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Area under Immunosurveillance: Dedicated Roles of Memory CD8 T-Cell Subsets

https://doi.org/10.1101/cshperspect.a037796

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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/cyto.a.20643openalex-snapshot

Phenotype and function of human T lymphocyte subsets: Consensus and issues

inferredcites →https://doi.org/10.1002/eji.200635874openalex-snapshot

Unidirectional development of CD8+ central memory T cells into protective Listeria‐specific effector memory T cells

inferredcites →https://doi.org/10.1002/eji.201847771openalex-snapshot

Blimp‐1 induces and Hobit maintains the cytotoxic mediator granzyme B in CD8 T cells

inferredcites →https://doi.org/10.1016/j.cell.2012.08.015openalex-snapshot

Chemokine Guidance of Central Memory T Cells Is Critical for Antiviral Recall Responses in Lymph Nodes

inferredcites →https://doi.org/10.1016/j.cell.2015.03.031openalex-snapshot

Quantifying Memory CD8 T Cells Reveals Regionalization of Immunosurveillance

inferredcites →https://doi.org/10.1016/j.cell.2017.08.024openalex-snapshot

Organism-Level Analysis of Vaccination Reveals Networks of Protection across Tissues

inferredcites →https://doi.org/10.1016/j.celrep.2013.07.008openalex-snapshot

Low-Affinity T Cells Are Programmed to Maintain Normal Primary Responses but Are Impaired in Their Recall to Low-Affinity Ligands

inferredcites →https://doi.org/10.1016/j.celrep.2015.09.082openalex-snapshot

The Salivary Gland Acts as a Sink for Tissue-Resident Memory CD8+ T Cells, Facilitating Protection from Local Cytomegalovirus Infection

inferredcites →https://doi.org/10.1016/j.celrep.2017.03.031openalex-snapshot

Local Inflammatory Cues Regulate Differentiation and Persistence of CD8+ Tissue-Resident Memory T Cells

inferredcites →https://doi.org/10.1016/j.celrep.2017.04.014openalex-snapshot

Label-free Analysis of CD8+ T Cell Subset Proteomes Supports a Progressive Differentiation Model of Human-Virus-Specific T Cells

inferredcites →https://doi.org/10.1016/j.celrep.2017.08.078openalex-snapshot

Human Tissue-Resident Memory T Cells Are Defined by Core Transcriptional and Functional Signatures in Lymphoid and Mucosal Sites

inferredcites →https://doi.org/10.1016/j.celrep.2018.01.072openalex-snapshot

Suppression of Tcf1 by Inflammatory Cytokines Facilitates Effector CD8 T Cell Differentiation

inferredcites →https://doi.org/10.1016/j.coi.2013.09.003openalex-snapshot

Lineage relationship of effector and memory T cells

inferredcites →https://doi.org/10.1016/j.coviro.2016.11.011openalex-snapshot

Tissue resident memory T cells and viral immunity

inferredcites →https://doi.org/10.1016/j.immuni.2006.08.022openalex-snapshot

Persistence and Responsiveness of Immunologic Memory in the Absence of Secondary Lymphoid Organs

inferredcites →https://doi.org/10.1016/j.immuni.2007.04.013openalex-snapshot

Initial T Cell Receptor Transgenic Cell Precursor Frequency Dictates Critical Aspects of the CD8+ T Cell Response to Infection

inferredcites →https://doi.org/10.1016/j.immuni.2007.07.010openalex-snapshot

Inflammation Directs Memory Precursor and Short-Lived Effector CD8+ T Cell Fates via the Graded Expression of T-bet Transcription Factor

inferredcites →https://doi.org/10.1016/j.immuni.2007.10.012openalex-snapshot

A Single Naive CD8+ T Cell Precursor Can Develop into Diverse Effector and Memory Subsets

inferredcites →https://doi.org/10.1016/j.immuni.2008.04.010openalex-snapshot

Endogenous Naive CD8+ T Cell Precursor Frequency Regulates Primary and Memory Responses to Infection

