Hole Camaron R, Wormley Floyd L
Department of Biology, The University of Texas at San Antonio San Antonio, TX, USA.
Front Microbiol. 2012 Aug 28;3:291. doi: 10.3389/fmicb.2012.00291. eCollection 2012.
Cryptococcus neoformans and C. gattii, the predominant etiological agents of cryptococcosis, can cause life-threatening infections of the central nervous system in immunocompromised and immunocompetent individuals. Cryptococcal meningoencephalitis is the most common disseminated fungal infection in AIDS patients, and C. neoformans remains the third most common invasive fungal infection among organ transplant recipients. Current anti-fungal drug therapies are oftentimes rendered ineffective due to drug toxicity, the emergence of drug resistant organisms, and/or the inability of the host's immune defenses to assist in eradication of the yeast. Therefore, there remains an urgent need for the development of immune-based therapies and/or vaccines to combat cryptococcosis. Studies in animal models have demonstrated the efficacy of various vaccination strategies and immune therapies to induce protection against cryptococcosis. This review will summarize the lessons learned from animal models supporting the feasibility of developing immunotherapeutics and vaccines to prevent cryptococcosis.
新型隐球菌和格特隐球菌是隐球菌病的主要病原体,可在免疫功能低下和免疫功能正常的个体中引起危及生命的中枢神经系统感染。隐球菌性脑膜脑炎是艾滋病患者中最常见的播散性真菌感染,新型隐球菌仍是器官移植受者中第三常见的侵袭性真菌感染。由于药物毒性、耐药菌的出现和/或宿主免疫防御无法协助根除酵母菌,目前的抗真菌药物治疗常常无效。因此,迫切需要开发基于免疫的疗法和/或疫苗来对抗隐球菌病。动物模型研究已经证明了各种疫苗接种策略和免疫疗法在诱导针对隐球菌病的保护方面的有效性。本综述将总结从动物模型中学到的经验教训,这些经验教训支持开发免疫治疗药物和疫苗以预防隐球菌病的可行性。