Manna Laura, Reale Stefano, Vitale Fabrizio, Picillo Esther, Pavone Luigi Michele, Gravino Angelo Elio
Dipartimento di Scienze Cliniche Veterinarie, Università di Napoli Federico II, Napoli, Italy.
Vet J. 2008 Aug;177(2):279-82. doi: 10.1016/j.tvjl.2007.04.013. Epub 2007 Jun 5.
A real-time PCR assay was exploited for monitoring the Leishmania DNA load in different tissues from 18 naturally-infected dogs before and after treatment with a combination of meglumine antimoniate (100mg/kg/day, subcutaneously) and allopurinol (10mg/kg/day, orally) for 30 days. After the combined therapy, allopurinol was continued at the same dose until the end of the observation period. Whole blood samples, lymph node aspirates, and skin biopsies were collected at the time of diagnosis, 1 month after starting therapy, and every 3 months for 2 years. In six dogs parasite load assessments continued every 6 months for a further 3 years. At each assessment, the dogs were examined for signs of disease and a clinical score was recorded. At diagnosis, the highest Leishmania DNA load was detected in lymph node aspirates. From 1-6 months post-therapy a general improvement in clinical conditions was recorded in all dogs, which correlated with a decrease in the parasite DNA load in all tested tissues, even though it was less pronounced in lymph node aspirates. In the period from 9-24 months post-therapy, a re-increase in parasite load was observed in the tissues of some dogs, concomitant with a disease relapse. The results show that the combined therapy with meglumine antimoniate and allopurinol promoted a clinical improvement which was accompanied by a reduction in the parasitic load in the blood, skin and lymph nodes but, even after long period of allopurinol administration alone, Leishmania may persist in dog tissues.
利用实时聚合酶链反应(PCR)检测法监测18只自然感染利什曼原虫的犬在接受葡甲胺锑酸盐(100mg/kg/天,皮下注射)和别嘌呤醇(10mg/kg/天,口服)联合治疗30天前后不同组织中的利什曼原虫DNA载量。联合治疗后,别嘌呤醇以相同剂量持续给药直至观察期结束。在诊断时、开始治疗后1个月以及之后2年每3个月采集全血样本、淋巴结穿刺液和皮肤活检样本。在6只犬中,寄生虫载量评估在接下来的3年中每6个月继续进行一次。每次评估时,检查犬的疾病体征并记录临床评分。诊断时,在淋巴结穿刺液中检测到最高的利什曼原虫DNA载量。治疗后1至6个月,所有犬的临床状况普遍改善,这与所有检测组织中寄生虫DNA载量的降低相关,尽管在淋巴结穿刺液中这种降低不太明显。在治疗后9至24个月期间,一些犬的组织中观察到寄生虫载量再次增加,同时伴有疾病复发。结果表明,葡甲胺锑酸盐和别嘌呤醇联合治疗促进了临床改善,同时血液、皮肤和淋巴结中的寄生虫载量降低,但即使在长期单独使用别嘌呤醇后,利什曼原虫仍可能在犬组织中持续存在。