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Published on: November 3, 2012
In vitro and ex vivo models of microbial keratitis: Present and future
Kelvin Kah Wai Cheng1, Leonie Fingerhut1, Sheelagh Duncan1
1Centre for Inflammation Research, Institute of Regeneration and Repair, University of Edinburgh, United Kingdom.
Abstract:
Microbial keratitis (MK) is an infection of the cornea, caused by bacteria, fungi, parasites, or viruses. MK leads to significant morbidity, being the fifth leading cause of blindness worldwide. There is an urgent requirement to better understand pathogenesis in order to develop novel diagnostic and therapeutic approaches to improve patient outcomes. Many in vitro, ex vivo and in vivo MK models have been developed and implemented to meet this aim. Here, we present current in vitro and ex vivo MK model systems, examining their varied design, outputs, reporting standards, and strengths and limitations. Major limitations include their relative simplicity and the perceived inability to study the immune response in these MK models, an aspect widely accepted to play a significant role in MK pathogenesis. Consequently, there remains a dependence on in vivo models to study this aspect of MK. However, looking to the future, we draw from the broader field of corneal disease modelling, which utilises, for example, three-dimensional co-culture models and dynamic environments observed in bioreactors and organ-on-a-chip scenarios. These remain unexplored in MK research, but incorporation of these approaches will offer further advances in the field of MK corneal modelling, in particular with the focus of incorporation of immune components which we anticipate will better recapitulate pathogenesis and yield novel findings, therefore contributing to the enhancement of MK outcomes.
Insights
Microbial keratitis (MK) models are crucial for understanding corneal infection. Current in vitro and ex vivo models have limitations, particularly in studying the immune response, necessitating future advancements in corneal disease modeling.
Area of Science:
- Ophthalmology and Microbiology
- Corneal disease modeling
Background:
- Microbial keratitis (MK) is a major cause of blindness worldwide.
- Understanding MK pathogenesis is vital for developing new diagnostics and therapeutics.
- Existing MK models are essential but have limitations.
Purpose of the Study:
- To review current in vitro and ex vivo microbial keratitis (MK) models.
- To examine their designs, outputs, standards, strengths, and limitations.
- To explore future directions for MK modeling.
Main Methods:
- Review of existing in vitro and ex vivo microbial keratitis (MK) models.
- Analysis of model designs, outputs, reporting standards, strengths, and limitations.
- Exploration of advanced modeling techniques from other corneal disease research.
Main Results:
- Current in vitro and ex vivo MK models are valuable but limited in scope.
- A significant limitation is the inability to adequately study the immune response in MK.
- In vivo models are still relied upon for studying immune aspects of MK pathogenesis.
Conclusions:
- Advanced modeling approaches like 3D co-cultures and organ-on-a-chip systems hold promise for MK research.
- Incorporating immune components into future MK models is anticipated to improve pathogenesis recapitulation.
- Novel findings from improved MK models could lead to better patient outcomes.
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