutation V25fsX51 NCF1 in two patients. We have established a correlation between genotype and phenotype clinical relevant clinical manifestations based on DGC in providing important data from each clinical and clinical severity index (CSI) for each type of mutation. The results contribute to the construction of strategies enabling the identification of molecular genetic defects related to CGD.

Made available in DSpace on 2014-12-17T15:32:23Z (GMT). No. of bitstreams: 1 TiagoJSF_DISSERT.pdf: 3045279 bytes, checksum: 8153fafe331060792baf7be0c25c538f (MD5) Previous issue date: 2014-02-10 / Conselho Nacional de Desenvolvimento Cient?fico e Tecnol?gico / Vascular anomalies constitute a distinct group of lesions, but they may present similar clinical and histopatological characteristics, which can lead to diagnostic mistakes. This study aimed by histopathology and immunohistochemical expression of human glucose transporter protein (GLUT-1), correctly identify and classify oral vascular anomalies, besides analyzing the immunoexpression of markers proliferation and apoptosis (Ki-67 and Bcl-2). All cases diagnosed as "oral hemangiomas" belonging to the archives of the Service of Pathological Anatomy from the subject of Oral Pathology of the Department of Dentistry (DOD), of the Federal University of Rio Grande do Norte (UFRN) were reviewed, totalizing 77 cases. Immunohistochemical analysis for GLUT-1 showed that only 26 (33.8%) of the specimens were true infantile hemangiomas (IHs). The 51 (66.2%%) GLUT-1 negative specimens were then reclassified as pyogenic granulomas (PGs) and vascular malformations (VMs) from their histopathologic characteristics,totalizing 26 (33.8%) cases of IHs, 20 (26.0%) of PGs and 31 (40.2) cases of oral VMs. The cases analyzed by the marker Ki-67 showed different median IH (13,85), PG (33,70) and VM (4.55) with statistically significant differences between them (p <0.001). In relation to the protein Bcl-2, the groups also showed different median of the established scores IH (1.00), PG (1.50), VMs (0.0) demonstrating statistically significant differences between them (p<0,001). No statistically significant correlation between the indexes of positivity for Ki-67 and the scores of immunoexpression of Bcl-2 were observed in any group. Thus, we can conclude that it is necessary a careful and parameterized review of cases of vascular anomalies making use of auxiliary tools such as GLUT-1, since the histopathological findings alone, sometimes, are not sufficient to differentiate some anomalies. Furthermore, analysis of the expressions of markers involved in the levels of proliferation of lesions is important for a better understanding of its biological behavior aspect / As anomalias vasculares constituem um grupo de les?es distintas, mas que podem apresentar caracter?sticas cl?nicas e histopatol?gicas semelhantes, que podem levar a equ?vocos diagn?sticos.Este estudo objetivou por meio da histopatologia e da express?o imuno-histoqu?mica daprote?na humana transportadora de glicose (GLUT-1), identificar e classificar corretamente as anomalias vasculares orais, al?m de analisar a imunoexpress?o de marcadores de prolifera??o e apoptose (Ki-67 e Bcl-2).Todos os casos diagnosticados como hemangiomas orais pertencentes aos arquivos do Servi?o de Anatomia Patol?gica da disciplina de Patologia Oral do Departamento de Odontologia (DOD) da Universidade Federal do Rio Grande do Norte (UFRN) foram revisados, totalizando 77 casos. A an?lise imuno-histoqu?mica para GLUT-1 revelou que apenas 26 (33,8%) dos esp?cimes tratavam-se de hemangiomas da inf?ncia (HIs) verdadeiros. Os 51 (66,2%%)esp?cimes GLUT-1 negativos foram ent?o reclassificados em granulomas piog?nicos (GPs) e malforma??es vasculares (MVs) a partir de suas caracter?sticas histopatol?gicas, totalizando 26 (33,8%) casos de HIs, 20 (26,0%) de GPs e 31 (40,2) casos de MVs orais. Os casos submetidos ? an?lise do marcador Ki-67 apresentaram medianas diferentes HI (13,85), GP (33,70) e MV (4,55) com diferen?as estatisticamente significantes entre elas (p<0,001). Em rela??o ? prote?na Bcl-2, os grupos tamb?m apresentaram diferentes medianas dos escores estabelecidos HI (1,00), GP (1,50), MVs (0,0), demonstrando diferen?as estatisticamente significantes entre elas (p<0,001). N?o foi observada correla??o estatisticamente significante entre os ?ndices de positividade para o Ki-67 e os escores de imunoexpress?o de Bcl-2 em nenhum grupo.Dessa maneira, podemos concluir que se faz necess?rio uma revis?o criteriosa e parametrizada dos casos de anomalias vasculares utilizando ferramentas auxiliares, como a GLUT-1, uma vez que os achados histopatol?gicos sozinhos, ?s vezes, n?o s?o suficientes para diferenciar algumas anomalias. Al?m disso, a an?lise das express?es de marcadores envolvidos nos n?veis de prolifera??o das les?es ? um aspecto importante para o melhor entendimento do seu comportamento biol?gico