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DOI 10.21769/bioprotoc.5230

Медицинская библиотека · Bio-protocol · 2025

Protocol for Screening Host-Targeting Antivirals (HTAs) Using Human PBMCs and pDCs.

Low Zhao Xuan, Kanauchi Osamu, AbuBakar Sazaly, Tiong Vunjia, Hassandarvish Pouya

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Аннотация

This protocol offers an ex vivo method for screening host-targeting antivirals (HTAs) using human peripheral blood mononuclear cells (PBMCs) or plasmacytoid dendritic cells (pDCs). Unlike virus-targeting antivirals (VTAs), HTAs provide advantages in overcoming drug resistance and offering broad-spectrum protection, especially against rapidly mutating or newly emerging viruses. By focusing on PBMCs or pDCs, known for their high production of humoral factors such as Type I interferons (IFNs), the protocol enables the screening of antivirals that modulate immune responses against viruses. Targeting host pathways, especially innate immunity, allows for species-independent antiviral activity, reducing the likelihood of viral escape mutations. Additionally, the protocol's versatility makes it a powerful tool for testing potential antivirals against various viral pathogens, including emerging viruses, positioning it as an essential resource in both pandemic preparedness and broad-spectrum antiviral research. This approach differentiates itself from existing protocols by focusing on host immune modulation through pDCs, offering a novel avenue for HTA discovery. Key features • Optimized protocol for screening HTAs against dengue virus (DENV), chikungunya virus (CHIKV), and Zika virus (ZIKV). • This protocol is ideal for screening soluble or intravenous-formulated compounds for evaluating their efficacy in experimental settings. • This protocol builds upon the method developed by Tsuji et al. [1] and extends its application to PBMCs and testing against DENV, CHIKV, and ZIKV.

Для цитирования: Low Zhao Xuan, Kanauchi Osamu, AbuBakar Sazaly, Tiong Vunjia, Hassandarvish Pouya. Protocol for Screening Host-Targeting Antivirals (HTAs) Using Human PBMCs and pDCs.. Bio-protocol. 2025. DOI: 10.21769/bioprotoc.5230.
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