inferredcites →https://doi.org/10.1016/j.immuni.2008.11.002openalex-snapshot

Homeostasis of Naive and Memory T Cells

inferredcites →https://doi.org/10.1016/j.immuni.2009.05.014openalex-snapshot

Transcriptional Repressor Blimp-1 Promotes CD8+ T Cell Terminal Differentiation and Represses the Acquisition of Central Memory T Cell Properties

inferredcites →https://doi.org/10.1016/j.immuni.2009.06.021openalex-snapshot

Blimp-1 Transcription Factor Is Required for the Differentiation of Effector CD8+ T Cells and Memory Responses

inferredcites →https://doi.org/10.1016/j.immuni.2009.09.017openalex-snapshot

Macrophage- and Dendritic-Cell-Derived Interleukin-15 Receptor Alpha Supports Homeostasis of Distinct CD8+ T Cell Subsets

inferredcites →https://doi.org/10.1016/j.immuni.2009.11.010openalex-snapshot

Prolonged Interleukin-2Rα Expression on Virus-Specific CD8+ T Cells Favors Terminal-Effector Differentiation In Vivo

inferredcites →https://doi.org/10.1016/j.immuni.2009.11.012openalex-snapshot

Interleukin-2 and Inflammation Induce Distinct Transcriptional Programs that Promote the Differentiation of Effector Cytolytic T Cells

inferredcites →https://doi.org/10.1016/j.immuni.2010.06.014openalex-snapshot

Repetitive Antigen Stimulation Induces Stepwise Transcriptome Diversification but Preserves a Core Signature of Memory CD8+ T Cell Differentiation

inferredcites →https://doi.org/10.1016/j.immuni.2010.08.002openalex-snapshot

Differentiation and Persistence of Memory CD8+ T Cells Depend on T Cell Factor 1

inferredcites →https://doi.org/10.1016/j.immuni.2011.03.020openalex-snapshot

Protective Capacity of Memory CD8+ T Cells Is Dictated by Antigen Exposure History and Nature of the Infection

inferredcites →https://doi.org/10.1016/j.immuni.2012.11.012openalex-snapshot

Peripheral Prepositioning and Local CXCL9 Chemokine-Mediated Guidance Orchestrate Rapid Memory CD8+ T Cell Responses in the Lymph Node

inferredcites →https://doi.org/10.1016/j.immuni.2013.08.019openalex-snapshot

Transforming Growth Factor-β Signaling Controls the Formation and Maintenance of Gut-Resident Memory T Cells by Regulating Migration and Retention

inferredcites →https://doi.org/10.1016/j.immuni.2013.08.034openalex-snapshot

Antigen Availability Determines CD8+ T Cell-Dendritic Cell Interaction Kinetics and Memory Fate Decisions

inferredcites →https://doi.org/10.1016/j.immuni.2014.03.007openalex-snapshot

Oral Infection Drives a Distinct Population of Intestinal Resident Memory CD8+ T Cells with Enhanced Protective Function

inferredcites →https://doi.org/10.1016/j.immuni.2014.05.018openalex-snapshot

Serial Transfer of Single-Cell-Derived Immunocompetence Reveals Stemness of CD8+ Central Memory T Cells

inferredcites →https://doi.org/10.1016/j.immuni.2014.09.007openalex-snapshot

CD4+ T Cell Help Guides Formation of CD103+ Lung-Resident Memory CD8+ T Cells during Influenza Viral Infection

inferredcites →https://doi.org/10.1016/j.immuni.2015.11.008openalex-snapshot

T-box Transcription Factors Combine with the Cytokines TGF-β and IL-15 to Control Tissue-Resident Memory T Cell Fate

inferredcites →https://doi.org/10.1016/j.immuni.2016.07.007openalex-snapshot

A High-Dimensional Atlas of Human T Cell Diversity Reveals Tissue-Specific Trafficking and Cytokine Signatures

inferredcites →https://doi.org/10.1016/j.immuni.2016.08.011openalex-snapshot

Liver-Resident Memory CD8+ T Cells Form a Front-Line Defense against Malaria Liver-Stage Infection

inferredcites →https://doi.org/10.1016/j.immuni.2016.08.019openalex-snapshot

Optimal Generation of Tissue-Resident but Not Circulating Memory T Cells during Viral Infection Requires Crosspriming by DNGR-1 + Dendritic Cells

