[HTML][HTML] Single-cell RNA-Seq revealed profound immune alteration in the peripheral blood of patients with bacterial infection
H Lei, C Wang, Y Wang, C Wang - International Journal of Infectious …, 2021 - Elsevier
H Lei, C Wang, Y Wang, C Wang
International Journal of Infectious Diseases, 2021•ElsevierObjectives Bacterial infection remains one of the greatest threats to human health. However,
how human hosts respond to bacterial infection has not been thoroughly understood. Better
understanding of this response will improve human health. Methods Here, we conducted an
investigation on host response to bacterial infection using unperturbed clinical samples and
single-cell RNA-Seq (scRNA-Seq) technology. To evaluate immune alteration upon
bacterial infection in scRNA-Seq data of peripheral blood mononuclear cells (PBMCs), we …
how human hosts respond to bacterial infection has not been thoroughly understood. Better
understanding of this response will improve human health. Methods Here, we conducted an
investigation on host response to bacterial infection using unperturbed clinical samples and
single-cell RNA-Seq (scRNA-Seq) technology. To evaluate immune alteration upon
bacterial infection in scRNA-Seq data of peripheral blood mononuclear cells (PBMCs), we …
Objectives
Bacterial infection remains one of the greatest threats to human health. However, how human hosts respond to bacterial infection has not been thoroughly understood. Better understanding of this response will improve human health.
Methods
Here, we conducted an investigation on host response to bacterial infection using unperturbed clinical samples and single-cell RNA-Seq (scRNA-Seq) technology. To evaluate immune alteration upon bacterial infection in scRNA-Seq data of peripheral blood mononuclear cells (PBMCs), we developed a barcode analytical framework named PBMCode.
Results
Using this PBMCode framework, we revealed profound immune alteration in peripheral blood under bacterial infection, including the emergence of natural killer T (NKT) cell cluster, reduction of B cell population, and considerable changes in T cells and monocytes. In addition, we also observed a large quantity of low-density neutrophils.
Conclusions
Our investigation on single cells provided unprecedented details in the alteration of both cell population and cell state under bacterial infection. These findings may be relevant to clinical decisions. The complexity of host response to bacterial infection revealed by scRNA-Seq deserves further attention in future studies.
Elsevier
