Search bioRxiv⌕ Search

Biology subjects

Lanteri, C. A.

Publications and source records attributed to Lanteri, C. A..

2 recordsLinked to original sources

An Automated Method for the Assessment of Memory and Learning in Larval Zebrafish

Zebrafish have shown value in translational research for many human diseases, including neuropsychiatric disorders and cognitive dysfunction, with low cost and rapid testing facilitating drug screening and discovery. However, some endpoints, such as associative learning and long-term memory, have relied historically on manual data tracking that slows data acquisition and increases costs. We automated an associative learning/long-term memory test developed by Hinz et al.1 using a Noldus DanioVision system and EthoVision software to enhance assay throughput and utility for monitoring learning and memory behavior through automated tracking of location and movement of individual fish.

animal behavior and cognition↗

Durability of SARS-CoV-2-specific T cell responses at 12-months post-infection

BackgroundCharacterizing the longevity and quality of cellular immune responses to SARS-CoV-2 is critical to understanding immunologic approaches to protection against COVID-19. Prior studies suggest SARS-CoV-2-specific T cells are present in peripheral blood 10 months after infection. Further analysis of the function, durability, and diversity of the cellular response long after natural infection, over a wider range of ages and disease phenotypes, is needed to further identify preventative and therapeutic interventions. MethodsWe identified participants in our multi-site longitudinal, prospective cohort study 12-months post SARS-CoV-2 infection representing a range of disease severity. We investigated the function, phenotypes, and frequency of T cells specific for SARS-CoV-2 using intracellular cytokine staining and spectral flow cytometry. In parallel, the magnitude of SARS-CoV-2-specific antibodies was compared. ResultsSARS-CoV-2-specific antibodies and T cells were detected at 12-months post-infection. Severity of acute illness was associated with higher frequencies of SARS-CoV-2-specific CD4 T cells and antibodies at 12-months. In contrast, polyfunctional and cytotoxic T cells responsive to SARS-CoV-2 were identified in participants over a wide spectrum of disease severity. ConclusionsOur data show that SARS-CoV-2 infection induces polyfunctional memory T cells detectable at 12-months post-infection, with higher frequency noted in those who originally experienced severe disease.

immunology↗