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一种基于多模态影像技术的呼吸道合胞病毒感染唐氏综合征小鼠模型。

A Multimodal Imaging-Supported Down Syndrome Mouse Model of RSV Infection.

机构信息

Biomedical MRI Unit/Mosaic, Department of Imaging and Pathology, KU Leuven, 3000 Leuven, Belgium.

Laboratory of Immunoparasitology, Department of Microbiology, Immunology and Transplantation, Rega Institute for Medical Research, KU Leuven, 3000 Leuven, Belgium.

出版信息

Viruses. 2023 Apr 18;15(4):993. doi: 10.3390/v15040993.

Abstract

Individuals with Down syndrome (DS) are more prone to develop severe respiratory tract infections. Although a RSV infection has a high clinical impact and severe outcome in individuals with DS, no vaccine nor effective therapeutics are available. Any research into infection pathophysiology or prophylactic and therapeutic antiviral strategies in the specific context of DS would greatly benefit this patient population, but currently such relevant animal models are lacking. This study aimed to develop and characterize the first mouse model of RSV infection in a DS-specific context. Ts65Dn mice and wild type littermates were inoculated with a bioluminescence imaging-enabled recombinant human RSV to longitudinally track viral replication in host cells throughout infection progression. This resulted in an active infection in the upper airways and lungs with similar viral load in Ts65Dn mice and euploid mice. Flow cytometric analysis of leukocytes in lungs and spleen demonstrated immune alterations with lower CD8+ T cells and B-cells in Ts65Dn mice. Overall, our study presents a novel DS-specific mouse model of hRSV infection and shows that potential in using the Ts65Dn preclinical model to study immune-specific responses of RSV in the context of DS and supports the need for models representing the pathological development.

摘要

唐氏综合征(DS)患者更容易发生严重的呼吸道感染。虽然呼吸道合胞病毒(RSV)感染在 DS 患者中具有较高的临床影响和严重的后果,但目前尚无有效的疫苗或治疗方法。任何针对 DS 特定背景下的感染发病机制或预防性和治疗性抗病毒策略的研究都将极大地有益于这一患者群体,但目前缺乏相关的动物模型。本研究旨在开发和表征第一个在 DS 特定背景下的 RSV 感染小鼠模型。Ts65Dn 小鼠和野生型同窝仔鼠接种了可进行生物发光成像的重组人 RSV,以在整个感染过程中对宿主细胞中的病毒复制进行纵向跟踪。结果显示,在上呼吸道和肺部中引起了活跃的感染,Ts65Dn 小鼠和正常二倍体小鼠的病毒载量相似。对肺部和脾脏白细胞的流式细胞分析表明,Ts65Dn 小鼠的 CD8+T 细胞和 B 细胞数量减少,存在免疫改变。总之,本研究提出了一种新的针对 hRSV 感染的 DS 特异性小鼠模型,并表明 Ts65Dn 临床前模型在研究 DS 背景下 RSV 的免疫特异性反应方面具有潜力,并支持需要建立能够代表疾病发展的模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c937/10144178/f0b506f66972/viruses-15-00993-g001.jpg

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