Laboratório de Parasitologia, Instituto de Ciências Biomédicas, Universidade Federal de Uberlandia. Av. Pará, no. 1720 Bloco 4C, Campus Umuarama, Uberlandia, Minas Gerais, Brazil.
Exp Parasitol. 2010 Jul;125(3):297-303. doi: 10.1016/j.exppara.2010.02.007. Epub 2010 Feb 14.
This study aimed to determine the pre-patent period and to evaluate the kinetics of cyst elimination and the systemic humoral (IgA, IgG(1), IgG(2a), IgM, IgE) and intestinal secretory (IgA) immune responses in gerbils (Meriones unguiculatus) experimentally innoculated with different doses of Giardia duodenalis trophozoites. Forty-eight animals aged 6-8 weeks were used, equally distributed among six groups, five groups innoculated with different doses of trophozoites (10(1), 10(2), 10(3), 10(4), 10(5)) and one control (non-infected) group. Coproparasitological examinations were carried out daily up to 91 days after inoculation (d.a.i.) to determine the pre-patent period and the kinetics of cyst elimination. Blood and stool samples were weekly collected for antibody assays. The pre-patent period was observed from the 9 d.a.i. onwards, with intermittent elimination of variable quantities of cysts up to 27 d.a.i.. All infected gerbils, irrespective of the dose received, were able to mount systemic humoral immune responses as evidenced by specific IgM titers from 7 to 28 d.a.i., corresponding to the peak of cyst elimination, followed by high and persistent IgG1 titers. Intestinal secretory responses were also seen with two peaks of fecal IgA titers, corresponding to IgM and IgG1 response peaks, respectively. In conclusion, systemic and intestinal humoral immune responses were related to the control of giardiasis in this experimental model.
本研究旨在确定贾第虫(Giardia duodenalis)滋养体感染的潜伏期,并评估感染期间囊包排出动力学、血清(IgA、IgG1、IgG2a、IgM、IgE)和肠分泌型(IgA)免疫应答的动力学。实验采用 6-8 周龄沙鼠 48 只,随机分为 6 组,每组 8 只,分别感染不同剂量的滋养体(101、102、103、104、105)或不感染(对照组)。从接种后 91 天(d.a.i.)内每天采集粪便样本进行粪检以确定潜伏期和囊包排出动力学,每周采集血液样本进行抗体检测。感染后第 9 天开始出现潜伏期,感染初期间断排出少量囊包,可持续至第 27 天。所有感染沙鼠均能产生系统的体液免疫应答,感染后第 7-28 天 IgM 滴度升高,达到峰值,随后 IgG1 持续高滴度;同时也观察到了肠分泌型免疫应答,粪便 IgA 出现 2 个高峰,分别与 IgM 和 IgG1 抗体应答的高峰相对应。综上所述,本实验模型中系统和肠道体液免疫应答与贾第虫病的控制有关。