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Daniel Caron

As seen in: UOL, Nature, MDPI, Science Magazine, BioRxiv, Cell Press, Ottawa Citizen, i24NEWS, The Tufts Daily, Policy Options Politiques Magazine and
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Articles

Distinct transcription factors control tissue adaptation and effector function in infant and adult memory T cells

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By Peter A. Szabo, Péter Szabó, Hanna M Levitin, Siddhi Nargund, Thomas Connors, David Chen, Jenny Jin Verified, Puspa Thapa, Rebecca Guyer, Daniel Caron, Joshua Gray, Rei Matsumoto, Masaru Kubota, Maigan Brusko, Todd M. Brusko, Donna L Farber, Peter Sims
| Nature Verified
Abstract Early life is essential for establishing memory T cells, which rapidly populate mucosal sites during infancy, although these nascent memory T cells are less protective than their adult counterparts. Here we used single-cell RNA sequencing of resting and CD3+CD28 antibody-stimulated T cells from lymphoid and mucosal tissues of infant (2–9 months) and adult (40–63 years) organ donors to investigate age-dependent mechanisms for functional regulation of human memory T cells.
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Multimodal profiling reveals tissue-directed signatures of human immune cells altered with age - Nature Immunology

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By Steven Wells, Daniel B Rainbow, Peter A. Szabo, Péter Szabó, Can Ergen, Daniel Caron, Ana Raquel Maceiras, David Chen Verified, Allon Wagner, Lorna B. Jarvis, Krishnaa T. Mahbubani, Laura Richardson, Chuan Xu, Sarah A Teichmann, Donna L Farber, Peter Sims, Joanne Jones, Kouresh Saeb-Parsy
| Nature Verified
Abstract The immune system comprises multiple cell lineages and subsets maintained in tissues throughout the lifespan, with unknown effects of tissue and age on immune cell function. Here we comprehensively profiled RNA and surface protein expression of over 1.25 million immune cells from blood and lymphoid and mucosal tissues from 24 organ donors aged 20–75 years.
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Tissue signatures of human macrophages during homeostasis and activation

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By Daniel Caron, William L Specht, David Chen Verified, Steven Wells
| BioRxiv
Abstract Human macrophages (MΦs) reside in tissues and develop tissue-specific identities. While studies in mice have identified molecular signatures for site-specific MΦ differentiation, we know less about the transcriptional profiles of human MΦs in distinct sites, including mucosal tissues and lymphoid organs during homeostasis and activation.
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