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• W4386002246 abstract "Respiratory infections caused by coronaviruses (CoVs) have become a major public health concern in the past two decades as revealed by the emergence of SARS-CoV in 2002, MERS-CoV in 2012, and SARS-CoV-2 in 2019. The most severe clinical phenotypes commonly arise from exacerbation of immune response following the infection of alveolar epithelial cells localized at the pulmonary blood-air barrier. Preclinical rodent models do not adequately represent the essential genetic properties of the barrier, thus necessitating the use of humanized transgenic models. However, existing monolayer cell culture models have so far been unable to mimic the complex lung microenvironment. In this respect, air–liquid interface models, tissue engineered models, and organ-on-a-chip systems, which aim to better imitate the infection site microenvironment and microphysiology, are being developed to replace the commonly used monolayer cell culture models, and their use is becoming more widespread every day. On the contrary, studies on the development of nanoparticles (NPs) that mimic respiratory viruses, and those NPs used in therapy are progressing rapidly. The first part of this review describes in vitro models that mimic the blood-air barrier, the tissue interface that plays a central role in COVID-19 progression. In the second part of the review, NPs mimicking the virus and/or designed to carry therapeutic agents are explained and exemplified. COVID-19 pandemic highlighted the urgent need to gain a deeper understanding of viral infection pathogenesis and develop approaches for rapid translation of research findings as vaccines or therapeutics that will protect the public from future pandemics. Numerous studies are in progress worldwide but advanced in vitro models that accurately mimic the natural microenvironment of the infection site are still under development. This review aims to introduce a brief summary of the features of the models currently used and that need to be improved, especially for researchers working in the field of regenerative medicine and nanotechnology." @default.
• W4386002246 created "2023-08-20" @default.
• W4386002246 creator A5004346273 @default.
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• W4386002246 date "2023-09-26" @default.
• W4386002246 modified "2023-10-14" @default.
• W4386002246 title "Advances in <i>In Vitro</i> Blood-Air Barrier Models and the Use of Nanoparticles in COVID-19 Research" @default.
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