New study on tongue tissue sheds light on spatial regulation of inflammatory response in COVID-19 patients.
Study on spatial multiomic analysis of tongue tissue from COVID-19 patients reveals new insights to understand cell-type-specific and spatial regulation of inflammatory response in COVID-19 patients. It was presented at the 52nd Annual Meeting & Exhibition of the AADOCR, held in conjunction with the 47th Annual Meeting of the CADR. The AADOCR/CADR Annual Meeting & Exhibition took place at the Oregon Convention Center in Portland on March 15-18, 2023.
‘New study uncovers cell-specific inflammatory response in COVID-19 patients through tongue tissue analysis.’
This research was presented as part of the Interactive Talk presentation, “Oral Niches Self-Direct Distinct Immune Cues During SARS-CoV-2 Infection”. The study, led by Kevin M. Byrd of the ADA Science & Research Institute, performed autopsies on control and COVID-19 subjects (ETHICS APPROVAL 30364720.0.0000.0068); SARS-CoV-2 was confirmed by PCR.
A panel of 43 mucosal, stromal, vasculature and immune markers was optimized for highly-multiplexed immunohistochemistry (Phenocycler-Fusion) combined with in-situ hybridization (RNAscope). Images were segmented (QuPath) and phenotyped using manual, automated, and unsupervised methods.
Cell neighborhood analyses were performed using k-nearest-neighbors (NeighborhoodCoordination). Tissue and ROI spatial “rulesets” were analyzed between healthy and COVID-19-matched tissues and across tissues to understand niche-specific immune responses to acute COVID-19.
New Insights Into COVID-19 Inflammatory Response Revealed!
The study found that seven of ten taste papillae from COVID-19 autopsies harbored SARS-CoV-2 in the barrier epithelia; the majority displayed neural degeneration and mild to moderate inflammation. Salivary glands also displayed mild to moderate inflammation, with a shift to adaptive immune responses resulting in sialadenitis.Advertisement
Immune profile complexity and adaptive immune profiles by niche were directly influenced by time since diagnosis and local infection/replication burden.
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Source-Eurekalert