inferredcites →https://doi.org/10.1016/j.immuni.2016.10.018openalex-snapshot

The Chemokine Receptor CX3CR1 Defines Three Antigen-Experienced CD8 T Cell Subsets with Distinct Roles in Immune Surveillance and Homeostasis

inferredcites →https://doi.org/10.1016/j.immuni.2017.01.009openalex-snapshot

CD49a Expression Defines Tissue-Resident CD8 + T Cells Poised for Cytotoxic Function in Human Skin

inferredcites →https://doi.org/10.1016/j.immuni.2018.01.015openalex-snapshot

T Cells in Nonlymphoid Tissues Give Rise to Lymph-Node-Resident Memory T Cells

inferredcites →https://doi.org/10.1016/j.immuni.2018.03.015openalex-snapshot

KLRG1+ Effector CD8+ T Cells Lose KLRG1, Differentiate into All Memory T Cell Lineages, and Convey Enhanced Protective Immunity

inferredcites →https://doi.org/10.1016/j.immuni.2019.03.002openalex-snapshot

Keratinocyte-Mediated Activation of the Cytokine TGF-β Maintains Skin Recirculating Memory CD8+ T Cells

inferredcites →https://doi.org/10.1016/s1074-7613(00)80469-0openalex-snapshot

Massive Expansion of Antigen-Specific CD8+ T Cells during an Acute Virus Infection

inferredcites →https://doi.org/10.1016/s1074-7613(00)80564-6openalex-snapshot

Potent and Selective Stimulation of Memory-Phenotype CD8+ T Cells In Vivo by IL-15

inferredcites →https://doi.org/10.1038/21208openalex-snapshot

Modelling T-cell memory by genetic marking of memory T cells in vivo

inferredcites →https://doi.org/10.1038/369648a0openalex-snapshot

Cytotoxic T-cell memory without antigen

inferredcites →https://doi.org/10.1038/369652a0openalex-snapshot

Virus-specific CD8+ T-cell memory determined by clonal burst size

inferredcites →https://doi.org/10.1038/44385openalex-snapshot

Two subsets of memory T lymphocytes with distinct homing potentials and effector functions

inferredcites →https://doi.org/10.1038/80868openalex-snapshot

Interleukin-7 mediates the homeostasis of naïve and memory CD8 T cells in vivo

inferredcites →https://doi.org/10.1038/cmi.2015.32openalex-snapshot

Lineage relationship of CD8+ T cell subsets is revealed by progressive changes in the epigenetic landscape

inferredcites →https://doi.org/10.1038/nature02284openalex-snapshot

Lymphocyte egress from thymus and peripheral lymphoid organs is dependent on S1P receptor 1

inferredcites →https://doi.org/10.1038/nature04606openalex-snapshot

CD69 acts downstream of interferon-α/β to inhibit S1P1 and lymphocyte egress from lymphoid organs

inferredcites →https://doi.org/10.1038/nature06672openalex-snapshot

Memory CD4 T cells emerge from effector T-cell progenitors

inferredcites →https://doi.org/10.1038/nature07486openalex-snapshot

Memory CD8 T-cell compartment grows in size with immunological experience

inferredcites →https://doi.org/10.1038/nature07657openalex-snapshot

Complete but curtailed T-cell response to very low-affinity antigen

inferredcites →https://doi.org/10.1038/nature08511openalex-snapshot

CD8+ T lymphocyte mobilization to virus-infected tissue requires CD4+ T-cell help

inferredcites →https://doi.org/10.1038/nature10851openalex-snapshot

Skin infection generates non-migratory memory CD8+ TRM cells providing global skin immunity

inferredcites →https://doi.org/10.1038/nature24633openalex-snapshot

Origin and differentiation of human memory CD8 T cells after vaccination

inferredcites →https://doi.org/10.1038/nature24993openalex-snapshot

Runx3 programs CD8+ T cell residency in non-lymphoid tissues and tumours

inferredcites →https://doi.org/10.1038/nature25144openalex-snapshot

Effector CD8 T cells dedifferentiate into long-lived memory cells

inferredcites →https://doi.org/10.1038/ncomms16073openalex-snapshot

Enhanced anti-tumour immunity requires the interplay between resident and circulating memory CD8+ T cells

