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Assessing the Innate Sensing of HIV-1 Infected CD4+ T Cells by Plasmacytoid Dendritic Cells Using an Ex vivo Co-culture System.
Published on: September 1, 2015
TLR4 sensitizes plasmacytoid dendritic cells for antiviral response against SARS-CoV-2 coronavirus
King Hoo Lim1, Lishi Wang2, Eunice Dotse1
1Department of Biomedical Sciences, City University of Hong Kong, 83 Tat Chee Ave, Kowloon Tong, Kowloon, Hong Kong.
Abstract:
Plasmacytoid dendritic cells are a rare subset of dendritic cells that exhibit antiviral functions in response to toll-like receptor 7/8 stimulations. Alternative toll-like receptors such as TLR4 have been known to be active in plasmacytoid dendritic cells for immune regulatory functions. However, it is unclear whether these toll-like receptors differentially activate plasmacytoid dendritic cells as compared with canonical toll-like receptor 7/8 stimulation. Here, we assessed alternative plasmacytoid dendritic cell activation states mediated by toll-like receptors other than endosomal toll-like receptors via the RNA sequencing approach. We found that toll-like receptor 4 stimulation induced a high degree of similarity in gene expression pattern to toll-like receptor 7/8 stimulation in plasmacytoid dendritic cells. Despite high resemblance to toll-like receptor 7/8, we discovered unique genes that were activated under toll-like receptor 4 activation only, as well as genes that were induced at a higher magnitude in comparison to toll-like receptor 7/8 activation. In comparison between toll-like receptor 4-activated plasmacytoid dendritic cells and conventional dendritic cells, we revealed that plasmacytoid dendritic cells and conventional dendritic cells expressed distinct gene sets, whereby conventional dendritic cells mostly favored antigen presentation functions for adaptive immune response regulation while plasmacytoid dendritic cells leaned toward immune response against infectious diseases. Last, we determined that toll-like receptor 4 activation sensitized plasmacytoid dendritic cells against SARS-CoV-2 (COVID-19) single-stranded RNA by enhancing antiviral-related responses and type I interferon production. These findings provided greater insights into the toll-like receptor 4 activation state in plasmacytoid dendritic cells, which can be beneficial for alternative therapeutic interventions involving plasmacytoid dendritic cells for various diseases.
Insights
Toll-like receptor 4 (TLR4) activates plasmacytoid dendritic cells similarly to TLR7/8, enhancing antiviral responses and type I interferon production against SARS-CoV-2. This reveals unique TLR4 activation pathways for therapeutic potential.
Area of Science:
- Immunology
- Cell Biology
Background:
- Plasmacytoid dendritic cells (pDCs) are crucial for antiviral immunity, primarily via Toll-like receptor 7/8 (TLR7/8) stimulation.
- The role of alternative Toll-like receptors (TLRs), such as TLR4, in pDC activation remains less understood compared to endosomal TLRs.
Purpose of the Study:
- To investigate and compare pDC activation states induced by TLR4 stimulation versus canonical TLR7/8 stimulation.
- To identify unique gene expression profiles and functional responses of pDCs under TLR4 activation.
Main Methods:
- RNA sequencing was employed to analyze gene expression patterns in pDCs stimulated with TLR4 agonists.
- Comparative analysis of gene expression between TLR4-activated pDCs, TLR7/8-activated pDCs, and conventional dendritic cells (cDCs).
Main Results:
- TLR4 stimulation induced gene expression patterns highly similar to TLR7/8 stimulation in pDCs.
- Unique genes were identified under TLR4 activation, and some genes showed higher induction magnitude compared to TLR7/8.
- TLR4-activated pDCs exhibited distinct gene sets from cDCs, favoring infectious disease response over antigen presentation.
- TLR4 activation sensitized pDCs against SARS-CoV-2 RNA by enhancing antiviral responses and type I interferon production.
Conclusions:
- TLR4 activation represents a significant pathway for pDC activation, sharing similarities but also possessing unique characteristics compared to TLR7/8.
- TLR4-mediated pDC activation enhances antiviral immunity, particularly against SARS-CoV-2, through type I interferon induction.
- Understanding TLR4-driven pDC responses offers potential for novel therapeutic strategies in infectious diseases and other conditions.
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