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Homeostasis of Naive and Memory T Cells
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1 of the 135 references listed on this page is in the Retraction Watch database as retracted (export 2026-11-04): 10.1074/jbc.m610036200 (notice 2011-02-18).
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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.1830160616openalex-snapshot
Autonomous activation of B and T cells in antigen‐free mice
inferredcites →https://doi.org/10.1002/eji.200737585openalex-snapshot
Non‐redundant role for IL‐7R signaling for the survival of CD8+ memory T cells
inferredcites →https://doi.org/10.1006/smim.1997.0091openalex-snapshot
Restoration of T-cell homeostasis after T-cell depletion
inferredcites →https://doi.org/10.1016/0092-8674(93)80065-mopenalex-snapshot
Bcl-2-deficient mice demonstrate fulminant lymphoid apoptosis, polycystic kidneys, and hypopigmented hair
inferredcites →https://doi.org/10.1016/j.cell.2007.03.008openalex-snapshot
miR-181a Is an Intrinsic Modulator of T Cell Sensitivity and Selection
inferredcites →https://doi.org/10.1016/j.immuni.2004.07.016openalex-snapshot
Suppression of IL7Rα Transcription by IL-7 and Other Prosurvival Cytokines
inferredcites →https://doi.org/10.1016/j.immuni.2007.07.007openalex-snapshot
Naive CD4+ T Cell Frequency Varies for Different Epitopes and Predicts Repertoire Diversity and Response Magnitude
inferredcites →https://doi.org/10.1016/j.immuni.2007.11.023openalex-snapshot
The Lupus-Related Lmb3 Locus Contains a Disease-Suppressing Coronin-1A Gene Mutation
inferredcites →https://doi.org/10.1016/j.immuni.2008.02.014openalex-snapshot
Rapid Culling of the CD4+ T Cell Repertoire in the Transition from Effector to Memory
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.smim.2005.02.007openalex-snapshot
Regulation of mature T cell homeostasis
inferredcites →https://doi.org/10.1016/j.smim.2007.04.003openalex-snapshot
A role for “self” in T-cell activation
inferredcites →https://doi.org/10.1016/j.tcb.2008.01.007openalex-snapshot
How do BCL-2 proteins induce mitochondrial outer membrane permeabilization?
inferredcites →https://doi.org/10.1016/s0092-8674(00)81444-0openalex-snapshot
Stat5a and Stat5b Proteins Have Essential and Nonessential, or Redundant, Roles in Cytokine Responses
inferredcites →https://doi.org/10.1016/s1074-7613(00)80055-2openalex-snapshot
Designing and Maintaining the Mature TCR Repertoire
inferredcites →https://doi.org/10.1016/s1074-7613(00)80092-8openalex-snapshot
The Peptide Ligands Mediating Positive Selection in the Thymus Control T Cell Survival and Homeostatic Proliferation in the Periphery
inferredcites →https://doi.org/10.1016/s1074-7613(00)80093-xopenalex-snapshot
Low-Affinity Ligands for the TCR Drive Proliferation of Mature CD8+ T Cells in Lymphopenic Hosts
inferredcites →https://doi.org/10.1016/s1074-7613(00)80317-9openalex-snapshot
MHC Class II Molecules Are Not Required for Survival of Newly Generated CD4+ T Cells, but Affect Their Long-Term Life Span
inferredcites →https://doi.org/10.1016/s1074-7613(00)80389-1openalex-snapshot
An Indirect Effect of Stat5a in IL-2–Induced Proliferation: A Critical Role for Stat5a in IL-2–Mediated IL-2 Receptor α Chain Induction
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/10.1016/s1074-7613(00)80664-0openalex-snapshot
IL-15 Receptor Maintains Lymphoid Homeostasis by Supporting Lymphocyte Homing and Proliferation
inferredcites →https://doi.org/10.1016/s1074-7613(01)00170-4openalex-snapshot
How Much TCR Does a T Cell Need?
