T cell memory.

By J. T. Tan, C. Surh. Current Topics in Microbiology and Immunology, 2006

918 citations recorded by the source corpus.

Subfields: Immunology

View Paper: https://www.semanticscholar.org/paper/58840f42b08ad177b2a45af44126ef6ce6778552

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Immunology

1. J. Schenkel
2. D. Masopust
3. S. Kaech
4. W. Cui
5. D. Farber
6. Brahma V. Kumar
7. L. Gapin
8. Y. Bryceson

Citations in the corpus

• Naive CD4(+) T cell frequency varies for different epitopes and predicts repertoire diversity and response magnitude. (2007, background): “Anti-CD44 antibody was also included in the staining cocktail to identify CD44high antigen-experienced cells (Dutton et al., 1998).”
• Inflammation directs memory precursor and short-lived effector CD8(+) T cell fates via the graded expression of T-bet transcription factor. (2007, background): “Historically, identification of MPECs and SLECs within the effector CD8 T cell population has proven difficult because most of the T cell attributes first studied (e.g. CD44hi and CD11ahi) were acquired uniformly by effector CD8 T cells (Dutton et al., 1998).”
• Human tissue-resident memory T cells are defined by core transcriptional and functional signatures in lymphoid and mucosal sites (2017, background): “While TRMs have been detected in mouse lymph nodes (Schenkel et al., 2014b; Ugur et al., 2014), the majority of mouse lymphoid memory CD4+ and CD8+ T cells in mice are circulating, particularly those in the spleen.”
• Tissue-Resident Memory T Cells (2014, background): “…productively primed within SLOs, they give rise to effector cells that migrate throughout the host and leave behind a memory population that persists long after pathogen clearance (Dutton et al., 1998; Harty and Badovinac, 2008; Lefrançois, 2006; Sallusto et al., 2010; Williams and Bevan, 2007).”
• CD49a Expression Defines Tissue-Resident CD8+ T Cells Poised for Cytotoxic Function in Human Skin (2017, positive): “Following in situ activation, Trm cells provide strong defense against recurrent infections (Ariotti et al., 2014; Schenkel et al., 2014).”