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Heterogeneity and Cell-Fate Decisions in Effector and Memory CD8+ T Cell Differentiation during Viral Infection

https://doi.org/10.1016/j.immuni.2007.08.007

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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/eji.200324717openalex-snapshot

Maintenance of memory CTL responses by T helper cells and CD40‐CD40 ligand: antibodies provide the key

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/10.1016/j.coi.2004.03.004openalex-snapshot

Towards a cellular definition of CD8+ T-cell memory: the role of CD4+ T-cell help in CD8+ T-cell responses

inferredcites →https://doi.org/10.1016/j.coi.2004.05.004openalex-snapshot

CD8+ T-cell memory: only the good ones last

inferredcites →https://doi.org/10.1016/j.coi.2007.06.004openalex-snapshot

CD8 T cell dysfunction during chronic viral infection

inferredcites →https://doi.org/10.1016/j.immuni.2005.01.010openalex-snapshot

Peripheral Tolerance of CD8 T Lymphocytes

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.2007.08.010openalex-snapshot

Human Immunodeficiency Virus Controllers: Mechanisms of Durable Virus Control in the Absence of Antiretroviral Therapy

inferredcites →https://doi.org/10.1016/j.immuni.2007.08.012openalex-snapshot

Innate Recognition of Viruses

inferredcites →https://doi.org/10.1016/j.immuni.2007.09.002openalex-snapshot

Antibodies and B Cell Memory in Viral Immunity

inferredcites →https://doi.org/10.1016/j.virol.2006.06.017openalex-snapshot

HIV-specific CD8 T cells express low levels of IL-7Rα: Implications for HIV-specific T cell memory

inferredcites →https://doi.org/10.1016/s0092-8674(02)01139-xopenalex-snapshot

Molecular and Functional Profiling of Memory CD8 T Cell Differentiation

inferredcites →https://doi.org/10.1016/s1074-7613(00)80470-7openalex-snapshot

Counting Antigen-Specific CD8 T Cells: A Reevaluation of Bystander Activation during Viral Infection

inferredcites →https://doi.org/10.1038/35065111openalex-snapshot

Visualizing the generation of memory CD4 T cells in the whole body

inferredcites →https://doi.org/10.1038/35065118openalex-snapshot

Skewed maturation of memory HIV-specific CD8 T lymphocytes

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/10.1038/90950openalex-snapshot

Differential regulation of antiviral T-cell immunity results in stable CD8+ but declining CD4+ T-cell memory

inferredcites →https://doi.org/10.1038/nature03337openalex-snapshot

CD4+ T-cell help controls CD8+ T-cell memory via TRAIL-mediated activation-induced cell death

inferredcites →https://doi.org/10.1038/nature04444openalex-snapshot

Restoring function in exhausted CD8 T cells during chronic viral infection

inferredcites →https://doi.org/10.1038/nature04651openalex-snapshot

Chemokines enhance immunity by guiding naive CD8+ T cells to sites of CD4+ T cell–dendritic cell interaction

inferredcites →https://doi.org/10.1038/nature04790openalex-snapshot

Interleukin-2 signals during priming are required for secondary expansion of CD8+ memory T cells

inferredcites →https://doi.org/10.1038/nature05115openalex-snapshot

PD-1 expression on HIV-specific T cells is associated with T-cell exhaustion and disease progression

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/ni1227openalex-snapshot

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

inferredcites →https://doi.org/10.1038/ni1241openalex-snapshot

T cells and viral persistence: lessons from diverse infections

inferredcites →https://doi.org/10.1038/ni1268openalex-snapshot

Effector and memory CD8+ T cell fate coupled by T-bet and eomesodermin

inferredcites →https://doi.org/10.1038/ni832openalex-snapshot

Distinct lineages of TH1 cells have differential capacities for memory cell generation in vivo

