» Articles » PMID: 33668558

Refining Host-Pathogen Interactions: Organ-on-Chip Side of the Coin

Overview
Journal Pathogens
Date 2021 Mar 6
PMID 33668558
Citations 19
Authors
Affiliations
Soon will be listed here.
Abstract

Bioinspired organ-level in vitro platforms that recapitulate human organ physiology and organ-specific responses have emerged as effective technologies for infectious disease research, drug discovery, and personalized medicine. A major challenge in tissue engineering for infectious diseases has been the reconstruction of the dynamic 3D microenvironment reflecting the architectural and functional complexity of the human body in order to more accurately model the initiation and progression of host-microbe interactions. By bridging the gap between in vitro experimental models and human pathophysiology and providing alternatives for animal models, organ-on-chip microfluidic devices have so far been implemented in multiple research areas, contributing to major advances in the field. Given the emergence of the recent pandemic, plug-and-play organ chips may hold the key for tackling an unmet clinical need in the development of effective therapeutic strategies. In this review, latest studies harnessing organ-on-chip platforms to unravel host-pathogen interactions are presented to highlight the prospects for the microfluidic technology in infectious diseases research.

Citing Articles

Applying 3D cultures and high-throughput technologies to study host-pathogen interactions.

De Martinis E, Alves V, Pereira M, Andrade L, Abichabki N, Abramova A Front Immunol. 2025; 16:1488699.

PMID: 40051624 PMC: 11882522. DOI: 10.3389/fimmu.2025.1488699.


Centrifugal Microfluidic Cell Culture Platform for Physiologically Relevant Virus Infection Studies: A Case Study with HSV-1 Infection of Periodontal Cells.

Christfort J, Ortis M, Nguyen H, Marsault R, Doglio A Biosensors (Basel). 2024; 14(8).

PMID: 39194630 PMC: 11352947. DOI: 10.3390/bios14080401.


Developing organs-on-chips for biomedical applications.

Sun L, Chen H, Xu D, Liu R, Zhao Y Smart Med. 2024; 3(2):e20240009.

PMID: 39188702 PMC: 11236011. DOI: 10.1002/SMMD.20240009.


Small Animal Models to Study Herpes Simplex Virus Infections.

Hussain M, Stanfield B, Bernstein D Viruses. 2024; 16(7).

PMID: 39066200 PMC: 11281376. DOI: 10.3390/v16071037.


Vasculature-on-a-chip technologies as platforms for advanced studies of bacterial infections.

Gaudreau L, Stewart E Biomicrofluidics. 2024; 18(2):021503.

PMID: 38560344 PMC: 10977040. DOI: 10.1063/5.0179281.


References
1.
Jang K, Suh K . A multi-layer microfluidic device for efficient culture and analysis of renal tubular cells. Lab Chip. 2009; 10(1):36-42. DOI: 10.1039/b907515a. View

2.
Sunuwar L, Yin J, Kasendra M, Karalis K, Kaper J, Fleckenstein J . Mechanical Stimuli Affect Escherichia coli Heat-Stable Enterotoxin-Cyclic GMP Signaling in a Human Enteroid Intestine-Chip Model. Infect Immun. 2019; 88(3). PMC: 7035931. DOI: 10.1128/IAI.00866-19. View

3.
Booth R, Kim H . Characterization of a microfluidic in vitro model of the blood-brain barrier (μBBB). Lab Chip. 2012; 12(10):1784-92. DOI: 10.1039/c2lc40094d. View

4.
Ortega-Prieto A, Cherry C, Gunn H, Dorner M . In Vivo Model Systems for Hepatitis B Virus Research. ACS Infect Dis. 2018; 5(5):688-702. PMC: 6515358. DOI: 10.1021/acsinfecdis.8b00223. View

5.
Barr J . Missing a Phage: Unraveling Tripartite Symbioses within the Human Gut. mSystems. 2019; 4(3). PMC: 6533376. DOI: 10.1128/mSystems.00105-19. View