inferredcites →https://doi.org/10.1016/s1074-7613(02)00429-6openalex-snapshot
IL-15Rα Recycles and Presents IL-15 In trans to Neighboring Cells
inferredcites →https://doi.org/10.1016/s1074-7613(02)00508-3openalex-snapshot
Neonates Support Lymphopenia-Induced Proliferation
inferredcites →https://doi.org/10.1016/s1074-7613(03)00078-5openalex-snapshot
Suppressor of Cytokine Signaling-1 Is a Critical Regulator of Interleukin-7-Dependent CD8+ T Cell Differentiation
inferredcites →https://doi.org/10.1016/s1074-7613(03)00356-xopenalex-snapshot
Plasticity of T Cell Memory Responses to Viruses
inferredcites →https://doi.org/10.1016/s1471-4906(01)02028-2openalex-snapshot
Interleukin-7: master regulator of peripheral T-cell homeostasis?
inferredcites →https://doi.org/10.1016/s1534-5807(01)00083-1openalex-snapshot
Degenerative Disorders Caused by Bcl-2 Deficiency Prevented by Loss of Its BH3-Only Antagonist Bim
inferredcites →https://doi.org/10.1038/35105066openalex-snapshot
Cytokines and immunodeficiency diseases
inferredcites →https://doi.org/10.1038/76917openalex-snapshot
γ chain required for naïve CD4+ T cell survival but not for antigen proliferation
inferredcites →https://doi.org/10.1038/79783openalex-snapshot
CD4+ T cell survival is not directly linked to self-MHC–induced TCR signaling
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/10.1038/90950openalex-snapshot
Differential regulation of antiviral T-cell immunity results in stable CD8+ but declining CD4+ T-cell memory
inferredcites →https://doi.org/10.1038/nature02067openalex-snapshot
Development and maintenance of B and T lymphocytes requires antiapoptotic MCL-1
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/nature04882openalex-snapshot
Kruppel-like factor 2 regulates thymocyte and T-cell migration
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/ni1105openalex-snapshot
CD4+ T cells are required for the maintenance, not programming, of memory CD8+ T cells after acute infection
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/ni1326openalex-snapshot
The generation of protective memory-like CD8+ T cells during homeostatic proliferation requires CD4+ T cells
inferredcites →https://doi.org/10.1038/ni1418openalex-snapshot
B and T lymphocyte attenuator regulates CD8+ T cell–intrinsic homeostasis and memory cell generation
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/ni1514openalex-snapshot
COP9 signalosome subunit 8 is essential for peripheral T cell homeostasis and antigen receptor–induced entry into the cell cycle from quiescence
inferredcites →https://doi.org/10.1038/ni1565openalex-snapshot
Transcription factor KLF2 regulates the migration of naive T cells by restricting chemokine receptor expression patterns
inferredcites →https://doi.org/10.1038/ni1570openalex-snapshot
Regulation of T cell survival through coronin-1–mediated generation of inositol-1,4,5-trisphosphate and calcium mobilization after T cell receptor triggering
inferredcites →https://doi.org/10.1038/ni766openalex-snapshot
Impairment of immunological memory in the absence of MHC despite survival of memory 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/ni946openalex-snapshot
Interleukin 7 and T cell receptor signals regulate homeostasis of CD4 memory cells
inferredcites →https://doi.org/10.1038/nm1710openalex-snapshot
IL-22 mediates mucosal host defense against Gram-negative bacterial pneumonia
inferredcites →https://doi.org/10.1038/nm1720openalex-snapshot
Interleukin-22 mediates early host defense against attaching and effacing bacterial pathogens
inferredcites →https://doi.org/10.1038/nri2023openalex-snapshot
Interleukin-7 receptor expression: intelligent design
inferredcites →https://doi.org/10.1038/nri2093openalex-snapshot
SOCS proteins, cytokine signalling and immune regulation
inferredcites →https://doi.org/10.1038/nri2251openalex-snapshot
