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1.
PLoS Pathog ; 10(6): e1004190, 2014 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-24968056

RESUMO

Tuberculosis is still a major health problem worldwide. Currently it is not known what kind of immune responses lead to successful control and clearance of Mycobacterium tuberculosis. This gap in knowledge is reflected by the inability to develop sufficient diagnostic and therapeutic tools to fight tuberculosis. We have used the Mycobacterium marinum infection model in the adult zebrafish and taken advantage of heterogeneity of zebrafish population to dissect the characteristics of adaptive immune responses, some of which are associated with well-controlled latency or bacterial clearance while others with progressive infection. Differences in T cell responses between subpopulations were measured at the transcriptional level. It was discovered that a high total T cell level was usually associated with lower bacterial loads alongside with a T helper 2 (Th2)-type gene expression signature. At late time points, spontaneous reactivation with apparent symptoms was characterized by a low Th2/Th1 marker ratio and a substantial induction of foxp3 reflecting the level of regulatory T cells. Characteristic gata3/tbx21 has potential as a biomarker for the status of mycobacterial disease.


Assuntos
Imunidade Adaptativa , Modelos Animais de Doenças , Infecções por Mycobacterium não Tuberculosas/imunologia , Mycobacterium marinum/imunologia , Células Th2/imunologia , Peixe-Zebra/imunologia , Algoritmos , Animais , Animais Geneticamente Modificados , Carga Bacteriana , Biomarcadores/sangue , Biomarcadores/metabolismo , Progressão da Doença , Fatores de Transcrição Forkhead/sangue , Fatores de Transcrição Forkhead/genética , Fatores de Transcrição Forkhead/metabolismo , Fator de Transcrição GATA3/sangue , Fator de Transcrição GATA3/genética , Fator de Transcrição GATA3/metabolismo , Regulação da Expressão Gênica , Contagem de Linfócitos , Linfopoese , Viabilidade Microbiana , Mutação , Infecções por Mycobacterium não Tuberculosas/sangue , Infecções por Mycobacterium não Tuberculosas/metabolismo , Infecções por Mycobacterium não Tuberculosas/microbiologia , Mycobacterium marinum/crescimento & desenvolvimento , Mycobacterium marinum/isolamento & purificação , Proteínas com Domínio T/sangue , Proteínas com Domínio T/genética , Proteínas com Domínio T/metabolismo , Células Th1/imunologia , Células Th1/metabolismo , Células Th1/microbiologia , Células Th1/patologia , Células Th2/metabolismo , Células Th2/microbiologia , Células Th2/patologia , Regulação para Cima , Peixe-Zebra/genética , Peixe-Zebra/metabolismo , Peixe-Zebra/microbiologia , Proteínas de Peixe-Zebra/sangue , Proteínas de Peixe-Zebra/genética , Proteínas de Peixe-Zebra/metabolismo
2.
PLoS One ; 12(7): e0181942, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28742838

RESUMO

Tuberculosis (TB) remains a major global health challenge and the development of a better vaccine takes center stage in fighting the disease. For this purpose, animal models that are capable of replicating the course of the disease and are suitable for the early-stage screening of vaccine candidates are needed. A Mycobacterium marinum infection in adult zebrafish resembles human TB. Here, we present a pre-clinical screen for a DNA-based tuberculosis vaccine in the adult zebrafish using an M. marinum infection model. We tested 15 antigens representing different types of mycobacterial proteins, including the Resuscitation Promoting factors (Rpf), PE/PPE protein family members, other membrane proteins and metabolic enzymes. The antigens were expressed as GFP fusion proteins, facilitating the validation of their expression in vivo. The efficiency of the antigens was tested against a low-dose intraperitoneal M. marinum infection (≈ 40 colony forming units), which mimics a primary M. tuberculosis infection. While none of the antigens was able to completely prevent a mycobacterial infection, four of them, namely RpfE, PE5_1, PE31 and cdh, led to significantly reduced bacterial burdens at four weeks post infection. Immunization with RpfE also improved the survival of the fish against a high-dose intraperitoneal injection with M. marinum (≈ 10.000 colony forming units), resembling the disseminated form of the disease. This study shows that the M. marinum infection model in adult zebrafish is suitable for the pre-clinical screening of tuberculosis vaccines and presents RpfE as a potential antigen candidate for further studies.


Assuntos
Antígenos de Bactérias/imunologia , Doenças dos Peixes/prevenção & controle , Infecções por Mycobacterium não Tuberculosas/prevenção & controle , Mycobacterium marinum/imunologia , Vacinas contra a Tuberculose/uso terapêutico , Animais , Antígenos de Bactérias/uso terapêutico , Modelos Animais de Doenças , Doenças dos Peixes/imunologia , Doenças dos Peixes/microbiologia , Infecções por Mycobacterium não Tuberculosas/imunologia , Infecções por Mycobacterium não Tuberculosas/veterinária , Peixe-Zebra/imunologia , Peixe-Zebra/microbiologia
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