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在感染马来布鲁线虫的印度叶猴(食蟹猴)中,成年前期寄生虫和多次定时暴露于感染性幼虫与肢体水肿的发展有关。

Preadult stage parasites and multiple timed exposure to infective larvae are involved in development of limb edema in Brugia malayi-infected Indian leaf monkeys (Presbytis entellus).

作者信息

Murthy P K, Khan M A, Rajani H B, Srivastava V M L

机构信息

Divisions of Parasitology, Central Drug Research Institute, Lucknow 226001, India.

出版信息

Clin Diagn Lab Immunol. 2002 Jul;9(4):913-8. doi: 10.1128/cdli.9.4.913-918.2002.

Abstract

The pathogenesis of filarial limb edema is not known. The role of parasitological variables and parasite-mediated phenomena in the development of limb edema was investigated in the Presbytis entellus-Brugia malayi model. Infection was initiated with subcutaneous inoculation of infective third-stage larvae (L(3)), and the animals were reexposed to different doses of L(3) at the prepatent, patent, and diminishing microfilaremia (0 to 5% of peak microfilaremia count) stages of infection. A large L(3) inoculum size and repeated inoculation in the ankle region during the prepatent, patent, and diminishing microfilaremia stages of infection were found to be necessary for reproducible induction of limb edema. The preadult stage of the parasite was found to be the most potent inducer of limb edema, followed by L(5) and L(4). The presence of the proinflammatory cytokines tumor necrosis factor alpha, interleukin-1beta, and interleukin-6 in edema fluid in the leg receiving the parasite challenge indicated that the limb edema development was due to parasite-mediated cytokine responses. The absence of bacterial infection or anti-streptolysin O titer in the edema fluid and blood indicated that bacterial infection is not necessary for the development of limb edema.

摘要

丝虫性肢体水肿的发病机制尚不清楚。在豚尾叶猴-马来布鲁线虫模型中,研究了寄生虫学变量和寄生虫介导的现象在肢体水肿发展中的作用。通过皮下接种感染性三期幼虫(L(3))引发感染,并在感染的潜伏期、成虫期和微丝蚴血症逐渐减少期(微丝蚴血症峰值计数的0至5%)让动物再次接触不同剂量的L(3)。发现在感染的潜伏期、成虫期和微丝蚴血症逐渐减少期,在踝关节区域接种大量L(3)并重复接种对于可重复诱导肢体水肿是必要的。发现寄生虫的未成热阶段是肢体水肿最有效的诱导因素,其次是L(5)和L(4)。在接受寄生虫攻击的腿部水肿液中存在促炎细胞因子肿瘤坏死因子α、白细胞介素-1β和白细胞介素-6,这表明肢体水肿的发展是由于寄生虫介导的细胞因子反应。水肿液和血液中不存在细菌感染或抗链球菌溶血素O滴度,这表明细菌感染对于肢体水肿的发展不是必需的。

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