Shaping and reshaping CD8+ T-cell memory
inferredcites →https://doi.org/10.1038/nri853openalex-snapshot
Maintaining the norm: T-cell homeostasis
inferredcites →https://doi.org/10.1038/nri931openalex-snapshot
Lymphocide: cytokines and the control of lymphoid homeostasis
inferredcites →https://doi.org/10.1038/nrm1660openalex-snapshot
Autophagy in metazoans: cell survival in the land of plenty
inferredcites →https://doi.org/10.1073/pnas.0334572100openalex-snapshot
Competition for self ligands restrains homeostatic proliferation of naive CD4 T cells
inferredcites →https://doi.org/10.1073/pnas.0400640101openalex-snapshot
IL-7 regulates basal homeostatic proliferation of antiviral CD4 + T cell memory
inferredcites →https://doi.org/10.1073/pnas.0407417101openalex-snapshot
The molecular program induced in T cells undergoing homeostatic proliferation
inferredcites →https://doi.org/10.1073/pnas.0507350103openalex-snapshot
Stat5a/b are essential for normal lymphoid development and differentiation
inferredcites →https://doi.org/10.1073/pnas.0737048100openalex-snapshot
IL-15Rα expression on CD8 + T cells is dispensable for T cell memory
inferredcites →https://doi.org/10.1073/pnas.1037754100openalex-snapshot
On the role of MHC class II molecules in the survival and lymphopenia-induced proliferation of peripheral CD4 + T cells
inferredcites →https://doi.org/10.1073/pnas.141218898openalex-snapshot
How αβ T cells deal with induced TCRα ablation
inferredcites →https://doi.org/10.1073/pnas.161126098openalex-snapshot
IL-7 is critical for homeostatic proliferation and survival of naïve T cells
inferredcites →https://doi.org/10.1073/pnas.212214999openalex-snapshot
IL-2 negatively regulates IL-7 receptor α chain expression in activated T lymphocytes
inferredcites →https://doi.org/10.1074/jbc.m610036200openalex-snapshot
Soluble Interleukin (IL)-15Rα Is Generated by Alternative Splicing or Proteolytic Cleavage and Forms Functional Complexes with IL-15
inferredcites →https://doi.org/10.1084/jem.179.4.1127openalex-snapshot
Turnover of naive- and memory-phenotype T cells.
inferredcites →https://doi.org/10.1084/jem.181.4.1519openalex-snapshot
Lymphopenia in interleukin (IL)-7 gene-deleted mice identifies IL-7 as a nonredundant cytokine.
inferredcites →https://doi.org/10.1084/jem.185.12.2089openalex-snapshot
T Cell Stimulation In Vivo by Lipopolysaccharide (LPS)
inferredcites →https://doi.org/10.1084/jem.188.11.2067openalex-snapshot
Stat5b Is Essential for Natural Killer Cell–mediated Proliferation and Cytolytic Activity
inferredcites →https://doi.org/10.1084/jem.191.5.771openalex-snapshot
Reversible Defects in Natural Killer and Memory Cd8 T Cell Lineages in Interleukin 15–Deficient Mice
inferredcites →https://doi.org/10.1084/jem.193.2.219openalex-snapshot
Fatal Leukemia in Interleukin 15 Transgenic Mice Follows Early Expansions in Natural Killer and Memory Phenotype Cd8+ T Cells
inferredcites →https://doi.org/10.1084/jem.194.8.1187openalex-snapshot
T Cell–Independent Interleukin 15rα Signals Are Required for Bystander Proliferation
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.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.20020067openalex-snapshot
Overexpression of Interleukin (IL)-7 Leads to IL-15–independent Generation of Memory Phenotype CD8+ T 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.20020772openalex-snapshot
Interleukin 15 Controls both Proliferation and Survival of a Subset of Memory-Phenotype CD8+ T Cells
inferredcites →https://doi.org/10.1084/jem.20021812openalex-snapshot
Involvement of Avidity for Major Histocompatibility Complex in Homeostasis of Naive and Memory 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.20030963openalex-snapshot
Are Major Histocompatibility Complex Molecules Involved in the Survival of Naive CD4+ T Cells?
