Efeito da terapia antituberculose na expressão dos receptores TLR-2 e 4, do fator de transcrição Foxp3, da Óxido Nítrico Sintase Induzível, no perfil de citocinas e nas alterações genóticas
Carregando...
Data
2012-02-15
Autores
Oliveira, Larissa Ragozo Cardoso de [UNESP]
Título da Revista
ISSN da Revista
Título de Volume
Editor
Universidade Estadual Paulista (Unesp)
Resumo
A tuberculose permanece como um dos principais problemas de saúde pública no Brasil e no mundo. Tem como principal agente o Mycobacterium tuberculosis, e é uma doença letal sem tratamento, e seu controle é dificultado pela longa duração e ausência de marcadores, para medir o sucesso ou a falha deste. Os TLRs são receptores que após o reconhecimento de produtos microbianos, ativam a resposta inata e adaptativa. Assim, os receptores TLRs e as citocinas possuem um papel chave na defesa contra o bacilo. Considerando a ausência de informações na literatura em relação à resposta imune de pacientes com tuberculose pulmonar durante o tratamento antituberculose, principalmente em relação à interação inicial do M. tuberculosis com as células da imunidade inata e de seu papel, na indução da resposta adaptativa, através dos receptores TLR, estudos neste sentido, são necessários para se compreender melhor como é a resposta imune do hospedeiro contra o bacilo, frente ao tratamento. Assim, o objetivo deste trabalho foi avaliar a expressão dos receptores TLR2 e TLR4, do fator de transcrição Foxp3 e da enzima óxido nítrico sintase induzível (iNOS), produção e expressão de citocinas, e alterações genotóxicas em pacientes durante o tratamento antituberculose. Foram coletadas amostras de sangue total dos controles saudáveis PPD+ em um único momento (G1) e de pacientes (G1) em três momentos diferentes: M1: início; M2: terceiro mês e M3: ao sexto mês de tratamento antituberculose. Após a obtenção das células mononucleares do sangue periférico (PBMC), as concentrações celulares foram ajustadas para a realização da qPCR, da citometria de fluxo e do teste do cometa. Pacientes com tuberculose pulmonar apresentaram expressão gênica, e na superfície célular de linfócitos e...
Tuberculosis (TB) remains a major public health problems in Brazil and worldwide. Its main agent Mycobacterium tuberculosis, and is a lethal disease without treatment, and its control is hampered by the long duration and lack of markers to measure the success or failure of this. The TLRs are receptors that after the recognition of microbial products, activate innate and adaptive response. Thus, TLRs receptors and cytokine have a key role in defense against the bacillus. Considering the absence of information in the literature regarding the immune response of patients with pulmonary tuberculosis during antituberculosis treatment, especially in relation to the initial interaction of M. tuberculosis with the cells of innate immunity and its role in the induction of adaptive response through the TLR receptors, studies in this direction are needed to better understand how the host immune response against the bacillus, towards treatment. The objective of this study was to evaluate the expression of TLR2 and TLR4 receptors, the transcription factor Foxp3 and inducible nitric oxide synthase (iNOS) production and expression of cytokines and genotoxic alterations in patients during TB treatment. Samples were collected from whole blood of healthy PPD + controls in a single moment (G1) and patients (G1) at three different moments: M1: start, M2, M3, and the third month, the sixth month of TB treatment. After obtaining the peripheral blood mononuclear cells (PBMC) and cell concentrations were adjusted to carry out the qPCR, flow cytometry and testing of the comet. Patients with pulmonary tuberculosis showed gene expression and cell surface of lymphocytes and monocytes from TLR2 and TLR4 greater than the control subjects, both in M1, M2 and M3. However, the expression and cell surface receptor TLR2 was... (Complete abstract click electronic access below)
Tuberculosis (TB) remains a major public health problems in Brazil and worldwide. Its main agent Mycobacterium tuberculosis, and is a lethal disease without treatment, and its control is hampered by the long duration and lack of markers to measure the success or failure of this. The TLRs are receptors that after the recognition of microbial products, activate innate and adaptive response. Thus, TLRs receptors and cytokine have a key role in defense against the bacillus. Considering the absence of information in the literature regarding the immune response of patients with pulmonary tuberculosis during antituberculosis treatment, especially in relation to the initial interaction of M. tuberculosis with the cells of innate immunity and its role in the induction of adaptive response through the TLR receptors, studies in this direction are needed to better understand how the host immune response against the bacillus, towards treatment. The objective of this study was to evaluate the expression of TLR2 and TLR4 receptors, the transcription factor Foxp3 and inducible nitric oxide synthase (iNOS) production and expression of cytokines and genotoxic alterations in patients during TB treatment. Samples were collected from whole blood of healthy PPD + controls in a single moment (G1) and patients (G1) at three different moments: M1: start, M2, M3, and the third month, the sixth month of TB treatment. After obtaining the peripheral blood mononuclear cells (PBMC) and cell concentrations were adjusted to carry out the qPCR, flow cytometry and testing of the comet. Patients with pulmonary tuberculosis showed gene expression and cell surface of lymphocytes and monocytes from TLR2 and TLR4 greater than the control subjects, both in M1, M2 and M3. However, the expression and cell surface receptor TLR2 was... (Complete abstract click electronic access below)
Descrição
Palavras-chave
Tuberculose - Tratamento, Aparelho repiratório - Doenças - Tratamento, Cytokines, Antioxidants, DNA damage
Como citar
OLIVEIRA, Larissa Ragozo Cardoso de. Efeito da terapia antituberculose na expressão dos receptores TLR-2 e 4, do fator de transcrição Foxp3, da Óxido Nítrico Sintase Induzível, no perfil de citocinas e nas alterações genóticas. 2012. 127 f. Dissertação (mestrado) - Universidade Estadual Paulista, Faculdade de Medicina de Botucatu, 2012.