Made available in DSpace on 2014-06-11T19:29:34Z (GMT). No. of bitstreams: 0 Previous issue date: 2009-09-02Bitstream added on 2014-06-13T19:38:45Z : No. of bitstreams: 1 carvalho_sm_me_botfm.pdf: 851185 bytes, checksum: eea10cd209e9c4f24efd8d9bd0d1f8fb (MD5) / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) / A febre reumática (FR) é uma doença pós-infecciosa, causada pelo Streptococus β hemolítico do Grupo A de Lancefield, de mecanismo auto-imune. As suas manifestações clínicas principais são denominadas sinais maiores, incluindo a artrite, cardite, coréia, nódulos subcutâneos e eritema marginado. Entre as manifestações denominadas sinais menores estão o aumento do intervalo P-R no eletrocardiograma, febre, provas de fase aguda positivas, como a VHS e a proteína C reativa. A comprovação de infecção recente pelo estreptococo é considerada um critério essencial. A FR é ainda prevalente nos países em desenvolvimento e emergentes, tendo como complicações crônica o dano valvular causado pela cardite. A sua prevenção é realizada com a erradicação do estreptococo na orofaringe, por meio da profilaxia primária com penicilina benzatina e a profilaxia secundária com a manutenção da penicilina benzatina em intervalos de 21 dias, de acordo com a recomendação da OMS. Como a FR pode apresentar seqüelas, impacto social e na qualidade de vida, justifica-se a avaliação do desfecho clínico e as suas manifestações em longo prazo. Examinar a epidemiologia, as características clínicas e o desfecho da FR em uma série de casos, nos últimos 20 anos em uma unidade acadêmica dedicada à reumatologia pediátrica (HC-FMB-UNESP). 178 casos foram identificados no período de 1986 a 2007 e destes, 134 foram revisados de acordo com um protocolo listando as manifestações clínicas e laboratoriais, o uso de medicação, o período de acompanhamento e os episódios de recorrência durante o seguimento para vigilância da profilaxia secundária. Os dados demográficos, assim como as manifestações clínicas, laboratoriais e de desfecho são apresentados por meio de freqüência para os dados categóricos e pela estatística descritiva para variáveis contínuas. A probabilidade... / Rheumatic Fever (RF) is a post-infectious disease caused by group A Streptococcus, with autoimmune mechanism. The main clinical features are named major signs as arthritis, carditis, chorea, subcutaneous nodules and erythema marginatum. Among other features, there are the minor signs as increased P-R interval on electrocardiogram (ECG), fever and acute phase reaction measured by erythrocyte sedimentation rate (ESR) or C-reactive protein (CRP). Evidence of previous streptococcal infection is considered a core criteria. RF is highly prevalent in developing countries, where the main complication is damaged heart valves due to carditis. Prophylaxis is called primary when long-acting benzyl penicilin is administered for the first time after diagnosis and it is called secondary prophylaxis for maintenance treatment with long-acting benzyl penicilin every 3 weeks, according to the WHO guidelines. As RF may result in heart damage with both quality of life and social impact, it is valuable to assess its long term outcome. To examine epidemiology , clinical features and outcome of RF in a paediatric case series, seen in an academic unit dedicated to paediatric rheumatology (HC-FMB-UNESP) during the last 20 years. 178 cases were identified from 1986 to 2007, of those 134 were fully revised according to a standardized protocol checking for clinical and laboratorial features, treatment, follow up and acute RF relapse during follow up for prophylaxis surveillance. Demographics, clinical and laboratorial features as well as outcome data are reported by frequency for categorical variables. Continuous variables are presented by descriptive statistics. The probability of carditis, valve damage and RF relapses were examined by survival analysis with actuarial survival plots. Of 134 revised cases, age at onset was from 4 to 13.8 years, follow up duration was from 1.1 to 16.9 years mean 6.8 SD (3.6) and median... (Complete abstract click electronic access below)

Orientador: Claudia Saad Magalhães / Banca: Sáskia Maria Wiegerinck Fekete / Banca: Maria Odete Esteves Hilário / Resumo: A febre reumática (FR) é uma doença pós-infecciosa, causada pelo Streptococus β hemolítico do Grupo A de Lancefield, de mecanismo auto-imune. As suas manifestações clínicas principais são denominadas sinais maiores, incluindo a artrite, cardite, coréia, nódulos subcutâneos e eritema marginado. Entre as manifestações denominadas sinais menores estão o aumento do intervalo P-R no eletrocardiograma, febre, provas de fase aguda positivas, como a VHS e a proteína C reativa. A comprovação de infecção recente pelo estreptococo é considerada um critério essencial. A FR é ainda prevalente nos países em desenvolvimento e emergentes, tendo como complicações crônica o dano valvular causado pela cardite. A sua prevenção é realizada com a erradicação do estreptococo na orofaringe, por meio da profilaxia primária com penicilina benzatina e a profilaxia secundária com a manutenção da penicilina benzatina em intervalos de 21 dias, de acordo com a recomendação da OMS. Como a FR pode apresentar seqüelas, impacto social e na qualidade de vida, justifica-se a avaliação do desfecho clínico e as suas manifestações em longo prazo. Examinar a epidemiologia, as características clínicas e o desfecho da FR em uma série de casos, nos últimos 20 anos em uma unidade acadêmica dedicada à reumatologia pediátrica (HC-FMB-UNESP). 