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/ni908openalex-snapshot

T cell fitness determined by signal strength

inferredcites →https://doi.org/10.1038/ni969openalex-snapshot

Similarities and differences in CD4+ and CD8+ effector and memory T cell generation

inferredcites →https://doi.org/10.1038/nm0402-379openalex-snapshot

Memory CD8+ T cells vary in differentiation phenotype in different persistent virus infections

inferredcites →https://doi.org/10.1038/nm1257openalex-snapshot

Accelerated CD8+ T-cell memory and prime-boost response after dendritic-cell vaccination

inferredcites →https://doi.org/10.1038/nm1482openalex-snapshot

Upregulation of PD-1 expression on HIV-specific CD8+ T cells leads to reversible immune dysfunction

inferredcites →https://doi.org/10.1038/nm866openalex-snapshot

Therapeutic use of IL-2 to enhance antiviral T-cell responses in vivo

inferredcites →https://doi.org/10.1038/nri1254openalex-snapshot

Human CD8+ T-cell differentiation in response to viruses

inferredcites →https://doi.org/10.1038/nri1866openalex-snapshot

The descent of memory T-cell subsets

inferredcites →https://doi.org/10.1038/nri778openalex-snapshot

Effector and memory T-cell differentiation: implications for vaccine development

inferredcites →https://doi.org/10.1073/pnas.0308054101openalex-snapshot

Selective expression of IL-7 receptor on memory T cells identifies early CD40L-dependent generation of distinct CD8 + memory T cell subsets

inferredcites →https://doi.org/10.1073/pnas.0407192101openalex-snapshot

Antigen-independent memory CD8 T cells do not develop during chronic viral infection

inferredcites →https://doi.org/10.1073/pnas.0503726102openalex-snapshot

Central memory self/tumor-reactive CD8 + T cells confer superior antitumor immunity compared with effector memory T cells

inferredcites →https://doi.org/10.1073/pnas.0705007104openalex-snapshot

Expression of IL-7 receptor α is necessary but not sufficient for the formation of memory CD8 T cells during viral infection

inferredcites →https://doi.org/10.1073/pnas.101132698openalex-snapshot

Measuring the diaspora for virus-specific CD8 + T cells

inferredcites →https://doi.org/10.1084/jem.186.9.1407openalex-snapshot

Phenotypic and Functional Separation of Memory and Effector Human CD8+ T Cells

inferredcites →https://doi.org/10.1084/jem.189.8.1315openalex-snapshot

Two Roads Diverged: Interferon α/β– and Interleukin 12–mediated Pathways in Promoting T Cell Interferon γ Responses during Viral Infection

inferredcites →https://doi.org/10.1084/jem.20001021openalex-snapshot

Estimating the Precursor Frequency of Naive Antigen-specific CD8 T Cells

inferredcites →https://doi.org/10.1084/jem.20030725openalex-snapshot

IL-7 Promotes the Transition of CD4 Effectors to Persistent Memory Cells

inferredcites →https://doi.org/10.1084/jem.20030735openalex-snapshot

Interleukin 7 Regulates the Survival and Generation of Memory CD4 Cells

inferredcites →https://doi.org/10.1084/jem.20040876openalex-snapshot

Lineage relationships, homeostasis, and recall capacities of central– and effector–memory CD8 T cells in vivo

inferredcites →https://doi.org/10.1084/jem.20041463openalex-snapshot

Interferon-γ acts directly on CD8+ T cells to increase their abundance during virus infection

inferredcites →https://doi.org/10.1084/jem.20050137openalex-snapshot

Differential contributions of central and effector memory T cells to recall responses

inferredcites →https://doi.org/10.1084/jem.20050821openalex-snapshot

Type I interferons act directly on CD8 T cells to allow clonal expansion and memory formation in response to viral infection

inferredcites →https://doi.org/10.1084/jem.20051954openalex-snapshot

CD4+ T cells that enter the draining lymph nodes after antigen injection participate in the primary response and become central–memory cells

