利用微生理系统加快对宿主-寄生虫相互作用的理解。

IF 5.5 1区 医学 Q1 MICROBIOLOGY
PLoS Pathogens Pub Date : 2025-04-24 eCollection Date: 2025-04-01 DOI:10.1371/journal.ppat.1013088
Maria Zorrinho-Almeida, Jorge de-Carvalho, Maria Bernabeu, Sara Silva Pereira
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引用次数: 0

摘要

微生理系统(MPS)复制细胞、组织和流体之间的动态相互作用。它们已经成为生物学的变革工具,并越来越多地应用于宿主-寄生虫的相互作用。与传统的体外模型相比,MPS可以更好地代表细胞行为,有助于研究寄生虫的趋向性、免疫逃避和各种寄生虫疾病的生命周期转变。应用跨越多种宿主组织和病原体,利用先进的生物工程和微加工技术来解决长期存在的知识空白。在这里,我们回顾了MPS应用于寄生虫病的最新进展,并确定了持续存在的挑战和投资机会。通过完善这些系统并整合宿主多细胞模型和寄生虫,MPS具有彻底改变寄生虫学的巨大潜力,通过更深入的机制理解和有针对性的干预措施增强我们对抗寄生虫病的能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Leveraging microphysiological systems to expedite understanding of host-parasite interactions.

Microphysiological systems (MPS) replicate the dynamic interactions between cells, tissues, and fluids. They have emerged as transformative tools for biology and have been increasingly applied to host-parasite interactions. Offering a better representation of cellular behavior compared with traditional in vitro models, MPS can facilitate the study of parasite tropism, immune evasion, and life cycle transitions across diverse parasitic diseases. Applications span multiple host tissues and pathogens, leveraging advanced bioengineering and microfabrication techniques to address long-standing knowledge gaps. Here, we review recent advances in MPS applied to parasitic diseases and identify persisting challenges and opportunities for investment. By refining these systems and integrating host multicellular models and parasites, MPS hold vast potential to revolutionize parasitology, enhancing our ability to combat parasitic diseases through deeper mechanistic understanding and targeted interventions.

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来源期刊
PLoS Pathogens
PLoS Pathogens MICROBIOLOGY-PARASITOLOGY
自引率
3.00%
发文量
598
期刊介绍: Bacteria, fungi, parasites, prions and viruses cause a plethora of diseases that have important medical, agricultural, and economic consequences. Moreover, the study of microbes continues to provide novel insights into such fundamental processes as the molecular basis of cellular and organismal function.
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