THE CHALLENGE

When potency varies 100-fold between animal & cell lines, how confident can you be in your hit list?

Many antivirals, antibacterials or host-directed therapeutics fail in translation because they are evaluated in cell lines or animal models that do not recapitulate human tissue complexity, cell types, polarization, or multi-cell context. These models often lack 3D architecture, immune crosstalk or microbiome interactions, limiting predictive power for human efficacy or toxicity.
OUR SOLUTION

Patient-derived organoid platforms that capture the complexity of human infection

We deliver patient-derived organoid models and assays that capture tissue physiology, cellular heterogeneity, and microenvironmental interactions. We enable you to study infection, pathogen spread, drug effects, immune responses and barrier integrity, all in human-derived systems.

See the system in action!

Lung organoids demonstrating functional ciliated cells

PDO Monolayer Infection Models

PDO Monolayer Infection Models

A physiologically relevant human epithelial platform for infection and barrier studies

Our PDO Monolayers are engineered to faithfully recapitulate the composition of the epithelium in vivo, encompassing both stem cells and all differentiated lineages. This technology enables the culture of patient-derived biopsies from airway, intestinal, liver, or kidney tissues into uniform monolayers. The system is ideally suited for studies involving apical or basolateral infection routes, dose–response antiviral testing, cytotoxicity assessments, viral or bacterial replication analyses, and evaluations of barrier integrity.

CASE STUDY

Modeling viral infection in airway organoid monolayers

Our human airway organoid monolayers offer a powerful platform to study respiratory viruses like RSV and rhinovirus. They enable viral replication analysis, cytokine profiling, and live-cell imaging, while supporting antiviral dose–response testing and mechanistic insights into viral entry and spread – providing a complete toolkit for infection research.

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Co-culture for capturing host-pathogen interactions

Recapitulate immune, stromal or microbiome interactions during infection

Integrate immune cells, such as macrophages and T cells, as well as fibroblasts or endothelial elements, to capture host response dynamics. This approach enables modeling of microbiome–pathogen–host interactions, including commensal-mediated suppression of pathogens or dysbiosis-driven enhancement of infection. It also allows the study of immune evasion, cytokine storms, immunopathology, and drug modulation within a 3D patient biology context.

Want to know more?

ON-DEMAND WEBINAR

Modelling inflammation “in a dish”

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POSTER PRESENTATION

Patient-Derived Airway Organoids for Modelling Rhinovirus Infection

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PUBLICATION

Application of human liver organoids as a patient-derived primary model for HBV infection and related hepatocellular carcinoma

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