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.20052433openalex-snapshot

Toll-like receptor agonists influence the magnitude and quality of memory T cell responses after prime-boost immunization in nonhuman primates

inferredcites →https://doi.org/10.1084/jem.20060995openalex-snapshot

Continuous recruitment of naive T cells contributes to heterogeneity of antiviral CD8 T cells during persistent infection

inferredcites →https://doi.org/10.1084/jem.20061496openalex-snapshot

PD-1 is a regulator of virus-specific CD8+ T cell survival in HIV infection

inferredcites →https://doi.org/10.1084/jem.20061805openalex-snapshot

Antiviral CD4+ memory T cells are IL-15 dependent

inferredcites →https://doi.org/10.1084/jem.20061937openalex-snapshot

Viral antigen and extensive division maintain virus-specific CD8 T cells during chronic infection

inferredcites →https://doi.org/10.1084/jem.20062381openalex-snapshot

Interleukin-2 enhances CD4+ T cell memory by promoting the generation of IL-7Rα–expressing cells

inferredcites →https://doi.org/10.1084/jem.20070322openalex-snapshot

Activation phenotype, rather than central– or effector–memory phenotype, predicts the recall efficacy of memory CD8+ T cells

inferredcites →https://doi.org/10.1084/jem.20070841openalex-snapshot

Requirement for T-bet in the aberrant differentiation of unhelped memory CD8+ T cells

inferredcites →https://doi.org/10.1086/509510openalex-snapshot

Functionally Competent Antigen‐Specific CD127hiMemory CD8+T Cells Are Preserved Only in HIV‐Infected Individuals Receiving Early Treatment

inferredcites →https://doi.org/10.1097/01.aids.0000191919.24185.46openalex-snapshot

Modulation of interleukin-7 receptor expression characterizes differentiation of CD8 T cells specific for HIV, EBV and CMV

inferredcites →https://doi.org/10.1111/j.0105-2896.2006.00382.xopenalex-snapshot

Signals required for programming effector and memory development by CD8+ T cells

inferredcites →https://doi.org/10.1111/j.0105-2896.2006.00401.xopenalex-snapshot

Homeostasis of memory T cells

inferredcites →https://doi.org/10.1126/science.1058867openalex-snapshot

Preferential Localization of Effector Memory Cells in Nonlymphoid Tissue

inferredcites →https://doi.org/10.1126/science.1059835openalex-snapshot

Role of T-bet in Commitment of T H 1 Cells Before IL-12-Dependent Selection

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.272.5258.54openalex-snapshot

Immunological Memory and Protective Immunity: Understanding Their Relation

inferredcites →https://doi.org/10.1126/science.286.5441.958openalex-snapshot

A Direct Estimate of the Human αβ T Cell Receptor Diversity

inferredcites →https://doi.org/10.1126/science.290.5495.1354openalex-snapshot

Regulation of Antigen-Specific CD8 + T Cell Homeostasis by Perforin and Interferon-γ

inferredcites →https://doi.org/10.1128/jvi.02021-06openalex-snapshot

Liver-Infiltrating Lymphocytes in Chronic Human Hepatitis C Virus Infection Display an Exhausted Phenotype with High Levels of PD-1 and Low Levels of CD127 Expression

inferredcites →https://doi.org/10.1128/jvi.78.1.206-215.2004openalex-snapshot

Subsets of Memory Cytotoxic T Lymphocytes Elicited by Vaccination Influence the Efficiency of Secondary Expansion In Vivo

inferredcites →https://doi.org/10.1128/jvi.78.11.5535-5545.2004openalex-snapshot

Memory CD8 T-Cell Differentiation during Viral Infection

inferredcites →https://doi.org/10.1146/annurev.immunol.14.1.333openalex-snapshot

ON IMMUNOLOGICAL MEMORY

inferredcites →https://doi.org/10.1146/annurev.immunol.18.1.83openalex-snapshot

Population Biology of Lymphocytes: The Flight for Survival

inferredcites →https://doi.org/10.1146/annurev.immunol.23.021704.115611openalex-snapshot

