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与 SIVmac239 感染的北豚尾猴相比,较高的肠道完整性和有限的微生物易位与较低的免疫激活相关。

Superior intestinal integrity and limited microbial translocation are associated with lower immune activation in SIVmac239-infected northern pig-tailed macaques .

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, National Kunming High Level Biosafety Research Center for Non-human Primates, KIZ-CUHK Joint Laboratory of Bioresources and Molecular Research in Common Diseases, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming Yunnan 650223, China.

Kunming College of Life Science, University of Chinese Academy of Sciences, Kunming Yunnan 650204, China.

出版信息

Zool Res. 2019 Nov 18;40(6):522-531. doi: 10.24272/j.issn.2095-8137.2019.047.

Abstract

Microbial translocation is a cause of systemic immune activation in HIV/SIV infection. In the present study, we found a lower CD8 T cell activation level in (northern pig-tailed macaques, NPMs) than in (Chinese rhesus macaques, ChRMs) during SIVmac239 infection. Furthermore, the levels of plasma LPS-binding protein and soluble CD14 in NPMs were lower than those in ChRMs. Compared with ChRMs, SIV-infected NPMs had lower Chiu scores, representing relatively normal intestinal mucosa. In addition, no obvious damage to the ileum or colon epithelial barrier was observed in either infected or uninfected NPMs, which differed to that found in ChRMs. Furthermore, no significant microbial translocation ( ) was detected in the colon or ileum of infected or uninfected NPMs, which again differed to that observed in ChRMs. In conclusion, NPMs retained superior intestinal integrity and limited microbial translocation during SIV infection, which may contribute to their lower immune activation compared with ChRMs.

摘要

微生物易位是 HIV/SIV 感染导致全身免疫激活的一个原因。在本研究中,我们发现,在 SIVmac239 感染期间,(北方猪尾猕猴,NPMs)的 CD8 T 细胞活化水平低于(中国恒河猴,ChRMs)。此外,NPMs 中的血浆脂多糖结合蛋白和可溶性 CD14 水平低于 ChRMs。与 ChRMs 相比,感染 SIV 的 NPMs 的 Chiu 评分较低,代表其肠道黏膜相对正常。此外,无论是感染还是未感染的 NPMs,其回肠或结肠上皮屏障均未观察到明显的损伤,这与 ChRMs 的情况不同。此外,在感染或未感染的 NPMs 的结肠或回肠中均未检测到明显的微生物易位(),这与 ChRMs 的情况再次不同。总之,NPMs 在 SIV 感染期间保持了优异的肠道完整性和有限的微生物易位,这可能是它们与 ChRMs 相比免疫激活程度较低的原因。

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