Cell Biology Division, Department of Microbiology, Federal University of São Paulo, São Paulo, Brazil.
Hum Vaccin Immunother. 2012 Oct;8(10):1450-3. doi: 10.4161/hv.21283. Epub 2012 Aug 16.
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-γ 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-γ 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.
球孢子菌病是一种肺部肉芽肿性感染,通常可以通过化疗控制。然而,治疗效果受到宿主免疫反应状态的限制。抑制 Th-2 免疫或刺激 Th-1 细胞因子通常会增加抗真菌药物的疗效。(1)这可以通过用巴西副球孢子菌主要诊断抗原 gp43 的内部肽免疫来实现。肽 10(QTLIAIHTLAIRYAN)引发富含 IFN-γ的 Th-1 免疫反应,可预防该真菌的实验性气管内感染。即使在感染 30 天后或在无反应性小鼠中,化疗与 P10 免疫结合也显示出相加的保护作用,导致 IL-12 和 IFN-γ的产生增加,IL-4 和 IL-10 的减少。使用各种方案、佐剂、纳米颗粒、P10 引发的树突状细胞,特别是编码 P10 小基因和 IL-12 的质粒的组合,即使在没有同时化疗的情况下,P10 免疫治疗也具有疗效。在长期感染方案中,基因治疗成功地几乎消除了真菌,同时保持了肺部结构,没有免疫病理副作用。