THE B7 FAMILY REVISITED

inferredcites →https://doi.org/10.1146/annurev.immunol.23.021704.115839openalex-snapshot

TNF/TNFR FAMILY MEMBERS IN COSTIMULATION OF T CELL RESPONSES

inferredcites →https://doi.org/10.1146/annurev.immunol.25.022106.141548openalex-snapshot

Effector and Memory CTL Differentiation

inferredcites →https://doi.org/10.1172/jci13296openalex-snapshot

Effector differentiation is not prerequisite for generation of memory cytotoxic T lymphocytes

inferredcites →https://doi.org/10.1172/jci14005openalex-snapshot

Exploring pathways for memory T cell generation

inferredcites →https://doi.org/10.1172/jci23134openalex-snapshot

Adjuvant IL-7 or IL-15 overcomes immunodominance and improves survival of the CD8+ memory cell pool

inferredcites →https://doi.org/10.1182/blood-2005-02-0449openalex-snapshot

IL-7 receptor α chain expression distinguishes functional subsets of virus-specific human CD8+ T cells

inferredcites →https://doi.org/10.1182/blood-2006-09-044826openalex-snapshot

PD-1 up-regulation is correlated with HIV-specific memory CD8+ T-cell exhaustion in typical progressors but not in long-term nonprogressors

inferredcites →https://doi.org/10.1182/blood-2006-10-053256openalex-snapshot

TLR3 ligand stimulates fully functional memory CD8+ T cells in the absence of CD4+ T-cell help

inferredcites →https://doi.org/10.1182/blood.v98.6.1667openalex-snapshot

Dressed to kill? A review of why antiviral CD8 T lymphocytes fail to prevent progressive immunodeficiency in HIV-1 infection

inferredcites →https://doi.org/10.4049/jimmunol.152.4.1653openalex-snapshot

Heterosubtypic immunity to influenza type A virus in mice. Effector mechanisms and their longevity.

inferredcites →https://doi.org/10.4049/jimmunol.160.2.535openalex-snapshot

Cutting Edge Commentary: Differential TCR Signaling and the Generation of Memory T Cells

inferredcites →https://doi.org/10.4049/jimmunol.163.7.3735openalex-snapshot

The Induction of Virus-Specific CTL as a Function of Increasing Epitope Expression: Responses Rise Steadily Until Excessively High Levels of Epitope Are Attained

inferredcites →https://doi.org/10.4049/jimmunol.164.5.2354openalex-snapshot

The Density of Peptides Displayed by Dendritic Cells Affects Immune Responses to Human Tyrosinase and gp100 in HLA-A2 Transgenic Mice

inferredcites →https://doi.org/10.4049/jimmunol.166.3.1813openalex-snapshot

Activated Antigen-Specific CD8+ T Cells Persist in the Lungs Following Recovery from Respiratory Virus Infections

inferredcites →https://doi.org/10.4049/jimmunol.169.2.638openalex-snapshot

Cutting Edge: CCR7+ and CCR7− Memory T Cells Do Not Differ in Immediate Effector Cell Function

inferredcites →https://doi.org/10.4049/jimmunol.169.7.3760openalex-snapshot

Differential Sensitivity of Naive and Memory CD8+ T Cells to Apoptosis in Vivo

inferredcites →https://doi.org/10.4049/jimmunol.170.5.2461openalex-snapshot

Immediate Early Effector Functions of Virus-Specific CD8+CCR7+ Memory Cells in Humans Defined by HLA and CC Chemokine Ligand 19 Tetramers

inferredcites →https://doi.org/10.4049/jimmunol.171.1.27openalex-snapshot

Cutting Edge: Rapid In Vivo Killing by Memory CD8 T Cells

inferredcites →https://doi.org/10.4049/jimmunol.171.10.5165openalex-snapshot

CD8 T Cell Clonal Expansion and Development of Effector Function Require Prolonged Exposure to Antigen, Costimulation, and Signal 3 Cytokine

inferredcites →https://doi.org/10.4049/jimmunol.172.11.6533openalex-snapshot

Cutting Edge: Effector Memory CD8+ T Cells Play a Prominent Role in Recall Responses to Secondary Viral Infection in the Lung

