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比较全血和脾转录特征在实验性疟疾感染过程中的变化。

Comparison of whole blood and spleen transcriptional signatures over the course of an experimental malaria infection.

机构信息

The Francis Crick Institute, London, United Kingdom.

West African Centre for Cell Biology of Infectious Pathogens, University of Ghana, Accra, Ghana.

出版信息

Sci Rep. 2019 Nov 1;9(1):15853. doi: 10.1038/s41598-019-52388-y.

Abstract

Although the spleen is broadly accepted as the major lymphoid organ involved in generating immune responses to the erythrocytic stages of the malaria parasite, Plasmodium, human splenic tissue is not readily available in most cases. As a result, most studies of malaria in humans rely on peripheral blood to assess cellular immune responses to malaria. The suitability of peripheral blood as a proxy for splenic immune responses is however unknown. Here, we have simultaneously analysed the transcriptomes of whole blood and spleen over 12 days of erythrocytic stage Plasmodium chabaudi infection in C57BL/6 mice. Using both unsupervised and directed approaches, we compared gene expression between blood and spleen over the course of infection. Taking advantage of publicly available datasets, we used machine learning approaches to infer cell proportions and cell-specific gene expression signatures from our whole tissue transcriptome data. Our findings demonstrate that spleen and blood are quite dissimilar, sharing only a small amount of transcriptional information between them, with transcriptional differences in both cellular composition and transcriptional activity. These results suggest that while blood transcriptome data may be useful in defining surrogate markers of protection and pathology, they should not be used to predict specific immune responses occurring in lymphoid organs.

摘要

虽然脾脏被广泛认为是参与产生对疟原虫红细胞阶段免疫反应的主要淋巴器官,但在大多数情况下,人类脾组织不易获得。因此,大多数关于人类疟疾的研究依赖于外周血来评估对疟疾的细胞免疫反应。然而,外周血作为脾免疫反应的替代物的适宜性尚不清楚。在这里,我们在 C57BL/6 小鼠感染红细胞期疟原虫 chabaudi 的 12 天内,同时分析了全血和脾脏的转录组。我们使用无监督和有监督的方法,比较了感染过程中血液和脾脏之间的基因表达。利用公开可用的数据集,我们使用机器学习方法从我们的整个组织转录组数据中推断细胞比例和细胞特异性基因表达特征。我们的研究结果表明,脾脏和血液之间存在很大的差异,它们之间只共享少量的转录信息,细胞组成和转录活性都存在转录差异。这些结果表明,虽然血液转录组数据可能有助于定义保护和病理的替代标志物,但不应将其用于预测发生在淋巴器官中的特定免疫反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16bf/6825210/1e56a2b465fd/41598_2019_52388_Fig1_HTML.jpg

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