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米替福新、米替福新联合别嘌醇与别嘌醇在治疗内脏利什曼病犬中的对比研究。

Comparative study of the use of miltefosine, miltefosine plus allopurinol, and allopurinol in dogs with visceral leishmaniasis.

机构信息

Program of Postgraduate in Veterinary Sciences, Faculty of Veterinary Medicine, Federal University of Mato Grosso (UFMT), Av. Fernando Corrêa da Costa, 2367, Bairro Boa Esperança, CEP 78060-900, Cuiabá, MT, Brazil.

Program of Postgraduate in Veterinary Sciences, Faculty of Veterinary Medicine, Federal University of Mato Grosso (UFMT), Av. Fernando Corrêa da Costa, 2367, Bairro Boa Esperança, CEP 78060-900, Cuiabá, MT, Brazil.

出版信息

Exp Parasitol. 2020 Oct;217:107947. doi: 10.1016/j.exppara.2020.107947. Epub 2020 Jul 3.

Abstract

Visceral leishmaniasis (VL) is an infectious disease caused by the protozoan parasite Leishmania (Leishmania) infantum, an intracytoplasmic parasite that affects humans and other species of domestic and wild mammals. In Brazil, the treatment of canine visceral leishmaniasis (CVL) with miltefosine has been implemented since 2016, and the reports on the clinical and immunological conditions of treated dogs are scarce. Thus, this study aimed to assess and monitor the clinical, laboratory, and immunological condition of dogs with CVL before (D) and after (D) using three pharmacotherapeutic protocols: miltefosine monotherapy (Milteforan™, Virbac) (G1), miltefosine plus allopurinol (G2), and allopurinol monotherapy (G3). Forty-five dogs with CVL were assigned to one of three treatment groups. The dogs were evaluated for clinical signs, was well as haematological, biochemical, serological, and cytokine levels. Significant reduction in clinical scores was observed in all protocols, with no differences between groups. We did not observe a clinical cure in any of the dogs in the groups. Haematological and biochemical parameters showed slow recovery, with better results observed in G2. Anti-Leishmania antibody titre remained increased in all groups. The quantification of serum cytokines demonstrated a mixed Th1/Th2 profile in CVL. The IL-2 levels decreased in all groups after treatment. Evaluation of IFN-y and IL-10 did not show changes in the groups analysed, and it did not contribute to short term therapeutic monitoring. All therapeutic protocols promoted, to varying degrees, an improvement in the general condition (clinical signs, haematological, and biochemical levels) of the animals. Through clinical-pathological exams, we found that the combination of miltefosine plus allopurinol promoted better effects in the short-term, representing the best choice for the treatment of CVL, even when compared to the only therapeutic protocol allowed in Brazil, miltefosine monotherapy. Through the quantification of cytokines, IL-2 proved to be a potential therapeutic marker for the monitoring and follow-up of dogs with CVL.

摘要

内脏利什曼病(VL)是一种由原生动物寄生虫利什曼原虫(Leishmania)引起的传染病,是一种细胞内寄生虫,影响人类和其他家养和野生哺乳动物物种。在巴西,自 2016 年以来,已用米替福新治疗犬内脏利什曼病(CVL),关于接受治疗的犬的临床和免疫状况的报告很少。因此,本研究旨在评估和监测 CVL 犬在使用三种药物治疗方案之前(D)和之后(D)的临床、实验室和免疫状况:米替福新单药治疗(MilteforanTM,Virbac)(G1)、米替福新加别嘌醇(G2)和别嘌醇单药治疗(G3)。将 45 只患有 CVL 的犬分配到三个治疗组中的一个。评估犬的临床症状以及血液学、生化学、血清学和细胞因子水平。所有方案均观察到临床评分显著降低,组间无差异。我们没有观察到任何一组中的犬临床治愈。血液学和生化学参数恢复缓慢,G2 组结果更好。抗利什曼原虫抗体滴度在所有组中均保持升高。血清细胞因子的定量显示 CVL 呈混合 Th1/Th2 表型。所有组在治疗后 IL-2 水平均降低。对 IFN-y 和 IL-10 的评估显示分析组无变化,并且不能用于短期治疗监测。所有治疗方案都在不同程度上改善了动物的一般状况(临床症状、血液学和生化学水平)。通过临床病理检查,我们发现米替福新加别嘌醇联合治疗在短期内产生了更好的效果,与巴西允许的唯一治疗方案米替福新单药治疗相比,代表了治疗 CVL 的最佳选择。通过细胞因子的定量,IL-2 被证明是监测和随访 CVL 犬的潜在治疗标志物。

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