Memory T cell subsets, migration patterns, and tissue residence.

By Scott N. Mueller, T. Gebhardt, F. Carbone, W. Heath. Annual Review of Immunology, 2013

808 citations recorded by the source corpus.

View Paper: https://www.semanticscholar.org/paper/9ff547883d14ce79c0c34dfe98f61935f642d7a9

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In Immunology

Citations in the corpus

Dendritic-cell-based therapeutic cancer vaccines. (2013, background): “A third category, i.e., tissue-resident memory T cells, has been recently identified (Jiang et al., 2012;Mueller et al., 2013) and shown to be superior to circulating memory T cells at providing rapid long-term protection against reinfection (Gebhardt et al., 2009; Jiang et al., 2012).”
Engineering T cells with Customized Therapeutic Response Programs Using Synthetic Notch Receptors (2016, neutral): “T cells also have the capacity to generate long-lived memory to disease, in principle, preventing recurrence over the course of years or a lifetime (Kalos et al., 2011; Maus et al., 2014; Mueller et al., 2013).”
Quantifying memory CD8 T cells reveals regionalization of immunosurveillance (2015, background): “It recently became clear that a third subset, termed tissue resident memory T cells (TRM), resides in NLTwithout recirculating (Masopust and Schenkel, 2013; Mueller et al., 2013).”
Chemokines and chemokine receptors: positioning cells for host defense and immunity. (2014, background): “As recently reviewed, these cells have been definitively identified in the skin, vaginal mucosa, central nervous system, salivary gland, lung, and intestine and are characterized by the increased expression of CD103 and CD69 and a lack of CD62L and CCR7 (208).”
Tissue-Resident Memory T Cells (2014, background): “Mechanisms of Trm Maintenance In order for Trm cells to be maintained within tissues, they must adapt to local survival cues, resist shedding into the lumen at mucosal epithelial surfaces, and ignore egress signals (Masopust and Schenkel, 2013; Mueller et al., 2013).”