inferredcites →https://doi.org/10.1038/ni.1718openalex-snapshot

Memory T cells in nonlymphoid tissue that provide enhanced local immunity during infection with herpes simplex virus

inferredcites →https://doi.org/10.1038/ni.2079openalex-snapshot

Autocrine IL-2 is required for secondary population expansion of CD8+ memory T cells

inferredcites →https://doi.org/10.1038/ni.2568openalex-snapshot

Sensing and alarm function of resident memory CD8+ T cells

inferredcites →https://doi.org/10.1038/ni.2744openalex-snapshot

The developmental pathway for CD103+CD8+ tissue-resident memory T cells of skin

inferredcites →https://doi.org/10.1038/ni.2745openalex-snapshot

Transcriptional downregulation of S1pr1 is required for the establishment of resident memory CD8+ T cells

inferredcites →https://doi.org/10.1038/ni.2842openalex-snapshot

Early specification of CD8+ T lymphocyte fates during adaptive immunity revealed by single-cell gene-expression analyses

inferredcites →https://doi.org/10.1038/ni.3027openalex-snapshot

A central role for Notch in effector CD8+ T cell differentiation

inferredcites →https://doi.org/10.1038/ni.3108openalex-snapshot

Proinflammatory microenvironments within the intestine regulate the differentiation of tissue-resident CD8+ T cells responding to infection

inferredcites →https://doi.org/10.1038/ni.3396openalex-snapshot

Stromal cells control the epithelial residence of DCs and memory T cells by regulated activation of TGF-β

inferredcites →https://doi.org/10.1038/ni.3438openalex-snapshot

Asymmetric inheritance of mTORC1 kinase activity during division dictates CD8+ T cell differentiation

inferredcites →https://doi.org/10.1038/ni.3589openalex-snapshot

Programs for the persistence, vigilance and control of human CD8+ lung-resident memory T cells

inferredcites →https://doi.org/10.1038/ni.3688openalex-snapshot

Early transcriptional and epigenetic regulation of CD8+ T cell differentiation revealed by single-cell RNA sequencing

inferredcites →https://doi.org/10.1038/ni1009openalex-snapshot

Selective expression of the interleukin 7 receptor identifies effector CD8 T cells that give rise to long-lived memory cells

inferredcites →https://doi.org/10.1038/ni1098openalex-snapshot

CD8+ T cell contraction is controlled by early inflammation

inferredcites →https://doi.org/10.1038/ni1227openalex-snapshot

Initial T cell frequency dictates memory CD8+ T cell lineage commitment

inferredcites →https://doi.org/10.1038/ni1513openalex-snapshot

Fibroblastic reticular cells in lymph nodes regulate the homeostasis of naive T cells

inferredcites →https://doi.org/10.1038/ni889openalex-snapshot

Lineage relationship and protective immunity of memory CD8 T cell subsets

inferredcites →https://doi.org/10.1038/nm.1982openalex-snapshot

Wnt signaling arrests effector T cell differentiation and generates CD8+ memory stem cells

inferredcites →https://doi.org/10.1038/nm.2446openalex-snapshot

A human memory T cell subset with stem cell–like properties

inferredcites →https://doi.org/10.1038/nm.3962openalex-snapshot

Hair follicle–derived IL-7 and IL-15 mediate skin-resident memory T cell homeostasis and lymphoma

inferredcites →https://doi.org/10.1038/nm.4241openalex-snapshot

T memory stem cells in health and disease

inferredcites →https://doi.org/10.1038/nm917openalex-snapshot

Duration of antiviral immunity after smallpox vaccination

inferredcites →https://doi.org/10.1038/nri.2015.3openalex-snapshot

Tissue-resident memory T cells: local specialists in immune defence

inferredcites →https://doi.org/10.1038/nri1351openalex-snapshot

Selectins in T-cell recruitment to non-lymphoid tissues and sites of inflammation