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.174.11.6791openalex-snapshot

Dynamic Regulation of IFN-γ Signaling in Antigen-Specific CD8+ T Cells Responding to Infection

inferredcites →https://doi.org/10.4049/jimmunol.174.5.2900openalex-snapshot

Loss of CD127 Expression Defines an Expansion of Effector CD8+ T Cells in HIV-Infected Individuals

inferredcites →https://doi.org/10.4049/jimmunol.174.8.4465openalex-snapshot

Cutting Edge: Type I IFNs Provide a Third Signal to CD8 T Cells to Stimulate Clonal Expansion and Differentiation

inferredcites →https://doi.org/10.4049/jimmunol.175.6.3502openalex-snapshot

Vaccine-Induced CD8+ Central Memory T Cells in Protection from Simian AIDS

inferredcites →https://doi.org/10.4049/jimmunol.175.7.4400openalex-snapshot

IL-7 Receptor Expression Levels Do Not Identify CD8+ Memory T Lymphocyte Precursors following Peptide Immunization

inferredcites →https://doi.org/10.4049/jimmunol.175.7.4677openalex-snapshot

Recall Proliferation Potential of Memory CD8+ T Cells and Antiviral Protection

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.175.9.5624openalex-snapshot

Cutting Edge: Early IFN-γ Signaling Directly Enhances Primary Antiviral CD4+ T Cell Responses

inferredcites →https://doi.org/10.4049/jimmunol.176.5.3028openalex-snapshot

Precursor Frequency, Nonlinear Proliferation, and Functional Maturation of Virus-Specific CD4+ T Cells

inferredcites →https://doi.org/10.4049/jimmunol.177.1.511openalex-snapshot

Persistence and Function of Central and Effector Memory CD4+ T Cells following Infection with a Gastrointestinal Helminth

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.177.2.777openalex-snapshot

Cutting Edge: Latecomer CD8 T Cells Are Imprinted with a Unique Differentiation Program

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.177.2.999openalex-snapshot

TRAIL Deficiency Delays, but Does Not Prevent, Erosion in the Quality of “Helpless” Memory CD8 T Cells

inferredcites →https://doi.org/10.4049/jimmunol.177.7.4247openalex-snapshot

Cutting Edge: IL-7-Independent Regulation of IL-7 Receptor α Expression and Memory CD8 T Cell Development

inferredcites →https://doi.org/10.4049/jimmunol.177.7.4458openalex-snapshot

Augmented IL-7 Signaling during Viral Infection Drives Greater Expansion of Effector T Cells but Does Not Enhance Memory

inferredcites →https://doi.org/10.4049/jimmunol.178.12.7563openalex-snapshot

Persistent Depots of Influenza Antigen Fail To Induce a Cytotoxic CD8 T Cell Response

inferredcites →https://doi.org/10.4049/jimmunol.178.2.778openalex-snapshot

Chemokine-Guided CD4+ T Cell Help Enhances Generation of IL-6RαhighIL-7Rαhigh Prememory CD8+ T Cells

inferredcites →https://doi.org/10.4049/jimmunol.178.7.4027openalex-snapshot

Cutting Edge: Limiting Amounts of IL-7 Do Not Control Contraction of CD4+ T Cell Responses

inferredcites →https://doi.org/10.4049/jimmunol.178.7.4498openalex-snapshot

IL-12 and Type-I IFN Synergize for IFN-γ Production by CD4 T Cells, Whereas Neither Are Required for IFN-γ Production by CD8 T Cells after Listeria monocytogenes Infection

