Use of TrypTectCIAAT to determine the effectiveness of treatment of Trypanosoma brucei rhodesiense infections in vervet monkeys (Chlorocebus aethiops) and man.

S. Karanja, J. Ngaira, J. Thuita, Maina-Ngotho, C. Gichuki
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引用次数: 2

Abstract

The vervet monkey (Chlorocebus aethiops) model of sleeping sickness was used to evaluate the effectiveness of TrypTectCIATT in assessing the success of trypanocidal therapy. A retrospective study was therefore conducted on sera collected from monkeys infected with Trypanosoma brucei rhodesiense and treated either curatively with melarsoprol or sub-curatively with diminazene aceturate. In the human survey, 440 sera collected from 96 human patients were tested. These patients were treated with either suramin or melarsoprol depending on the stage of the disease. An extra 56 parasitologically positive pretreatment samples were also tested to aid in determination of the test sensitivity. Results indicated that between 21–28 days post-infection, the test detected trypanosomal antigens in 84.2 % (16/19) of animal samples that were parasitologically positive by the haematocrit centrifugation technique (HCT). In curatively treated animals, 77.8 % (7/9) exhibited positive reaction up to 9 months post-treatment. One animal was positive for trypanosomal antigens for the entire 12 months while one was a non-reactor. From the sub-curatively treated group, 80% (8/10) were detected positive for the entire 12 months while, 2 animals were non-reactors. In the human survey, three patterns of antigen profiles were observed. In some patients, there was fluctuation of antigen levels throughout the 12 months followup period. In others, antigens were detected for the entire 12 months but in decreasing levels. The last group was that of patients with antigens decreasing at different rates to undetectable levels at 12 months post-treatment. The presence of trypanosome positive but antigen negative samples during the study raises a few questions with regards to the sensitivity of the test. It is however evident that the test was able to detect trypanosomal antigens in over 80 % of positive monkey and human serum samples. Consequently, TrypTectCIATT may be an important additional tool in reduction of the follow-up period and determination of success of chemotherapy in sleeping sickness.
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应用TrypTectCIAAT测定黑尾猴和人布氏罗得西亚锥虫感染的治疗效果。
采用黑尾猴(Chlorocebus aethiops)昏睡病模型,评价TrypTectCIATT在评估锥虫治疗成功与否方面的有效性。因此,对感染布氏罗得西亚锥虫的猴子采集的血清进行了回顾性研究,并用美拉胂醇进行治疗或用醋酸氨基苯进行亚治疗。在人类调查中,对从96名人类患者身上收集的440份血清进行了检测。这些患者根据疾病的分期分别用苏拉明或美拉胂醇治疗。另外56个寄生虫学阳性的预处理样品也进行了测试,以帮助确定测试的敏感性。结果表明,在感染后21 ~ 28 d,经红细胞压积离心法(HCT)检测呈寄生虫学阳性的动物标本中检出84.2%(16/19)的锥虫抗原。在治愈治疗的动物中,77.8%(7/9)在治疗后9个月出现阳性反应。一只动物在整个12个月内呈锥虫抗原阳性,而另一只没有反应。在亚治愈治疗组中,80%(8/10)的动物在整个12个月内检测到阳性,2只动物没有反应。在人类调查中,观察到三种类型的抗原谱。在一些患者中,抗原水平在12个月的随访期间出现波动。在其他病例中,抗原在整个12个月内都被检测到,但水平有所下降。最后一组患者的抗原在治疗后12个月以不同的速度下降到无法检测的水平。在研究期间出现的锥虫阳性但抗原阴性的样本提出了一些关于测试敏感性的问题。然而,很明显,该试验能够在80%以上的阳性猴子和人血清样本中检测到锥虫抗原。因此,TrypTectCIATT可能是减少随访时间和确定昏睡病化疗成功的重要附加工具。
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