inferredcites →https://doi.org/10.1084/jem.20040779openalex-snapshot
CD24 Expression on T Cells Is Required for Optimal T Cell Proliferation in Lymphopenic Host
inferredcites →https://doi.org/10.1084/jem.20041389openalex-snapshot
Coordinate Expression and Trans Presentation of Interleukin (IL)-15Rα and IL-15 Supports Natural Killer Cell and Memory CD8+ T Cell Homeostasis
inferredcites →https://doi.org/10.1084/jem.20050003openalex-snapshot
SOCS-1 regulates IL-15–driven homeostatic proliferation of antigen-naive CD8 T cells, limiting their autoimmune potential
inferredcites →https://doi.org/10.1084/jem.20052293openalex-snapshot
Massive and destructive T cell response to homeostatic cue in CD24-deficient lymphopenic hosts
inferredcites →https://doi.org/10.1084/jem.20052495openalex-snapshot
A major histocompatibility complex class I–dependent subset of memory phenotype CD8+ cells
inferredcites →https://doi.org/10.1084/jem.20061303openalex-snapshot
A critical role for the autophagy gene Atg5 in T cell survival and proliferation
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.20061871openalex-snapshot
Impaired CD8 T cell memory and CD4 T cell primary responses in IL-7Rα mutant mice
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.20070618openalex-snapshot
Bim/Bcl-2 balance is critical for maintaining naive and memory T cell homeostasis
inferredcites →https://doi.org/10.1084/jem.20070740openalex-snapshot
An intense form of homeostatic proliferation of naive CD8+ cells driven by IL-2
inferredcites →https://doi.org/10.1101/gad.13.12.1501openalex-snapshot
CDK inhibitors: positive and negative regulators of G1-phase progression
inferredcites →https://doi.org/10.1111/j.0105-2896.2006.00383.xopenalex-snapshot
Not all CD4+ memory T cells are long lived
inferredcites →https://doi.org/10.1111/j.0105-2896.2006.00423.xopenalex-snapshot
Regulatory T cells suppress systemic and mucosal immune activation to control intestinal inflammation
inferredcites →https://doi.org/10.1126/science.1122927openalex-snapshot
Selective Stimulation of T Cell Subsets with Antibody-Cytokine Immune Complexes
inferredcites →https://doi.org/10.1126/science.1124228openalex-snapshot
Naïve and Memory CD4 + T Cell Survival Controlled by Clonal Abundance
inferredcites →https://doi.org/10.1126/science.1130563openalex-snapshot
Requirement for Coronin 1 in T Lymphocyte Trafficking and Cellular Homeostasis
inferredcites →https://doi.org/10.1126/science.272.5270.1947openalex-snapshot
Induction of Bystander T Cell Proliferation by Viruses and Type I Interferon in Vivo
inferredcites →https://doi.org/10.1126/science.276.5321.2057openalex-snapshot
Differential Requirements for Survival and Proliferation of CD8 Naïve or Memory T Cells
inferredcites →https://doi.org/10.1126/science.277.5334.1986openalex-snapshot
LKLF: A Transcriptional Regulator of Single-Positive T Cell Quiescence and Survival
inferredcites →https://doi.org/10.1126/science.286.5443.1381openalex-snapshot
Class II-Independent Generation of CD4 Memory T Cells from Effectors
inferredcites →https://doi.org/10.1126/science.7542801openalex-snapshot
A Role for CD5 in TCR-Mediated Signal Transduction and Thymocyte Selection
inferredcites →https://doi.org/10.1128/mcb.24.14.6501-6513.2004openalex-snapshot
Distinct Regions of the Interleukin-7 Receptor Regulate Different Bcl2 Family Members
inferredcites →https://doi.org/10.1146/annurev.immunol.20.100101.151926openalex-snapshot
T Cell Memory
inferredcites →https://doi.org/10.1146/annurev.immunol.21.120601.141107openalex-snapshot
Positive and Negative Selection of T Cells
inferredcites →https://doi.org/10.1146/annurev.immunol.24.021605.090727openalex-snapshot
DIVERSE FUNCTIONS OF IL-2, IL-15, AND IL-7 IN LYMPHOID HOMEOSTASIS
inferredcites →https://doi.org/10.1172/jci13296openalex-snapshot
Effector differentiation is not prerequisite for generation of memory cytotoxic T lymphocytes
inferredcites →https://doi.org/10.1182/blood-2004-06-2484openalex-snapshot
Dynamic regulation of IL-7 receptor expression is required for normal thymopoiesis
inferredcites →https://doi.org/10.1182/blood-2006-04-016857openalex-snapshot
Do CD8 effector cells need IL-7R expression to become resting memory cells?
