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宋天章, 张明旭, 夏玉洁, 肖裕, 庞伟, 郑永唐. 2018: 寄生虫逃避免疫功能不全宿主. 动物学研究, 39(1): 42-51. DOI: 10.24272/j.issn.2095-8137.2018.015
引用本文: 宋天章, 张明旭, 夏玉洁, 肖裕, 庞伟, 郑永唐. 2018: 寄生虫逃避免疫功能不全宿主. 动物学研究, 39(1): 42-51. DOI: 10.24272/j.issn.2095-8137.2018.015
Tian-Zhang Song, Ming-Xu Zhang, Yu-Jie Xia, Yu Xiao, Wei Pang, Yong-Tang Zheng. 2018. Parasites may exit immunocompromised northern pig-tailed macaques (Macaca leonina) infected with SIVmac239. Zoological Research, 39(1): 42-51. DOI: 10.24272/j.issn.2095-8137.2018.015
Citation: Tian-Zhang Song, Ming-Xu Zhang, Yu-Jie Xia, Yu Xiao, Wei Pang, Yong-Tang Zheng. 2018. Parasites may exit immunocompromised northern pig-tailed macaques (Macaca leonina) infected with SIVmac239. Zoological Research, 39(1): 42-51. DOI: 10.24272/j.issn.2095-8137.2018.015

寄生虫逃避免疫功能不全宿主

Parasites may exit immunocompromised northern pig-tailed macaques (Macaca leonina) infected with SIVmac239

  • 摘要: 以往认为,HIV感染者寄生虫感染率明显高于普通人群。然而,近年来部分体外实验及流行病学研究显示,寄生虫有逃避免疫功能不全HIV感染者的趋势。由于缺乏直接动物实验证据,因此,寄生虫与免疫功能不全宿主的关系仍然不清。本实验中,在SIV感染之前及感染后第50周,对6只北平顶猴进行14种寄生虫感染情况的检测。结果显示,SIV感染之前,6只北平顶猴均检测到多种寄生虫感染。感染后第50周,08247及08287未发现寄生虫感染(Parasites Exit, PE)。09203,09211,10205和10225仍保留部分寄生虫感染(Parasites Remain,PR)。与PR组相比,PE组实验动物具有更高的SIV病毒载量,更低的CD4+ T细胞数量及CD4/CD8 T细胞比例。此外,PE组CD4+ T细胞与CD8+ T细胞表现出更明显的活化及耗竭。病理学检测发现PE组在肝脏,盲肠,结肠,脾脏和肠系膜淋巴结均存在明显的病理损伤。因此,PE组实验动物表现为更严重的免疫功能不全。与PR组相比,免疫功能不全宿主发生了寄生虫逃避现象。

     

    Abstract: Parasites can increase infection rates andpathogenicity in immunocompromised humanimmunodeficiency virus (HIV) patients. However, invitro studies and epidemiological investigationsalso suggest that parasites might escapeimmunocompromised hosts during HIV infection.Due to the lack of direct evidence from animalexperiments, the effects of parasitic infections onimmunocompromised hosts remain unclear. Here,we detected 14 different parasites in six northernpig-tailed macaques (NPMs) before or during the50th week of post-simian immunodeficiency virus(SIV) infection by ELISA. The NPMs all carriedparasites before viral injection. At the 50th week afterviral injection, the individuals with negative resultsin parasitic detection (i.e., 08247 and 08287) werecharacterized as the Parasites Exit (PE) group, withthe other individuals (i.e., 09203, 09211, 10205, and10225) characterized as the Parasites Remain (PR)group. Compared with the PR group, the NPMs in thePE group showed higher viral loads, lower CD4+ Tcells counts, and lower CD4/CD8 rates. Additionally,the PE group had higher immune activation andimmune exhaustion of both CD4+ and CD8+ T cells.Pathological observation showed greater injury tothe liver, cecum, colon, spleen, and mesentericlymph nodes in the PE group. This study showedmore seriously compromised immunity in the PEgroup, strongly indicating that parasites might exit animmunocompromised host.

     

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