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黑猩猩的实验性盘尾丝虫病。细胞介导的免疫反应,以及感染旋盘尾丝虫时白细胞介素-1和白细胞介素-2的产生及作用。

Experimental onchocerciasis in chimpanzees. Cell-mediated immune responses, and production and effects of IL-1 and IL-2 with Onchocerca volvulus infection.

作者信息

Soboslay P T, Dreweck C M, Taylor H R, Brotman B, Wenk P, Greene B M

机构信息

Department of Medicine, Case Western Reserve University, Cleveland, OH 44106.

出版信息

J Immunol. 1991 Jul 1;147(1):346-53.

PMID:2051025
Abstract

Nine of eighteen chimpanzees inoculated with infective third-stage larvae of Onchocerca volvulus developed patent infection with microfilariae in skin biopsies. In all infected chimpanzees the in vitro cellular reactivity to O. volvulus adult worm-derived Ag (OvAg) increased significantly after exposure to third-stage larvae. However, during prepatency the in vitro cellular responses to OvAg decreased gradually in subsequently mf positive (patent) animals, and returned with patency to values not different to those before infection. In non-patent chimpanzees cellular responses remained significantly higher than before infection. Stimulation of PBMC in vitro with bacterial Ag and mitogen did not show any differences between the experimental groups through 20 months p.i. The addition of exogenous IL-2 did not restore the impaired responses of PBMC to OvAg in patent animals. Exogenous IL-2 elicited an additive increase of the cellular response to OvAg in nonpatent, and a mitogenic effect to OvAg in patent animals. Selective depletion of adherent, suppressor/cytotoxic (CD8+), NK cells (CD16+) and the use of autologous serum had no effect on antigenic and mitogenic cellular responsiveness. OvAg-induced IL-2 production decreased after patency, whereas, IL-1 production was significantly greater in both patent and nonpatent than in control chimpanzees. In summary, these data demonstrate that experimental O. volvulus infection in chimpanzees stimulated a substantial cell-mediated immune response. In patent chimpanzees an OvAg-specific cellular hyporesponsiveness occurred before onset of patency, possibly due to decreased IL-2 production and responsiveness.

摘要

18只接种旋盘尾丝虫感染性三期幼虫的黑猩猩中,有9只在皮肤活检中出现了微丝蚴的显性感染。在所有受感染的黑猩猩中,暴露于三期幼虫后,对旋盘尾丝虫成虫来源抗原(OvAg)的体外细胞反应性显著增加。然而,在潜伏期,随后出现微丝蚴阳性(显性)的动物对OvAg的体外细胞反应逐渐降低,并在出现显性感染时恢复到与感染前无差异的值。在未出现显性感染的黑猩猩中,细胞反应仍显著高于感染前。在感染后20个月内,用细菌抗原和丝裂原体外刺激外周血单核细胞(PBMC),各实验组之间未显示出任何差异。添加外源性白细胞介素-2(IL-2)并不能恢复显性感染动物PBMC对OvAg受损的反应。外源性IL-2在未出现显性感染的动物中引起对OvAg细胞反应的累加性增加,在显性感染动物中对OvAg产生促有丝分裂作用。选择性去除贴壁细胞、抑制性/细胞毒性(CD8+)细胞、自然杀伤细胞(CD16+)以及使用自体血清对抗抗原性和促有丝分裂细胞反应性均无影响。显性感染后,OvAg诱导的IL-2产生减少,而在显性感染和未出现显性感染的黑猩猩中,IL-1的产生均显著高于对照黑猩猩。总之,这些数据表明,黑猩猩中的实验性旋盘尾丝虫感染刺激了大量的细胞介导免疫反应。在显性感染的黑猩猩中,在显性感染开始前出现了OvAg特异性细胞低反应性,这可能是由于IL-2产生和反应性降低所致。

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