inferredcites →https://doi.org/10.4049/jimmunol.149.4.1204openalex-snapshot
Mice deprived of exogenous antigenic stimulation develop a normal repertoire of functional T cells
inferredcites →https://doi.org/10.4049/jimmunol.163.7.3793openalex-snapshot
Regulation of T Cell Homeostasis by Heparan Sulfate-Bound IL-2
inferredcites →https://doi.org/10.4049/jimmunol.166.4.2460openalex-snapshot
Autologous Regulation of Naive T Cell Homeostasis Within the T Cell Compartment
inferredcites →https://doi.org/10.4049/jimmunol.167.10.5664openalex-snapshot
Homeostatic Expansion Occurs Independently of Costimulatory Signals
inferredcites →https://doi.org/10.4049/jimmunol.167.12.6711openalex-snapshot
Cutting Edge: Secondary Lymphoid Organs Are Essential for Maintaining the CD4, But Not CD8, Naive T Cell Pool
inferredcites →https://doi.org/10.4049/jimmunol.169.6.2997openalex-snapshot
TCR Signals Mediated by Src Family Kinases Are Essential for the Survival of Naive T Cells
inferredcites →https://doi.org/10.4049/jimmunol.169.7.3752openalex-snapshot
TCR and IL-7 Receptor Signals Can Operate Independently or Synergize to Promote Lymphopenia-Induced Expansion of Naive T Cells
inferredcites →https://doi.org/10.4049/jimmunol.170.10.5018openalex-snapshot
IL-15 Promotes the Survival of Naive and Memory Phenotype CD8+ T Cells
inferredcites →https://doi.org/10.4049/jimmunol.170.8.3939openalex-snapshot
Cutting Edge: Cure of Colitis by CD4+CD25+ Regulatory T Cells
inferredcites →https://doi.org/10.4049/jimmunol.172.1.40openalex-snapshot
A Role for TCR Affinity in Regulating Naive T Cell Homeostasis
inferredcites →https://doi.org/10.4049/jimmunol.172.6.3391openalex-snapshot
Suppression of CD4+ T Lymphocyte Effector Functions by CD4+CD25+ Cells In Vivo
inferredcites →https://doi.org/10.4049/jimmunol.173.10.6041openalex-snapshot
Evidence of a Novel IL-2/15Rβ-Targeted Cytokine Involved in Homeostatic Proliferation of Memory CD8+ T Cells
inferredcites →https://doi.org/10.4049/jimmunol.173.11.6537openalex-snapshot
Cutting Edge: Transpresentation of IL-15 by Bone Marrow-Derived Cells Necessitates Expression of IL-15 and IL-15Rα by the Same Cells
inferredcites →https://doi.org/10.4049/jimmunol.173.6.3909openalex-snapshot
A Role for CD28 in Lymphopenia-Induced Proliferation of CD4 T Cells
inferredcites →https://doi.org/10.4049/jimmunol.174.10.6039openalex-snapshot
Spontaneous and Homeostatic Proliferation of CD4 T Cells Are Regulated by Different Mechanisms
inferredcites →https://doi.org/10.4049/jimmunol.174.2.688openalex-snapshot
Negative Regulation of T Cell Homeostasis by Lymphocyte Activation Gene-3 (CD223)
inferredcites →https://doi.org/10.4049/jimmunol.174.6.3158openalex-snapshot
Cutting Edge: Recent Immune Status Determines the Source of Antigens That Drive Homeostatic T Cell Expansion
inferredcites →https://doi.org/10.4049/jimmunol.176.7.4029openalex-snapshot
Suppressor of Cytokine Signaling 1 Stringently Regulates Distinct Functions of IL-7 and IL-15 In Vivo during T Lymphocyte Development and Homeostasis
inferredcites →https://doi.org/10.4049/jimmunol.180.3.1634openalex-snapshot
Regulation of T Cell Homeostasis by the Transmembrane Adaptor Protein SIT
inferredcites →https://doi.org/10.4049/jimmunol.180.8.5320openalex-snapshot
The Lymphopenic Environment of CD132 (Common γ-Chain)-Deficient Hosts Elicits Rapid Homeostatic Proliferation of Naive T Cells via IL-15
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4628537openalex-extracted
Changes in Immune Cell Subtypes During Ageingchanges in Immune Cell Subtypes During Ageing
inferred← citeshttps://doi.org/10.1002/1878-0261.13691openalex-snapshot
Metabolic dialogues: regulators of chimeric antigen receptor T cell function in the tumor microenvironment
inferred← citeshttps://doi.org/10.1002/9781118345313.ch5openalex-snapshot
Immunologic Memory: T Cells in Humans
inferred← citeshttps://doi.org/10.1002/9781119072997.ch6openalex-snapshot
