抗克氏锥虫治疗性疫苗接种后恒河猴心脏功能的安全性和保护作用。
Safety and preservation of cardiac function following therapeutic vaccination against Trypanosoma cruzi in rhesus macaques.
机构信息
Department of Tropical Medicine, School of Public Health and Tropical Medicine, Vector-Borne and Infectious Disease Research Center, Tulane University, New Orleans, LA, USA.
Department of Tropical Medicine, School of Public Health and Tropical Medicine, Vector-Borne and Infectious Disease Research Center, Tulane University, New Orleans, LA, USA.
出版信息
J Microbiol Immunol Infect. 2023 Apr;56(2):400-407. doi: 10.1016/j.jmii.2022.09.003. Epub 2022 Sep 29.
BACKGROUND
Chronic Chagasic cardiomyopathy is responsible for a large disease burden in the Americas, and a therapeutic vaccine would be highly desirable. We tested the safety and efficacy of a therapeutic DNA vaccine encoding antigens TSA-1 and Tc24 for preventing cardiac alterations in experimentally infected macaques. A secondary objective was to evaluate the feasibility of detecting changes in cardiac alterations in these animals.
METHODS
Naïve rhesus macaques were infected with Trypanosoma cruzi and treated with three doses of DNA vaccines.
RESULTS
Blood cell counts and chemistry indicated that therapeutic vaccination was safe, as hepatic and renal function appeared unaffected by the vaccination and/or infection with T. cruzi. Electrocardiographic (ECG) recordings indicated that no marked arrhythmias developed up to 7 months post-infection. Univariate analysis of ECG parameters found no significant differences in any of these parameters between vaccinated and control macaques. However, linear discriminant analysis revealed that control macaques presented clear alterations in their ECG patterns at 7 months post-infection, indicative of the onset of conduction defects and cardiac alterations, and these changes were prevented in vaccine treated macaques.
CONCLUSIONS
This is the first evidence that therapeutic vaccination against T. cruzi can prevent cardiac alterations in non-human primates, strengthening the rationale for developing a human vaccine against Chagas disease.
背景
慢性恰加斯心脏病在美洲造成了很大的疾病负担,如果有一种治疗性疫苗,那将是非常理想的。我们测试了一种编码 TSA-1 和 Tc24 抗原的治疗性 DNA 疫苗预防实验感染猕猴心脏改变的安全性和有效性。次要目标是评估在这些动物中检测心脏改变的可行性。
方法
用克氏锥虫感染幼稚恒河猴,并给予三剂 DNA 疫苗治疗。
结果
血细胞计数和化学分析表明,治疗性疫苗接种是安全的,因为肝功能和肾功能似乎不受疫苗接种和/或克氏锥虫感染的影响。心电图(ECG)记录表明,感染后 7 个月内没有出现明显的心律失常。ECG 参数的单变量分析发现,接种疫苗和对照组猕猴在这些参数中没有显著差异。然而,线性判别分析显示,对照组猕猴在感染后 7 个月时心电图模式发生了明显改变,表明存在传导缺陷和心脏改变,而这些改变在疫苗治疗的猕猴中得到了预防。
结论
这是第一个证明针对克氏锥虫的治疗性疫苗可以预防非人类灵长类动物心脏改变的证据,为开发针对恰加斯病的人类疫苗提供了更强有力的依据。