Paracoccidioidomycosis vaccine

被引:21
|
作者
Travassos, Luiz R. [1 ]
Taborda, Carlos P. [2 ,3 ]
机构
[1] Univ Fed Sao Paulo, Div Cell Biol, Dept Microbiol Immunol & Parasitol, Sao Paulo, Brazil
[2] Univ Sao Paulo, Inst Biomed Sci, Dept Microbiol, Sao Paulo, Brazil
[3] Univ Sao Paulo, Lab Med Mycol IMT SP LIM53, Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
Paracoccidiodes brasiliensis; Gp43; Peptide P10; vaccine; adjuvant; DNA therapy; Th-1 immune response; T-CELL EPITOPE; MURINE PARACOCCIDIOIDOMYCOSIS; 43-KILODALTON GLYCOPROTEIN; PEPTIDE P10; BRASILIENSIS; GP43; ANTIGEN; MICE; IMMUNIZATION; CHEMOTHERAPY;
D O I
10.4161/hv.21283
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Paracoccidioidomycosis is a granulomatous pulmonary infection that is generally controlled by chemotherapy. The efficacy of treatment, however, is limited by the status of the host immune response. The inhibition of a Th-2 immunity or the stimulation of Th-1 cytokines generally increases the efficacy of antifungal drugs.(1) This has been achieved by immunization with an internal peptide of the major diagnostic antigen gp43 of Paracoccidioides brasiliensis. Peptide 10 (QTLIAIHTLAIRYAN) elicits an IFN-gamma rich Th-1 immune response that protects against experimental intratracheal infection by this fungus. The combination of chemotherapy with P10 immunization showed additive protective effect even after 30 d of infection or in anergic mice, rendering in general, increased production of IL-12 and IFN-gamma and reduction of IL-4 and IL-10. Immunotherapy with P10 even in the absence of simultaneous chemotherapy has been effective using various protocols, adjuvants, nanoparticles, P10-primed dendritic cells, and especially a combination of plasmids encoding the P10 minigene and IL-12. Gene therapy, in a long-term infection protocol succeeded in the virtual elimination of the fungus, preserving the lung structure, free from immunopathological side effects.
引用
收藏
页码:1450 / 1453
页数:4
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