T cells and the principles of immune responses
inferred← citeshttps://doi.org/10.1002/9781444355628.ch1openalex-snapshot
The Immune Response to a Transplanted Organ: An Overview
inferred← citeshttps://doi.org/10.1002/9781444355628.ch3openalex-snapshot
The T Cell Response to Transplantation Antigens
inferred← citeshttps://doi.org/10.1002/advs.202302175openalex-snapshot
Cell Granularity Reflects Immune Cell Function and Enables Selection of Lymphocytes with Superior Attributes for Immunotherapy
inferred← citeshttps://doi.org/10.1002/cam4.2361openalex-snapshot
Significantly increased anti‐tumor activity of carcinoembryonic antigen‐specific chimeric antigen receptor T cells in combination with recombinant human IL‐12
inferred← citeshttps://doi.org/10.1002/cbin.11093openalex-snapshot
IL‐7 enhances the differentiation of adipose‐derived stem cells toward lymphatic endothelial cells through AKT signaling
inferred← citeshttps://doi.org/10.1002/cpt.621openalex-snapshot
Predicting CD4 T‐Cell Reconstitution Following Pediatric Hematopoietic Stem Cell Transplantation
inferred← citeshttps://doi.org/10.1002/cti2.1475openalex-snapshot
Improving thymus implantation for congenital athymia with interleukin‐7
inferred← citeshttps://doi.org/10.1002/cyto.a.22351openalex-snapshot
From “truly naïve” to “exhausted senescent” T cells: When markers predict functionality
inferred← citeshttps://doi.org/10.1002/eji.200839210openalex-snapshot
CD122+CD8+ Treg suppress vaccine‐induced antitumor immune responses in lymphodepleted mice
inferred← citeshttps://doi.org/10.1002/eji.200939330openalex-snapshot
Homeostatic proliferation of naïve CD8+ T cells depends on CD62L/L‐selectin‐mediated homing to peripheral LN
inferred← citeshttps://doi.org/10.1002/eji.200939427openalex-snapshot
T cells require Foxo1 to populate the peripheral lymphoid organs
inferred← citeshttps://doi.org/10.1002/eji.200939444openalex-snapshot
Homeostatic proliferation and survival of naïve and memory T cells
inferred← citeshttps://doi.org/10.1002/eji.200939500openalex-snapshot
Organization and maintenance of immunological memory by stroma niches
inferred← citeshttps://doi.org/10.1002/eji.201040575openalex-snapshot
A dynamic immunological synapse mediates homeostatic TCR‐dependent and ‐independent signaling
inferred← citeshttps://doi.org/10.1002/eji.201040577openalex-snapshot
Apoptosis regulators Fas and Bim synergistically control T‐lymphocyte homeostatic proliferation
inferred← citeshttps://doi.org/10.1002/eji.201040870openalex-snapshot
Hyaluronan binding identifies the most proliferative activated and memory T cells
inferred← citeshttps://doi.org/10.1002/eji.201141586openalex-snapshot
Autonomous and extrinsic regulation of thymopoiesis inhuman immune system (HIS) mice
inferred← citeshttps://doi.org/10.1002/eji.201141611openalex-snapshot
Expansion of a restricted residual host Treg‐cell repertoire is dependent on IL‐2 following experimental autologous hematopoietic stem transplantation
inferred← citeshttps://doi.org/10.1002/eji.201141759openalex-snapshot
DOCK8 is essential for T‐cell survival and the maintenance of CD8+ T‐cell memory
inferred← citeshttps://doi.org/10.1002/eji.201142205openalex-snapshot
From crucial to negligible: Functional CD 8+ T ‐cell responses and their dependence on CD 4+ T ‐cell help
inferred← citeshttps://doi.org/10.1002/eji.201343750openalex-snapshot
G imap3 and G imap5 cooperate to maintain T ‐cell numbers in the mouse
inferred← citeshttps://doi.org/10.1002/eji.201344238openalex-snapshot
IL‐15 regulates Bcl‐2 family members Bim and Mcl‐1 through JAK/STAT and PI3K/AKT pathways in T cells
inferred← citeshttps://doi.org/10.1002/eji.201444701openalex-snapshot
OX40 and IL‐7 play synergistic roles in the homeostatic proliferation of effector memory CD4+ T cells
inferred← citeshttps://doi.org/10.1002/eji.201445295openalex-snapshot
Memory CD8+ T cells colocalize with IL‐7+ stromal cells in bone marrow and rest in terms of proliferation and transcription
