Laura K Mackay, Azad Rahimpour, Joel Z Ma, Nicholas Collins, Angus T Stock, Ming-Li Hafon, Javier Vega-Ramos, Pilar Lauzurica, Scott N Mueller, Tijana Stefanovic, David C Tscharke, William R Heath, Michael Inouye, Francis R Carbone, Thomas Gebhardt. Nat Immunol 2013
Times Cited: 715
Times Cited: 715
Times Cited
Times Co-cited
Similarity
Hobit and Blimp1 instruct a universal transcriptional program of tissue residency in lymphocytes.
Laura K Mackay, Martina Minnich, Natasja A M Kragten, Yang Liao, Benjamin Nota, Cyril Seillet, Ali Zaid, Kevin Man, Simon Preston, David Freestone,[...]. Science 2016
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Human Tissue-Resident Memory T Cells Are Defined by Core Transcriptional and Functional Signatures in Lymphoid and Mucosal Sites.
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Runx3 programs CD8+ T cell residency in non-lymphoid tissues and tumours.
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T-box Transcription Factors Combine with the Cytokines TGF-β and IL-15 to Control Tissue-Resident Memory T Cell Fate.
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Transcriptional downregulation of S1pr1 is required for the establishment of resident memory CD8+ T cells.
Cara N Skon, June-Yong Lee, Kristin G Anderson, David Masopust, Kristin A Hogquist, Stephen C Jameson. Nat Immunol 2013
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Antigen-independent differentiation and maintenance of effector-like resident memory T cells in tissues.
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Sensing and alarm function of resident memory CD8⁺ T cells.
Jason M Schenkel, Kathryn A Fraser, Vaiva Vezys, David Masopust. Nat Immunol 2013
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Programs for the persistence, vigilance and control of human CD8+ lung-resident memory T cells.
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CD49a Expression Defines Tissue-Resident CD8+ T Cells Poised for Cytotoxic Function in Human Skin.
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Transforming growth factor-β signaling controls the formation and maintenance of gut-resident memory T cells by regulating migration and retention.
Nu Zhang, Michael J Bevan. Immunity 2013
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Local proliferation maintains a stable pool of tissue-resident memory T cells after antiviral recall responses.
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Survival of tissue-resident memory T cells requires exogenous lipid uptake and metabolism.
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Tissue-resident memory T cells: local specialists in immune defence.
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Developmental plasticity allows outside-in immune responses by resident memory T cells.
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Quantifying Memory CD8 T Cells Reveals Regionalization of Immunosurveillance.
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Memory T cells in nonlymphoid tissue that provide enhanced local immunity during infection with herpes simplex virus.
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Human skin is protected by four functionally and phenotypically discrete populations of resident and recirculating memory T cells.
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Long-lived epithelial immunity by tissue-resident memory T (TRM) cells in the absence of persisting local antigen presentation.
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T cell memory. Resident memory CD8 T cells trigger protective innate and adaptive immune responses.
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Skin infection generates non-migratory memory CD8+ T(RM) cells providing global skin immunity.
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T cell memory. Skin-resident memory CD8⁺ T cells trigger a state of tissue-wide pathogen alert.
Silvia Ariotti, Marc A Hogenbirk, Feline E Dijkgraaf, Lindy L Visser, Mirjam E Hoekstra, Ji-Ying Song, Heinz Jacobs, John B Haanen, Ton N Schumacher. Science 2014
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Liver-Resident Memory CD8+ T Cells Form a Front-Line Defense against Malaria Liver-Stage Infection.
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Cutting edge: CD69 interference with sphingosine-1-phosphate receptor function regulates peripheral T cell retention.
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Two subsets of memory T lymphocytes with distinct homing potentials and effector functions.
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Dynamic T cell migration program provides resident memory within intestinal epithelium.
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Location, location, location: Tissue resident memory T cells in mice and humans.
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T Cells in Nonlymphoid Tissues Give Rise to Lymph-Node-Resident Memory T Cells.
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IL-15-Independent Maintenance of Tissue-Resident and Boosted Effector Memory CD8 T Cells.
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Tissue-Resident T Cells and Other Resident Leukocytes.
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Oral infection drives a distinct population of intestinal resident memory CD8(+) T cells with enhanced protective function.
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Heterogenous Populations of Tissue-Resident CD8+ T Cells Are Generated in Response to Infection and Malignancy.
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CD4+ T cell help guides formation of CD103+ lung-resident memory CD8+ T cells during influenza viral infection.
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KLRG1+ Effector CD8+ T Cells Lose KLRG1, Differentiate into All Memory T Cell Lineages, and Convey Enhanced Protective Immunity.
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Intravital mucosal imaging of CD8+ resident memory T cells shows tissue-autonomous recall responses that amplify secondary memory.
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Migratory DCs activate TGF-β to precondition naïve CD8+ T cells for tissue-resident memory fate.
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Early precursors and molecular determinants of tissue-resident memory CD8+ T lymphocytes revealed by single-cell RNA sequencing.
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Brain-resident memory T cells represent an autonomous cytotoxic barrier to viral infection.
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Inflammation directs memory precursor and short-lived effector CD8(+) T cell fates via the graded expression of T-bet transcription factor.
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Hair follicle-derived IL-7 and IL-15 mediate skin-resident memory T cell homeostasis and lymphoma.
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CD69 acts downstream of interferon-alpha/beta to inhibit S1P1 and lymphocyte egress from lymphoid organs.
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Tissue-resident memory CD8+ T cells shape local and systemic secondary T cell responses.
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Proinflammatory microenvironments within the intestine regulate the differentiation of tissue-resident CD8⁺ T cells responding to infection.
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Persistence of skin-resident memory T cells within an epidermal niche.
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Different patterns of peripheral migration by memory CD4+ and CD8+ T cells.
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The Chemokine Receptor CX3CR1 Defines Three Antigen-Experienced CD8 T Cell Subsets with Distinct Roles in Immune Surveillance and Homeostasis.
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CD4+ resident memory T cells dominate immunosurveillance and orchestrate local recall responses.
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Hobit- and Blimp-1-driven CD4+ tissue-resident memory T cells control chronic intestinal inflammation.
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A vaccine strategy that protects against genital herpes by establishing local memory T cells.
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The molecular signature of tissue resident memory CD8 T cells isolated from the brain.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.