Key result
Spatial transcriptomics reveals localized immune responses and pathways driving human coronary atherosclerosis pathogenesis.
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Spatial transcriptomics provides a powerful tool to elucidate localized immune responses and identify novel therapeutic targets in human atherosclerotic coronary arteries at the single-cell level.
Atherosclerosis is characterized by the accumulation of lipids and immune cells in the arterial wall, leading to the narrowing and stiffening of blood vessels. Innate and adaptive immunity are involved in the pathogenesis of human atherosclerosis. However, spatial organization and roles of immune cells during disease progression remain poorly understood. A better understanding of the immune response's contribution to atherosclerosis progression could unveil novel therapeutic targets to mitigate plaque development and rupture, ultimately reducing cardiovascular events burden. Here, we utilised GeoMx® and CosMx™ technologies to analyse serial sections of human coronary arteries from patients with varying degrees of atherosclerotic lesion severity. Our work comprises a series of investigations and integrates findings from both datasets, including pathway analyses, cell typing, and neighbourhood analysis. This workflow highlights the power of combining these spatial transcriptomics platforms to elucidate biological processes at the single-cell level. Our approach unbiasedly identifies molecules and pathways of relevance to support the understanding of atherosclerosis pathogenesis and assess the potential for novel therapies.
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Campos et al. (2025) studied Atherosclerosis. Spatial transcriptomics (GeoMx and CosMx technologies) was evaluated. Spatial transcriptomics using GeoMx and CosMx technologies on human coronary arteries identified localized immune responses and pathways relevant to atherosclerosis pathogenesis.
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