inferred← citeshttps://doi.org/10.1002/eji.201545689openalex-snapshot
A novel experimental model of Cryptococcus neoformans‐related immune reconstitution inflammatory syndrome (IRIS) provides insights into pathogenesis
inferred← citeshttps://doi.org/10.1002/eji.201545761openalex-snapshot
Innate and virtual memory T cells in man
inferred← citeshttps://doi.org/10.1002/eji.201545907openalex-snapshot
Mesenteric lymph nodes contribute to proinflammatory Th17‐cell generation during inflammation of the small intestine in mice
inferred← citeshttps://doi.org/10.1002/eji.201646389openalex-snapshot
Disentangling Tfr cells from Treg cells and Tfh cells: How to untie the Gordian knot
inferred← citeshttps://doi.org/10.1002/eji.201646540openalex-snapshot
Weakly self‐reactive T‐cell clones can homeostatically expand when present at low numbers
inferred← citeshttps://doi.org/10.1002/eji.201646599openalex-snapshot
Survival of mature T cells in the periphery is intrinsically dependent on GIMAP1 in mice
inferred← citeshttps://doi.org/10.1002/eji.201646745openalex-snapshot
Metabolic wiring of murine T cell and intraepithelial lymphocyte maintenance and activation
inferred← citeshttps://doi.org/10.1002/eji.201747063openalex-snapshot
Maintenance of CD8+ memory T lymphocytes in the spleen but not in the bone marrow is dependent on proliferation
inferred← citeshttps://doi.org/10.1002/eji.201747120openalex-snapshot
Differential requirements for IRF4 in the clonal expansion and homeostatic proliferation of naive and memory murine CD8+ T cells
inferred← citeshttps://doi.org/10.1002/eji.201948208openalex-snapshot
Tissue resident T cell memory or how the magnificent seven are chilling in the bone
inferred← citeshttps://doi.org/10.1002/eji.201948368openalex-snapshot
IL‐7 derived from lymph node fibroblastic reticular cells is dispensable for naive T cell homeostasis but crucial for central memory T cell survival
inferred← citeshttps://doi.org/10.1002/eji.202048788openalex-snapshot
CD5 levels define functionally heterogeneous populations of naïve human CD4 + T cells
inferred← citeshttps://doi.org/10.1002/eji.202049055openalex-snapshot
T cells at work: How post‐transcriptional mechanisms control T cell homeostasis and activation
inferred← citeshttps://doi.org/10.1002/eji.202049057openalex-snapshot
Human CD8 T‐stem cell memory subsets phenotypic and functional characterization are defined by expression of CD122 or CXCR3
inferred← citeshttps://doi.org/10.1002/eji.202350836openalex-snapshot
Trappc1 intrinsically prevents ferroptosis of naive T cells to avoid spontaneous autoinflammatory disease in mice
inferred← citeshttps://doi.org/10.1002/eji.70174openalex-snapshot
Going Virtual as a Memory‐Phenotype T Lymphocyte
inferred← citeshttps://doi.org/10.1002/emmm.201000096openalex-snapshot
DNA‐dependent protein kinase catalytic subunit mediates T‐cell loss in rheumatoid arthritis
inferred← citeshttps://doi.org/10.1002/hep.26334openalex-snapshot
Alcohol dehydrogenase–specific T-cell responses are associated with alcohol consumption in patients with alcohol-related cirrhosis
inferred← citeshttps://doi.org/10.1002/ibd.21384openalex-snapshot
Comparative analysis of the effects of anti-IL-6 receptor mAb and anti-TNF mAb treatment on CD4+ T-cell responses in murine colitis
inferred← citeshttps://doi.org/10.1002/ibd.23000openalex-snapshot
Lineage Targeted MHC-II Transgenic Mice Demonstrate the Role of Dendritic Cells in Bacterial-driven Colitis
inferred← citeshttps://doi.org/10.1002/ijc.29854openalex-snapshot
Patient‐individualized CD 8+ cytolytic T ‐cell therapy effectively combats minimal residual leukemia in immunodeficient mice
inferred← citeshttps://doi.org/10.1002/jbmr.1500openalex-snapshot
Role of T cells in ovariectomy induced bone loss—revisited
inferred← citeshttps://doi.org/10.1002/jbmr.1886openalex-snapshot
Do γδ T cells predict osteonecrosis of the jaw?
