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Vaccine and immunotherapeutic approaches for the prevention of cryptococcosis: lessons learned from animal models.预防隐球菌病的疫苗和免疫治疗方法:从动物模型中汲取的经验教训。
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2
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CD4 T Cells Orchestrate Lethal Immune Pathology despite Fungal Clearance during Meningoencephalitis.CD4 T 细胞在脑膜脑炎中尽管清除了真菌,但仍能协调致命的免疫病理。
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Three Models of Vaccination Strategies Against Cryptococcosis in Immunocompromised Hosts Using Heat-Killed Δ.三种针对免疫功能低下宿主隐球菌病的疫苗接种策略模型,使用热灭活的 Δ.
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Cryptococcus neoformans Chitin Synthase 3 Plays a Critical Role in Dampening Host Inflammatory Responses.新型隐球菌几丁质合成酶 3 在抑制宿主炎症反应中发挥关键作用。
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The primary target organ of Cryptococcus gattii is different from that of Cryptococcus neoformans in a murine model.在小鼠模型中,新型隐球菌的主要靶器官与格特隐球菌不同。
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Protective interaction of human phagocytic APC subsets with induces genes associated with metabolism and antigen presentation.与 相互作用可保护人吞噬性 APC 亚群,诱导与代谢和抗原呈递相关的基因。
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Infection Induces IL-17 Production by Promoting STAT3 Phosphorylation in CD4 T Cells.感染通过促进 CD4 T 细胞中 STAT3 的磷酸化诱导 IL-17 的产生。
Front Immunol. 2022 May 27;13:872286. doi: 10.3389/fimmu.2022.872286. eCollection 2022.
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A Call to Arms: Quest for a Cryptococcal Vaccine.《行动呼吁:寻找隐球菌疫苗》
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Antifungal Therapy: New Advances in the Understanding and Treatment of Mycosis.抗真菌治疗:真菌病认识与治疗的新进展
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Cryptococcus and Phagocytes: Complex Interactions that Influence Disease Outcome.隐球菌与吞噬细胞:影响疾病转归的复杂相互作用
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10
Is Development of a Vaccine against Cryptococcus neoformans Feasible?开发针对新型隐球菌的疫苗可行吗?
PLoS Pathog. 2015 Jun 18;11(6):e1004843. doi: 10.1371/journal.ppat.1004843. eCollection 2015 Jun.

本文引用的文献

1
Cryptococcus neoformans galactoxylomannan is a potent negative immunomodulator, inspiring new approaches in anti-inflammatory immunotherapy.新型隐球菌半乳甘露聚糖是一种有效的负性免疫调节剂,为抗炎免疫治疗提供了新方法。
Immunotherapy. 2011 Aug;3(8):997-1005. doi: 10.2217/imt.11.86.
2
Fungicidal monoclonal antibody C7 interferes with iron acquisition in Candida albicans.杀菌单克隆抗体 C7 干扰白念珠菌中铁的获取。
Antimicrob Agents Chemother. 2011 Jul;55(7):3156-63. doi: 10.1128/AAC.00892-10. Epub 2011 Apr 25.
3
Protective immunity against experimental pulmonary cryptococcosis in T cell-depleted mice.T细胞耗竭小鼠对实验性肺隐球菌病的保护性免疫。
Clin Vaccine Immunol. 2011 May;18(5):717-23. doi: 10.1128/CVI.00036-11. Epub 2011 Mar 30.
4
Effect of cytokine interplay on macrophage polarization during chronic pulmonary infection with Cryptococcus neoformans.细胞因子相互作用对新型隐球菌慢性肺部感染期间巨噬细胞极化的影响。
Infect Immun. 2011 May;79(5):1915-26. doi: 10.1128/IAI.01270-10. Epub 2011 Mar 7.
5
Role of IL-17A on resolution of pulmonary C. neoformans infection.IL-17A 在肺部新型隐球菌感染消退中的作用。
PLoS One. 2011 Feb 17;6(2):e17204. doi: 10.1371/journal.pone.0017204.
6
Expanding fungal pathogenesis: Cryptococcus breaks out of the opportunistic box.拓展真菌发病机制:新型隐球菌打破机会主义框框。
Nat Rev Microbiol. 2011 Mar;9(3):193-203. doi: 10.1038/nrmicro2522.
7
Evaluation of Cryptococcus neoformans galactoxylomannan-protein conjugate as vaccine candidate against murine cryptococcosis.评估新型隐球菌半乳甘露聚糖-蛋白结合物作为抗鼠隐球菌病疫苗候选物。
Vaccine. 2011 Feb 24;29(10):1891-8. doi: 10.1016/j.vaccine.2010.12.134. Epub 2011 Jan 14.
8
Interleukin-17 is not required for classical macrophage activation in a pulmonary mouse model of Cryptococcus neoformans infection.白细胞介素-17 对于新型隐球菌感染肺部小鼠模型中经典的巨噬细胞激活并非必需。
Infect Immun. 2010 Dec;78(12):5341-51. doi: 10.1128/IAI.00845-10. Epub 2010 Oct 4.
9
Emergence of Cryptococcus gattii-- Pacific Northwest, 2004-2010.新型隐球菌——太平洋西北地区,2004-2010 年。
MMWR Morb Mortal Wkly Rep. 2010 Jul 23;59(28):865-8.
10
Radioimmunotherapy is more effective than antifungal treatment in experimental cryptococcal infection.放射性免疫疗法比抗真菌治疗更有效治疗实验性隐球菌感染。
J Infect Dis. 2010 Aug 15;202(4):633-7. doi: 10.1086/654813.

预防隐球菌病的疫苗和免疫治疗方法:从动物模型中汲取的经验教训。

Vaccine and immunotherapeutic approaches for the prevention of cryptococcosis: lessons learned from animal models.

作者信息

Hole Camaron R, Wormley Floyd L

机构信息

Department of Biology, The University of Texas at San Antonio San Antonio, TX, USA.

出版信息

Front Microbiol. 2012 Aug 28;3:291. doi: 10.3389/fmicb.2012.00291. eCollection 2012.

DOI:10.3389/fmicb.2012.00291
PMID:22973262
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3428735/
Abstract

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.

摘要

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。