Uso de lipossomas microestruturados na formulação de vacinas de subunidade protéica HspX para tuberculose
Furkejuvvon:
| Váldodahkki: | |
|---|---|
| Almmustuhttinbeaivi: | 2014 |
| Materiálatiipa: | Master thesis |
| Giella: | por |
| Gáldu: | Repositório Institucional da UFG |
| Download full: | http://repositorio.bc.ufg.br/tede/handle/tede/4700 |
Čoahkkáigeassu: | Tuberculosis is a disease that affects thousands of people in the World. Although Brazil Health Program had achieved the goal of reducing to 50% the rate of death induced by Tuberculosis, this disease continues to be the second cause of death by infectious disease. One of the main problems to control the disease is the low efficacy of BCG vaccine in protecting young adults. The development of new vaccines that induces long lasting immune response or that stimulate the immunity induced by BCG may improve the control of TB spreading. This study evaluated the use of microstructured liposomes containing HspX with or without MPL or CpG DNA adjuvants as vaccine for tuberculosis. The HspX specific humoral and cellular immune responses were compared between the different vaccine formulations. All vaccines containing liposome microparticules and HspX were immunogenic and antigenic. Vaccines formulated with CpG DNA and HspX induced the strongest humoral and cellular immune responses, mainly by generating IFN- and TNF-by both CD4 and CD8 T cells. HspX and MPL mainly induced CD8 T cell activation and humoral specific responses. After protection efficacy evaluation against Mycobacterium tuberculosis challenge, the vaccine formulation that reduced both lung inflammatory lesions and the bacterial load was the microstructured liposome containing HspX and CPG DNA. These results show for the first time the use of microstructured liposome as adjuvant and delivery system in HspX vaccine formulation for tuberculosis. |
Geahča maid: Uso de lipossomas microestruturados na formulação de vacinas de subunidade protéica HspX para tuberculose
- Reação imunoenzimática (ELISA) para detecção de imunoglobulina M, imunoglobulina G e imunoglobulina A contra a proteína rHsp-X (Rv 2031c)de Mycobacterium tuberculosis em pacientes com tuberculose pleural
- Reação imunoenzimática (ELISA) para detecção de imunoglobulina M, imunoglobulina G e imunoglobulina A contra a proteína rHsp-X (Rv 2031c) de mycobacterium tuberculosis em pacientes com tuberculose pleural
- Expressão heterológa e imunolocalização das proteínas HSP30 e catalase peroxissomal identificadas na parede de Paracoccidioides spp. interagindo com macrófagos
- Análise do perfil de expressão de genes da família Hsp70 de Trichoderma asperellum (TR356) durante o micoparasitismo e estresses abióticos
- Avaliação do adjuvante Advax na formulação de vacina de subunidade proteica contra Mycobacterium tuberculosis
- Homeostase de ferro em Paracoccidioides spp.: novos alvos de estudo e estabelecimento de HSP30 como proteína ligante de hemoglobina