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

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

inferredcites →https://doi.org/10.4049/jimmunol.179.4.2074openalex-snapshot

Generation of CD8 T Cell Memory Is Regulated by IL-12

What points at this work

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

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Targeted Localization of the Mother Centrosome in CD8 T Cells Undergoing Asymmetric Cell Division Promotes Memory Formation

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Single cell multiomic analysis of T cell exhaustion in vitro

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Efficacy of IL‐2‐ versus IL‐15‐stimulated CD8 T cells in adoptive immunotherapy

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Effector T‐cell differentiation during viral and bacterial infections: Role of direct IL‐12 signals for cell fate decision of CD8+ T cells

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Altered effector functions of virus‐specific and virus cross‐reactive CD8+ T cells in mice immunized with related flaviviruses

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Parenchymal cells critically curtail cytotoxic T‐cell responses by inducing Bim‐mediated apoptosis

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Secondary CD8 + T‐cell responses are controlled by systemic inflammation

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T‐cell help permits memory CD8+ T‐cell inflation during cytomegalovirus latency

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Expansion of a restricted residual host Treg‐cell repertoire is dependent on IL‐2 following experimental autologous hematopoietic stem transplantation

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DOCK8 is essential for T‐cell survival and the maintenance of CD8+ T‐cell memory

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Tumor‐induced myeloid‐derived suppressor cell subsets exert either inhibitory or stimulatory effects on distinct CD 8 + T ‐cell activation events

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Novel molecular mechanism for generating NK‐cell fitness and memory

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Hobit and human effector T‐cell differentiation: The beginning of a long journey

inferred← citeshttps://doi.org/10.1002/eji.201747174openalex-snapshot

TCR‐pMHC encounter differentially regulates transcriptomes of tissue‐resident CD8 T cells

inferred← citeshttps://doi.org/10.1002/eji.201847897openalex-snapshot

Expression of IL‐7Rα and KLRG1 defines functionally distinct CD8 + T‐cell populations in humans

inferred← citeshttps://doi.org/10.1002/eji.202249918openalex-snapshot

Memory CD8 + T cells upregulate glycolysis and effector functions under limiting oxygen conditions

inferred← citeshttps://doi.org/10.1002/iid3.17openalex-snapshot

Human T cells expressing BEND3 on their surface represent a novel subpopulation that preferentially produces IL‐6 and IL‐8

inferred← citeshttps://doi.org/10.1002/iid3.221openalex-snapshot

Reactive glia promote development of CD103+CD69+ CD8+ T‐cells through programmed cell death‐ligand 1 (PD‐L1)

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Decoupling CAR‐T Expansion, Conversion, and Decay Timing: Physiologically Aligned Semi‐Mechanistic Modeling With Smooth Gating and a Cauchy Likelihood Residual Model

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A spatial view of the CD8+ T‐cell response: the case of HCV

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Sex differences in CD8 + T cell responses during adaptive immunity

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Memory CD4 T Cells in Influenza

inferred← citeshttps://doi.org/10.1007/978-1-0716-1884-4_3openalex-snapshot

Revisiting the Principles of Designing a Vaccine

inferred← citeshttps://doi.org/10.1007/978-1-4419-5632-3_8openalex-snapshot

Blimp1: Driving Terminal Differentiation to a T

inferred← citeshttps://doi.org/10.1007/978-1-4419-6451-9_11openalex-snapshot

Memory T-Cell Subsets in Parasitic Infections

inferred← citeshttps://doi.org/10.1007/978-1-62703-290-2_13openalex-snapshot

Isolation of RNA and the Synthesis and Amplification of cDNA from Antigen-Specific T Cells for Genome-Wide Expression Analysis

