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免疫功能低下的感染 SIVmac239 的北部长尾猕猴 () 可能会排出寄生虫。

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

机构信息

Key Laboratory of Animal Models and Human Disease Mechanisms of the Chinese Academy of Sciences/Key Laboratory of Bioactive Peptides of Yunnan Province, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming Yunnan 650223, China.

University of Chinese Academy of Sciences, Beijing 100049, China.

出版信息

Zool Res. 2018 Jan 18;39(1):42-51. doi: 10.24272/j.issn.2095-8137.2018.015.

Abstract

Parasites can increase infection rates and pathogenicity in immunocompromised human immunodeficiency virus (HIV) patients. However, studies and epidemiological investigations also suggest that parasites might escape immunocompromised hosts during HIV infection. Due to the lack of direct evidence from animal experiments, the effects of parasitic infections on immunocompromised hosts remain unclear. Here, we detected 14 different parasites in six northern pig-tailed macaques (NPMs) before or at the 50th week of simian immunodeficiency virus (SIV) infection by ELISA. The NPMs all carried parasites before viral injection. At the 50th week after viral injection, the individuals with negative results in parasitic detection (i.e., 08247 and 08287) were characterized as the Parasites Exit (PE) group, with the other individuals (i.e., 09203, 09211, 10205, and 10225) characterized as the Parasites Remain (PR) group. Compared with the PR group, the NPMs in the PE group showed higher viral loads, lower CD4 T cells counts, and lower CD4/CD8 rates. Additionally, the PE group had higher immune activation and immune exhaustion of both CD4 and CD8 T cells. Pathological observation showed greater injury to the liver, cecum, colon, spleen, and mesenteric lymph nodes in the PE group. This study showed more seriously compromised immunity in the PE group, strongly indicating that parasites might exit an immunocompromised host.

摘要

寄生虫可增加免疫功能低下人类免疫缺陷病毒(HIV)患者的感染率和致病性。然而,研究和流行病学调查也表明,寄生虫可能在 HIV 感染期间逃避免疫功能低下宿主。由于缺乏来自动物实验的直接证据,寄生虫感染对免疫功能低下宿主的影响仍不清楚。在这里,我们通过 ELISA 在 6 只北方长尾猕猴(NPM)感染 SIV 的第 50 周之前或此时检测到 14 种不同的寄生虫。在病毒注射之前,所有 NPM 都携带寄生虫。在病毒注射后的第 50 周,寄生虫检测结果为阴性的个体(即 08247 和 08287)被归类为寄生虫排出(PE)组,而其他个体(即 09203、09211、10205 和 10225)被归类为寄生虫残留(PR)组。与 PR 组相比,PE 组的 NPM 具有更高的病毒载量、更低的 CD4 T 细胞计数和更低的 CD4/CD8 比率。此外,PE 组的 CD4 和 CD8 T 细胞的免疫激活和免疫耗竭更高。病理观察显示,PE 组的肝脏、盲肠、结肠、脾脏和肠系膜淋巴结损伤更大。本研究表明,PE 组的免疫功能受到更严重的损害,强烈表明寄生虫可能从免疫功能低下的宿主中排出。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84e3/5869241/c782c3792fca/ZoolRes-39-1-42-g001.jpg

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