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Organoid Models in Host–Pathogen Interactions and Disease Pathogenesis

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Molecular Biology".

Deadline for manuscript submissions: 20 June 2026 | Viewed by 1365

Special Issue Editor

Special Issue Information

Dear Colleagues,

This Special Issue aims to highlight recent advances in the use of organoid technology to study the pathogenesis of infectious diseases. Organoids, three-dimensional and self-organizing structures derived from stem cells, offer physiologically relevant platforms that closely mimic the architecture and cellular diversity of human tissues. These models have transformed our ability to investigate host–pathogen interactions at mucosal surfaces, in deep tissues, and within immune-privileged sites, providing insights unattainable with traditional 2D cultures or animal models. We welcome original research articles, reviews, and methods papers focused on how organoid systems are being applied to model bacterial, viral, fungal, and parasitic infections. Topics of interest include organoid-based studies of microbial invasion, immune response, tissue injury and repair, microbiota interactions, and antimicrobial or vaccine testing. Studies that integrate immune cells, use organoid-on-a-chip platforms, or develop multi-organoid co-cultures are particularly encouraged.

Through this collection, we aim to advance the understanding of human disease mechanisms and promote the development of more predictive models for translational research.

Dr. Apichai Tuanyok
Guest Editor

Manuscript Submission Information

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Keywords

  • organoids
  • host–pathogen interaction
  • infectious disease models
  • mucosal immunity
  • tissue engineering
  • microbial pathogenesis
  • immune organoids
  • 3D culture systems

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Published Papers (1 paper)

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Research

28 pages, 6020 KB  
Article
Development of a High-Throughput Screening Platform and a Pathogenesis Model for Leishmania Infection Based on Mouse Hepatic Organoids
by María-Cristina González-Montero, Julia Andrés-Rodríguez, Miguel Criado, Sonia Andrés, Giulio Galli, Celia Fernández-Rubio, Yolanda Pérez-Pertejo, Rosa M. Reguera, Rafael Balaña-Fouce and Carlos García-Estrada
Int. J. Mol. Sci. 2025, 26(24), 12180; https://doi.org/10.3390/ijms262412180 - 18 Dec 2025
Viewed by 867
Abstract
The development of new alternative models is essential to overcome the limitations of traditional two-dimensional (2D) cell cultures and animal models. Three-dimensional (3D) models, such as organoids, better mimic the structural and functional complexity of mammalian organs, thereby reducing the ethical and economic [...] Read more.
The development of new alternative models is essential to overcome the limitations of traditional two-dimensional (2D) cell cultures and animal models. Three-dimensional (3D) models, such as organoids, better mimic the structural and functional complexity of mammalian organs, thereby reducing the ethical and economic issues related to animal experimentation. These systems provide more physiologically relevant environments, improving the accuracy of disease modeling and drug response prediction. In this context, we have developed mouse hepatic organoids from livers of adult BALB/c mice and characterized them by microscopy and transcriptional analysis. This model was applied to a robust and reproducible high-throughput screening (HTS) platform for testing cytotoxicity at the preclinical stage of drug discovery. In addition, mouse hepatic organoids were co-cultured with amastigotes of Leishmania donovani parasites to establish a model of host–parasite interaction, which was characterized by RNA-seq linked to differential expression analysis and cytokine production by the hepatic organoids. The findings provided in this work establish mouse hepatic organoids as an alternative model for drug discovery and pathogenesis studies. Full article
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