inferred← citeshttps://doi.org/10.1007/978-3-319-53661-3_2openalex-snapshot

Nonmelanoma Skin Cancer Actinic Keratosis and Squamous Cell Carcinoma

inferred← citeshttps://doi.org/10.1007/978-3-319-72317-4_7openalex-snapshot

Multi-scale and Integrative Modelling Approaches

inferred← citeshttps://doi.org/10.1007/978-94-024-1170-6_3openalex-snapshot

Transcriptional Regulation of T Cell Metabolism Reprograming

inferred← citeshttps://doi.org/10.1007/s00018-010-0362-2openalex-snapshot

The persistence of T cell memory

inferred← citeshttps://doi.org/10.1007/s00018-016-2211-4openalex-snapshot

Mechanisms of T cell organotropism

inferred← citeshttps://doi.org/10.1007/s00018-024-05423-9openalex-snapshot

Role of lamin A/C on dendritic cell function in antiviral immunity

inferred← citeshttps://doi.org/10.1007/s00262-010-0922-1openalex-snapshot

CD4+ T cell response against a non-tumor antigen is unaffected in melanoma-bearing mice

inferred← citeshttps://doi.org/10.1007/s00262-014-1633-9openalex-snapshot

Development of photodynamic therapy regimens that control primary tumor growth and inhibit secondary disease

inferred← citeshttps://doi.org/10.1007/s00281-018-0686-9openalex-snapshot

Memory responses of innate lymphocytes and parallels with T cells

inferred← citeshttps://doi.org/10.1007/s10620-014-3297-xopenalex-snapshot

Decreases in Activated CD8+ T Cells in Patients with Severe Hepatitis B Are Related to Outcomes

inferred← citeshttps://doi.org/10.1007/s10875-022-01379-2openalex-snapshot

Interferon-Driven Immune Dysregulation in Common Variable Immunodeficiency–Associated Villous Atrophy and Norovirus Infection

inferred← citeshttps://doi.org/10.1007/s12026-008-8027-zopenalex-snapshot

Intrinsic and extrinsic control of effector T cell survival and memory T cell development

inferred← citeshttps://doi.org/10.1007/s12026-022-09353-1openalex-snapshot

Regulation of effector and memory CD8 + T cell differentiation: a focus on orphan nuclear receptor NR4A family, transcription factor, and metabolism

inferred← citeshttps://doi.org/10.1007/s12190-026-02770-7openalex-snapshot

Neural network assisted stability exploration of a stochastic Hepatitis B model incorporating dual transmission routes and immune response

inferred← citeshttps://doi.org/10.1007/s13402-025-01040-1openalex-snapshot

Tumor-specific CXCR6 positive precursor CD8+ T cells mediate tumor control in metastatic melanoma

inferred← citeshttps://doi.org/10.1016/b978-0-12-374279-7.08013-9openalex-snapshot

Transition of T Cells from Effector to Memory Phase

inferred← citeshttps://doi.org/10.1016/b978-0-12-404734-1.00012-7openalex-snapshot

Distinct Cellular Targets of SIV Infection in Natural and Non-natural Hosts of SIV

inferred← citeshttps://doi.org/10.1016/b978-0-12-415847-4.00076-8openalex-snapshot

Simian Immunodeficiency Virus Infection and Mucosal Immunity

inferred← citeshttps://doi.org/10.1016/b978-0-12-802585-7.00003-0openalex-snapshot

Costimulation Immunotherapy in Infectious Diseases

inferred← citeshttps://doi.org/10.1016/b978-0-12-824465-4.00279-9openalex-snapshot

The Development of Activated CD8 T Cells During Transition From Effector to Memory Phases

inferred← citeshttps://doi.org/10.1016/b978-0-443-06668-9.50041-7openalex-snapshot

Tuberculosis and Atypical Mycobacterial Infections

inferred← citeshttps://doi.org/10.1016/b978-0-7020-3935-5.00035-5openalex-snapshot

Tuberculosis and Atypical Mycobacterial Infections

inferred← citeshttps://doi.org/10.1016/b978-1-4160-5569-3.50016-0openalex-snapshot