inferredcites →https://doi.org/10.1038/nri2297openalex-snapshot

CCR7 and its ligands: balancing immunity and tolerance

inferredcites →https://doi.org/10.1038/s41467-018-07053-9openalex-snapshot

Tissue-resident memory T cells populate the human brain

inferredcites →https://doi.org/10.1038/s41590-017-0027-5openalex-snapshot

Local proliferation maintains a stable pool of tissue-resident memory T cells after antiviral recall responses

inferredcites →https://doi.org/10.1038/s41590-017-0029-3openalex-snapshot

Intravital mucosal imaging of CD8+ resident memory T cells shows tissue-autonomous recall responses that amplify secondary memory

inferredcites →https://doi.org/10.1073/pnas.0603289103openalex-snapshot

Early establishment of diverse T cell receptor profiles for influenza-specific CD8 + CD62L hi memory T cells

inferredcites →https://doi.org/10.1073/pnas.1107200108openalex-snapshot

E-cadherin promotes accumulation of a unique memory CD8 T-cell population in murine salivary glands

inferredcites →https://doi.org/10.1073/pnas.1202288109openalex-snapshot

Long-lived epithelial immunity by tissue-resident memory T (T RM ) cells in the absence of persisting local antigen presentation

inferredcites →https://doi.org/10.1073/pnas.93.24.14002openalex-snapshot

A functional interleukin 12 receptor complex is composed of two β-type cytokine receptor subunits

inferredcites →https://doi.org/10.1073/pnas.95.1.258openalex-snapshot

A chemokine expressed in lymphoid high endothelial venules promotes the adhesion and chemotaxis of naive T lymphocytes

inferredcites →https://doi.org/10.1073/pnas.96.6.2976openalex-snapshot

Functional differences between memory and naive CD8 T cells

inferredcites →https://doi.org/10.1084/jem.193.9.1105openalex-snapshot

The Ccr7 Ligand ELC (Ccl19) Is Transcytosed in High Endothelial Venules and Mediates T Cell Recruitment

inferredcites →https://doi.org/10.1084/jem.20020033openalex-snapshot

Cytokine Requirements for Acute and Basal Homeostatic Proliferation of Naive and Memory CD8+ T Cells

inferredcites →https://doi.org/10.1084/jem.20020066openalex-snapshot

Interleukin (IL)-15 and IL-7 Jointly Regulate Homeostatic Proliferation of Memory Phenotype CD8+ Cells but Are Not Required for Memory Phenotype CD4+ Cells

inferredcites →https://doi.org/10.1084/jem.20020369openalex-snapshot

Interleukin 15 Is Required for Proliferative Renewal of Virus-specific Memory CD8 T Cells

inferredcites →https://doi.org/10.1084/jem.20031799openalex-snapshot

Immediate Cytotoxicity But Not Degranulation Distinguishes Effector and Memory Subsets of CD8+ T Cells

inferredcites →https://doi.org/10.1084/jem.20041509openalex-snapshot

Cyclical modulation of sphingosine-1-phosphate receptor 1 surface expression during lymphocyte recirculation and relationship to lymphoid organ transit

inferredcites →https://doi.org/10.1084/jem.20052237openalex-snapshot

Secondary memory CD8+ T cells are more protective but slower to acquire a central–memory phenotype

inferredcites →https://doi.org/10.1084/jem.20081242openalex-snapshot

Runx3 and T-box proteins cooperate to establish the transcriptional program of effector CTLs

inferredcites →https://doi.org/10.1084/jem.20090858openalex-snapshot

Dynamic T cell migration program provides resident memory within intestinal epithelium

inferredcites →https://doi.org/10.1084/jem.20151855openalex-snapshot

Local antigen in nonlymphoid tissue promotes resident memory CD8+ T cell formation during viral infection

inferredcites →https://doi.org/10.1084/jem.20151916openalex-snapshot

Brain-resident memory T cells represent an autonomous cytotoxic barrier to viral infection

inferredcites →https://doi.org/10.1084/jem.20161760openalex-snapshot

Human memory CD8 T cell effector potential is epigenetically preserved during in vivo homeostasis

inferredcites →https://doi.org/10.1084/jem.20181308openalex-snapshot

CXCR6 regulates localization of tissue-resident memory CD8 T cells to the airways