178 casos foram identificados no período de 1986 a 2007 e destes, 134 foram revisados de acordo com um protocolo listando as manifestações clínicas e laboratoriais, o uso de medicação, o período de acompanhamento e os episódios de recorrência durante o seguimento para vigilância da profilaxia secundária. Os dados demográficos, assim como as manifestações clínicas, laboratoriais e de desfecho são apresentados por meio de freqüência para os dados categóricos e pela estatística descritiva para variáveis contínuas. A probabilidade... (Resumo completo, clicar acesso eletrônico abaixo) / Abstract: Rheumatic Fever (RF) is a post-infectious disease caused by group A Streptococcus, with autoimmune mechanism. The main clinical features are named major signs as arthritis, carditis, chorea, subcutaneous nodules and erythema marginatum. Among other features, there are the minor signs as increased P-R interval on electrocardiogram (ECG), fever and acute phase reaction measured by erythrocyte sedimentation rate (ESR) or C-reactive protein (CRP). Evidence of previous streptococcal infection is considered a core criteria. RF is highly prevalent in developing countries, where the main complication is damaged heart valves due to carditis. Prophylaxis is called primary when long-acting benzyl penicilin is administered for the first time after diagnosis and it is called secondary prophylaxis for maintenance treatment with long-acting benzyl penicilin every 3 weeks, according to the WHO guidelines. As RF may result in heart damage with both quality of life and social impact, it is valuable to assess its long term outcome. To examine epidemiology , clinical features and outcome of RF in a paediatric case series, seen in an academic unit dedicated to paediatric rheumatology (HC-FMB-UNESP) during the last 20 years. 178 cases were identified from 1986 to 2007, of those 134 were fully revised according to a standardized protocol checking for clinical and laboratorial features, treatment, follow up and acute RF relapse during follow up for prophylaxis surveillance. Demographics, clinical and laboratorial features as well as outcome data are reported by frequency for categorical variables. Continuous variables are presented by descriptive statistics. The probability of carditis, valve damage and RF relapses were examined by survival analysis with actuarial survival plots. Of 134 revised cases, age at onset was from 4 to 13.8 years, follow up duration was from 1.1 to 16.9 years mean 6.8 SD (3.6) and median... (Complete abstract click electronic access below) / Mestre

The Lyme disease spirochete Borrelia burgdorferi is the only known human pathogen that directly activates invariant natural killer T (iNKT) cells. The number and activation kinetics of iNKT cells vary greatly among different strains of mice. Here, we report the role of the iNKT cell response in the pathogenesis of Lyme disease using C57BL/6 (B6) mice, a strain with optimal iNKT cell activation that is resistant to the development of spirochetal-induced inflammation. During experimental infection of B6 mice with B. burgdorferi , iNKT cells localize to the inflamed heart where they are activated by CD1d-expressing macrophages. Activation of iNKT cells in vivo results in the production of IFNγ, which we demonstrate controls the severity of murine Lyme carditis by at least two mechanisms. First, IFNγ greatly enhances the recognition of B. burgdorferi by macrophages, leading to increased phagocytosis of the spirochete. Secondly, IFNγ activation of macrophages increases the surface expression of CD1d, thereby facilitating further iNKT activation. Collectively, our data demonstrate that in the resistant background, B6, iNKT cells modulate acute murine Lyme carditis through the action of IFNγ, which appears to self-renew through a positive feedback loop during infection. Inflammation during infection with B. burgdorferi is dependent on the ability of the spirochete to evade local mechanisms of clearance. Even though macrophages are the main infiltrating cell during Lyme carditis, the identification of a receptor capable of mediating phagocytosis of B. burgdorferi has been elusive. Here, we demonstrate that the integrin CR3 is able to mediate binding to the spirochete and facilitate phagocytosis in a complement-dependent and independent manner. Expression of CR3, but not CR4, in CHO cells markedly enhanced their capacity to interact with B. burgdorferi , in the absence and presence of complement opsonization. Furthermore, the interaction between CR3 and B. burgdorferi is dependent on the metal-ion-dependent adhesion site (MIDAS) and could be blocked with EDTA. Inhibition of CR3 with blocking antibody was able to completely abrogate phagocytosis of B. burgdorferi by the macrophage-like RAW264.7 cells and partially block uptake by bone marrow-derived macrophages (BMMs), a finding that was recapitulated with CD11b-deficient BMMs. We further show that activation with recombinant IFNγ increases the transcription of CD11b and CD18, which correlates with increased surface expression of CR3, and that the effect of IFNγ on the phagocytosis of B. burgdorferi is circumscribed to CR3 activity, because inhibition of CR3 is able to completely diminish the effect of IFNγ on the phagocytosis of the B. burgdorferi . Lastly, our results demonstrate that CR3 is a negative regulator of proinflammatory cytokine induction in macrophages responding to B. burgdorferi . Overall, our data demonstrate roles for CR3 in the binding, phagocytosis and proinflammatory cytokine elicited by B. burgdorferi and shed light on the role of IFNγ in mediating the clearance of the spirochete during Lyme disease.