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Progressive change in expression of killer-like receptorsr and GPR56 expression defines the cytokine production potential of human CD4 + T memory cells

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/1521-4141(200101)31:1<233::aid-immu233>3.0.co;2-4openalex-snapshot
Identification of NKp80, a novel triggering molecule expressed by human NK cells
inferredcites →https://doi.org/10.1002/art.34647openalex-snapshot
Th1 and Th17 lymphocytes expressing CD161 are implicated in giant cell arteritis and polymyalgia rheumatica pathogenesis
inferredcites →https://doi.org/10.1002/eji.200424958openalex-snapshot
Diverse populations of T cells with NK cell receptors accumulate in the human intestine in health and in colorectal cancer
inferredcites →https://doi.org/10.1002/eji.200737611openalex-snapshot
Characterization of a subset of antigen‐specific human central memory CD4+ T lymphocytes producing effector cytokines
inferredcites →https://doi.org/10.1002/eji.200737852openalex-snapshot
The strength of T cell stimulation determines IL‐7 responsiveness, secondary expansion, and lineage commitment of primed human CD4+IL‐7Rhi T cells
inferredcites →https://doi.org/10.1002/eji.200738044openalex-snapshot
Fine‐tuning CD4+ central memory T cell heterogeneity by strength of stimulation
inferredcites →https://doi.org/10.1002/eji.200940257openalex-snapshot
CD161 is a marker of all human IL‐17‐producing T‐cell subsets and is induced by RORC
inferredcites →https://doi.org/10.1002/eji.201747018openalex-snapshot
CMV drives the expansion of highly functional memory T cells expressing NK‐cell receptors in renal transplant recipients
inferredcites →https://doi.org/10.1007/82_2014_401openalex-snapshot
Memory CD4 T Cells in Influenza
inferredcites →https://doi.org/10.1007/978-1-4615-0757-4_14openalex-snapshot
Tcr-Independent Proliferation and Differentiation of Human Cd4+ T Cell Subsets Induced by Cytokines
inferredcites →https://doi.org/10.1007/978-3-642-57276-0_21openalex-snapshot
Functional Subsets of Memory T Cells Identified by CCR7 Expression
inferredcites →https://doi.org/10.1016/j.bbmt.2013.10.022openalex-snapshot
Prevention of Graft-versus-Host Disease by Adoptive T Regulatory Therapy Is Associated with Active Repression of Peripheral Blood Toll-Like Receptor 5 mRNA Expression
inferredcites →https://doi.org/10.1016/j.cell.2014.04.005openalex-snapshot
Single-Cell Trajectory Detection Uncovers Progression and Regulatory Coordination in Human B Cell Development
inferredcites →https://doi.org/10.1016/j.cell.2014.10.026openalex-snapshot
Spatial Map of Human T Cell Compartmentalization and Maintenance over Decades of Life
inferredcites →https://doi.org/10.1016/j.celrep.2014.09.045openalex-snapshot
CD161 Defines a Transcriptional and Functional Phenotype across Distinct Human T Cell Lineages
inferredcites →https://doi.org/10.1016/j.celrep.2016.04.053openalex-snapshot
The Adhesion G Protein-Coupled Receptor GPR56/ADGRG1 Is an Inhibitory Receptor on Human NK Cells
inferredcites →https://doi.org/10.1016/j.coi.2012.04.001openalex-snapshot
Properties of end-stage human T cells defined by CD45RA re-expression
inferredcites →https://doi.org/10.1016/j.immuni.2013.05.009openalex-snapshot
Effector-like CD8+ T Cells in the Memory Population Mediate Potent Protective Immunity
inferredcites →https://doi.org/10.1016/j.immuni.2014.01.005openalex-snapshot
Molecular and Transcriptional Basis of CD4+ T Cell Dysfunction during Chronic Infection
inferredcites →https://doi.org/10.1016/j.it.2015.05.003openalex-snapshot
Emerging concepts in tissue-resident T cells: lessons from humans
inferredcites →https://doi.org/10.1016/j.it.2015.07.002openalex-snapshot
Tissue instruction for migration and retention of TRM cells
inferredcites →https://doi.org/10.1016/j.it.2016.09.002openalex-snapshot
Senescence of T Lymphocytes: Implications for Enhancing Human Immunity
inferredcites →https://doi.org/10.1038/nbt.1991openalex-snapshot
Extracting a cellular hierarchy from high-dimensional cytometry data with SPADE
inferredcites →https://doi.org/10.1038/nbt.2594openalex-snapshot
viSNE enables visualization of high dimensional single-cell data and reveals phenotypic heterogeneity of leukemia
inferredcites →https://doi.org/10.1038/ncomms9306openalex-snapshot