inferredcites →https://doi.org/10.1084/jem.20190557openalex-snapshot

Interstitial-resident memory CD8+ T cells sustain frontline epithelial memory in the lung

inferredcites →https://doi.org/10.1098/rspb.1964.0001openalex-snapshot

The route of re-circulation of lymphocytes in the rat

inferredcites →https://doi.org/10.1126/science.1139393openalex-snapshot

Asymmetric T Lymphocyte Division in the Initiation of Adaptive Immune Responses

inferredcites →https://doi.org/10.1126/science.1166831openalex-snapshot

Secondary Replicative Function of CD8 + T Cells That Had Developed an Effector Phenotype

inferredcites →https://doi.org/10.1126/science.1235454openalex-snapshot

Disparate Individual Fates Compose Robust CD8 + T Cell Immunity

inferredcites →https://doi.org/10.1126/science.1235487openalex-snapshot

Heterogeneous Differentiation Patterns of Individual CD8 + T Cells

inferredcites →https://doi.org/10.1126/science.1254536openalex-snapshot

Resident memory CD8 T cells trigger protective innate and adaptive immune responses

inferredcites →https://doi.org/10.1126/science.1254803openalex-snapshot

Skin-resident memory CD8 + T cells trigger a state of tissue-wide pathogen alert

inferredcites →https://doi.org/10.1126/science.1257530openalex-snapshot

A local macrophage chemokine network sustains protective tissue-resident memory CD4 T cells

inferredcites →https://doi.org/10.1126/science.279.5356.1552openalex-snapshot

Sphingosine-1-Phosphate as a Ligand for the G Protein-Coupled Receptor EDG-1

inferredcites →https://doi.org/10.1126/science.286.5443.1377openalex-snapshot

Persistence of Memory CD8 T Cells in MHC Class I-Deficient Mice

inferredcites →https://doi.org/10.1126/science.aad2035openalex-snapshot

Hobit and Blimp1 instruct a universal transcriptional program of tissue residency in lymphocytes

inferredcites →https://doi.org/10.1126/sciimmunol.aag2031openalex-snapshot

Dynamics of influenza-induced lung-resident memory T cells underlie waning heterosubtypic immunity

inferredcites →https://doi.org/10.1126/sciimmunol.aaj1996openalex-snapshot

Up-regulation of LFA-1 allows liver-resident memory T cells to patrol and remain in the hepatic sinusoids

inferredcites →https://doi.org/10.1126/sciimmunol.aam6970openalex-snapshot

Resident memory CD8 + T cells in the upper respiratory tract prevent pulmonary influenza virus infection

inferredcites →https://doi.org/10.1126/sciimmunol.aan6049openalex-snapshot

Enzymatic synthesis of core 2 O-glycans governs the tissue-trafficking potential of memory CD8 + T cells

inferredcites →https://doi.org/10.1126/scitranslmed.aaa3700openalex-snapshot

Long-lasting stem cell–like memory CD8 + T cells with a naïve-like profile upon yellow fever vaccination

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/10.1146/annurev.immunol.25.022106.141548openalex-snapshot

Effector and Memory CTL Differentiation

inferredcites →https://doi.org/10.1182/blood-2004-11-4353openalex-snapshot

Disparate lymphoid chemokine expression in mice and men: no evidence of CCL21 synthesis by human high endothelial venules

inferredcites →https://doi.org/10.1371/journal.ppat.1007633openalex-snapshot

Central memory CD8+ T cells become CD69+ tissue-residents during viral skin infection independent of CD62L-mediated lymph node surveillance

inferredcites →https://doi.org/10.2217/imt.11.100openalex-snapshot

Naive, Effector and Memory CD8 T-cell Trafficking: Parallels and Distinctions

inferredcites →https://doi.org/10.3389/fimmu.2019.00351openalex-snapshot

Local Antigen Encounter Is Essential for Establishing Persistent CD8+ T-Cell Memory in the CNS

inferredcites →https://doi.org/10.3389/fimmu.2019.00733openalex-snapshot

Establishment and Maintenance of Conventional and Circulation-Driven Lung-Resident Memory CD8+ T Cells Following Respiratory Virus Infections

