Probst R J, Wellde B T, Lawyer P G, Stiteler J S, Rowton E D
Division of Veterinary Medicine, Walter Reed Army Institute of Research, Silver Spring, Maryland 20910-7500, USA.
Med Vet Entomol. 2001 Mar;15(1):12-21. doi: 10.1046/j.1365-2915.2001.00283.x.
Leishmaniasis research needs a near-human model for investigations of natural infection processes, immunological responses and evaluation of treatments. Therefore, we developed a reproducible system using Leishmania major Yakimoff & Schokhor (Trypanosomatidae: Kinetoplastida), the cause of Old World zoonotic cutaneous leishmaniasis (ZCL), transmitted to rhesus monkeys Macaca mulatta (Zimmerman) (Primates: Cercopithecidae) by sandfly bites of experimentally infected Phlebotomus papatasi (Scopoli) (Diptera: Psychodidae). Eight monkeys of presumed Indian origin (Leishmania naive) were exposed to bites of female sandflies that had been infected with L. major by membrane-feeding on human blood seeded with amastigotes isolated from hamster footpad lesions. Infection rates of membrane-fed sandflies averaged > 85% seven days after the infective feed, with uniformly high numbers of promastigotes in the stomodaeal valve region of the sandfly gut. Nodules and ulcerating dermal lesions developed on 7/8 monkeys 2-4 weeks post-bite and persisted for 3-7 months. Monkeys also developed satellite lesions beyond the area of sandfly bites on the head, but not on the chest. Three re-challenged monkeys developed lesions that healed faster than lesions from their primary challenges. After infection, monkeys developed delayed type hypersensitivity (DTH) responses to a panel of Leishmania skin test antigens (LSTA) and, when tested by ELISA and IFA, showed significant post-infection antibody titres which typically rose for approximately 170 days and then gradually receded during the next 100 days following the first challenge. After the second challenge, antibody titres spiked higher within approximately 50 days and receded more rapidly. In contrast, four rhesus macaques of Chinese origin developed no lesions following infected sandfly bites, although they raised antibodies and LSTA reactions, indicating subclinical infection.
利什曼病研究需要一种近乎人类的模型来研究自然感染过程、免疫反应以及评估治疗方法。因此,我们利用硕大利什曼原虫(Yakimoff & Schokhor,锥虫科:动质体目)开发了一种可重复的系统,该原虫是旧世界人畜共患皮肤利什曼病(ZCL)的病原体,通过对实验感染的巴氏白蛉(Scopoli,双翅目:毛蠓科)叮咬恒河猴(Zimmerman,灵长目:猕猴科)来传播。八只推测为印度来源(未感染利什曼原虫)的猴子被暴露于经膜饲接种从仓鼠足垫病变分离的无鞭毛体后感染了硕大利什曼原虫的雌性白蛉叮咬。在感染性饲血七天后,经膜饲的白蛉感染率平均>85%,白蛉肠道口道瓣膜区域的前鞭毛体数量一致很高。叮咬后2 - 4周,8只猴子中有7只出现结节和溃疡性皮肤病变,并持续3 - 7个月。猴子头部白蛉叮咬区域之外也出现了卫星状病变,但胸部没有。三只再次受到攻击的猴子所出现的病变愈合速度比初次攻击时的病变更快。感染后,猴子对一组利什曼原虫皮肤试验抗原(LSTA)产生了迟发型超敏反应(DTH),并且通过ELISA和IFA检测时,显示出感染后显著的抗体滴度——通常在首次攻击后约170天上升,然后在接下来的100天内逐渐下降。第二次攻击后,抗体滴度在约50天内飙升得更高,且下降得更快。相比之下,四只中国来源的恒河猴在被感染白蛉叮咬后未出现病变,尽管它们产生了抗体和LSTA反应,表明存在亚临床感染。