Functional classification of memory CD8+ T cells by CX3CR1 expression
inferredcites →https://doi.org/10.1038/ni.1679openalex-snapshot
Coregulation of CD8+ T cell exhaustion by multiple inhibitory receptors during chronic viral infection
inferredcites →https://doi.org/10.1038/ni.2035openalex-snapshot
T cell exhaustion
inferredcites →https://doi.org/10.1038/ni.2613openalex-snapshot
Deconstructing development
inferredcites →https://doi.org/10.1038/ni.3031openalex-snapshot
Molecular regulation of effector and memory T cell differentiation
inferredcites →https://doi.org/10.1038/nm.4008openalex-snapshot
Early-life compartmentalization of human T cell differentiation and regulatory function in mucosal and lymphoid tissues
inferredcites →https://doi.org/10.1038/nri2274openalex-snapshot
T-cell quality in memory and protection: implications for vaccine design
inferredcites →https://doi.org/10.1038/nri3862openalex-snapshot
Molecular and cellular insights into T cell exhaustion
inferredcites →https://doi.org/10.1073/pnas.1013084108openalex-snapshot
Single-cell gene-expression profiling reveals qualitatively distinct CD8 T cells elicited by different gene-based vaccines
inferredcites →https://doi.org/10.1111/imr.12426openalex-snapshot
CD 4+ T‐cell help amplifies innate signals for primary CD 8+ T‐cell immunity
inferredcites →https://doi.org/10.1111/j.1365-2567.2010.03386.xopenalex-snapshot
Cytomegalovirus infection induces the accumulation of short-lived, multifunctional CD4+ CD45RA+ CD27− T cells: the potential involvement of interleukin-7 in this process
inferredcites →https://doi.org/10.1136/annrheumdis-2013-203881openalex-snapshot
Senescence marker killer cell lectin-like receptor G1 (KLRG1) contributes to TNF-α production by interaction with its soluble E-cadherin ligand in chronically inflamed joints
inferredcites →https://doi.org/10.1146/annurev.immunol.22.012703.104702openalex-snapshot
Central Memory and Effector Memory T Cell Subsets: Function, Generation, and Maintenance
inferredcites →https://doi.org/10.1155/2015/327470openalex-snapshot
T Helper Lymphocyte Subsets and Plasticity in Autoimmunity and Cancer: An Overview
inferredcites →https://doi.org/10.1155/2017/7083153openalex-snapshot
CD4+ T Helper Cell Plasticity in Infection, Inflammation, and Autoimmunity
inferredcites →https://doi.org/10.1182/blood-2002-02-0657openalex-snapshot
Lack of proliferative capacity of human effector and memory T cells expressing killer cell lectinlike receptor G1 (KLRG1)
inferredcites →https://doi.org/10.1182/blood-2002-11-3577openalex-snapshot
Proliferation and differentiation potential of human CD8+ memory T-cell subsets in response to antigen or homeostatic cytokines
inferredcites →https://doi.org/10.1182/blood-2008-03-145615openalex-snapshot
NKp80 defines and stimulates a reactive subset of CD8 T cells
inferredcites →https://doi.org/10.1189/jlb.0211092openalex-snapshot
Specific expression of GPR56 by human cytotoxic lymphocytes
inferredcites →https://doi.org/10.1371/journal.pone.0123591openalex-snapshot
CD161 Expression Defines a Th1/Th17 Polyfunctional Subset of Resident Memory T Lymphocytes in Bronchoalveolar Cells
inferredcites →https://doi.org/10.1371/journal.ppat.1005219openalex-snapshot
Phenotypic and Functional Alterations in Circulating Memory CD8 T Cells with Time after Primary Infection
inferredcites →https://doi.org/10.4049/jimmunol.1100978openalex-snapshot
Reversible Senescence in Human CD4+CD45RA+CD27− Memory T Cells
inferredcites →https://doi.org/10.4049/jimmunol.1402669openalex-snapshot
Tapping CD4 T Cells for Cancer Immunotherapy: The Choice of Personalized Genomics
inferredcites →https://doi.org/10.4049/jimmunol.176.1.211openalex-snapshot
Expression of CD161 (NKR-P1A) Defines Subsets of Human CD4 and CD8 T Cells with Different Functional Activities
inferredcites →https://doi.org/10.7554/elife.08133openalex-snapshot
TGFβ-dependent expression of PD-1 and PD-L1 controls CD8+ T cell anergy in transplant tolerance

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.3389/fimmu.2019.00408openalex-snapshot
Adipose Tissue in Persons With HIV Is Enriched for CD4+ T Effector Memory and T Effector Memory RA+ Cells, Which Show Higher CD69 Expression and CD57, CX3CR1, GPR56 Co-expression With Increasing Glucose Intolerance
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