inferredcites →https://doi.org/10.4049/jimmunol.1000094openalex-snapshot

Kruppel-Like Factor 2 Is Required for Trafficking but Not Quiescence in Postactivated T Cells

inferredcites →https://doi.org/10.4049/jimmunol.1000492openalex-snapshot

Early Signals during CD8+ T Cell Priming Regulate the Generation of Central Memory Cells

inferredcites →https://doi.org/10.4049/jimmunol.1001421openalex-snapshot

Homeostatic Turnover of Virus-Specific Memory CD8 T Cells Occurs Stochastically and Is Independent of CD4 T Cell Help

inferredcites →https://doi.org/10.4049/jimmunol.1001948openalex-snapshot

Differential Localization of Effector and Memory CD8 T Cell Subsets in Lymphoid Organs during Acute Viral Infection

inferredcites →https://doi.org/10.4049/jimmunol.1201305openalex-snapshot

The Molecular Signature of Tissue Resident Memory CD8 T Cells Isolated from the Brain

inferredcites →https://doi.org/10.4049/jimmunol.1400003openalex-snapshot

Cutting Edge: Resident Memory CD8 T Cells Occupy Frontline Niches in Secondary Lymphoid Organs

inferredcites →https://doi.org/10.4049/jimmunol.1402058openalex-snapshot

IFN-γ Regulates CD8+ Memory T Cell Differentiation and Survival in Response to Weak, but Not Strong, TCR Signals

inferredcites →https://doi.org/10.4049/jimmunol.1402256openalex-snapshot

Cutting Edge: CD69 Interference with Sphingosine-1-Phosphate Receptor Function Regulates Peripheral T Cell Retention

inferredcites →https://doi.org/10.4049/jimmunol.1501521openalex-snapshot

Cutting Edge: Resident Memory CD8 T Cells Express High-Affinity TCRs

inferredcites →https://doi.org/10.4049/jimmunol.1502337openalex-snapshot

IL-15–Independent Maintenance of Tissue-Resident and Boosted Effector Memory CD8 T Cells

inferredcites →https://doi.org/10.4049/jimmunol.173.11.6694openalex-snapshot

Shortening the Infectious Period Does Not Alter Expansion of CD8 T Cells but Diminishes Their Capacity to Differentiate into Memory Cells

inferredcites →https://doi.org/10.4049/jimmunol.174.9.5341openalex-snapshot

Reducing the Stimulation of CD8+ T Cells during Infection with Intracellular Bacteria Promotes Differentiation Primarily into a Central (CD62LhighCD44high) Subset

inferredcites →https://doi.org/10.4049/jimmunol.175.7.4686openalex-snapshot

Functional Properties and Lineage Relationship of CD8+ T Cell Subsets Identified by Expression of IL-7 Receptor α and CD62L

inferredcites →https://doi.org/10.4049/jimmunol.176.4.2079openalex-snapshot

Cutting Edge: Gut Microenvironment Promotes Differentiation of a Unique Memory CD8 T Cell Population

inferredcites →https://doi.org/10.4049/jimmunol.177.11.7515openalex-snapshot

Cutting Edge: IL-12 Inversely Regulates T-bet and Eomesodermin Expression during Pathogen-Induced CD8+ T Cell Differentiation

inferredcites →https://doi.org/10.4049/jimmunol.177.2.831openalex-snapshot

Stimulation History Dictates Memory CD8 T Cell Phenotype: Implications for Prime-Boost Vaccination

inferredcites →https://doi.org/10.4049/jimmunol.178.12.7632openalex-snapshot

Kruppel-Like Factor 2 Controls T Cell Trafficking by Activating L-Selectin (CD62L) and Sphingosine-1-Phosphate Receptor 1 Transcription

inferredcites →https://doi.org/10.4049/jimmunol.179.1.53openalex-snapshot

Manipulating the Rate of Memory CD8+ T Cell Generation after Acute Infection

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The Impact of TCR Signal Strength on Resident Memory T Cell Formation during Influenza Virus Infection

What points at this work

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

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Additional file 1 of Characteristics of circulating immune cells in HBV-related acute-on-chronic liver failure following artificial liver treatment

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