inferred← citeshttps://doi.org/10.1002/jev2.12075openalex-snapshot
Professional killers: The role of extracellular vesicles in the reciprocal interactions between natural killer, CD8+ cytotoxic T‐cells and tumour cells
inferred← citeshttps://doi.org/10.1002/jgm.2652openalex-snapshot
Comparison of three humanized mouse models for adoptive T cell transfer
inferred← citeshttps://doi.org/10.1002/jlb.1ab0618-214rrropenalex-snapshot
Endogenous co-expression of two T cell receptors promotes lymphopenia-induced proliferation via increased affinity for self-antigen
inferred← citeshttps://doi.org/10.1002/jlb.2ri0717-278ropenalex-snapshot
Biology of IL-2 and its therapeutic modulation: Mechanisms and strategies
inferred← citeshttps://doi.org/10.1002/jlb.5cova0721-392rropenalex-snapshot
Characterization of memory T cell subsets and common γ−chain cytokines in convalescent COVID-19 individuals
inferred← citeshttps://doi.org/10.1002/path.4574openalex-snapshot
CD47 deficiency ameliorates autoimmune nephritis in Faslpr mice by suppressing IgG autoantibody production
inferred← citeshttps://doi.org/10.1002/stem.2115openalex-snapshot
In Vitro T-Cell Generation From Adult, Embryonic, and Induced Pluripotent Stem Cells: Many Roads to One Destination
inferred← citeshttps://doi.org/10.1007/82_2013_319openalex-snapshot
Self-Peptides in TCR Repertoire Selection and Peripheral T Cell Function
inferred← citeshttps://doi.org/10.1007/978-0-387-84828-0_31openalex-snapshot
Bcl-2 Family Members and Lymphocyte Homeostasis
inferred← citeshttps://doi.org/10.1007/978-0-387-84828-0_562openalex-snapshot
B Cell Central Tolerance: Controlling Self-Reactive B Cells in the Bone Marrow
inferred← citeshttps://doi.org/10.1007/978-1-0716-3754-8_14openalex-snapshot
Phenotypic and Functional Characterization of Memory CD4+ and CD8+ T Cells After Antigenic Stimulation
inferred← citeshttps://doi.org/10.1007/978-1-0716-3754-8_3openalex-snapshot
T Cell Subsets and Immune Homeostasis
inferred← citeshttps://doi.org/10.1007/978-1-4419-5632-3_7openalex-snapshot
Strategies and Implications for Prime-Boost Vaccination to Generate Memory CD8 T Cells
inferred← citeshttps://doi.org/10.1007/978-1-4419-6451-9_7openalex-snapshot
CD8 T-Cell Memory Differentiation during Acute and Chronic Viral Infections
inferred← citeshttps://doi.org/10.1007/978-1-4419-7725-0_13openalex-snapshot
B Cell Strategies of Ag Recognition in a Stratified Immune System
inferred← citeshttps://doi.org/10.1007/978-1-4614-8809-5_6openalex-snapshot
Employing T Cell Homeostasis as an Antitumor Strategy
inferred← citeshttps://doi.org/10.1007/978-1-4939-1655-9_11openalex-snapshot
Thymic Education of Human T Cells and Regulatory T Cell Development in Humanized Mice
inferred← citeshttps://doi.org/10.1007/978-1-4939-1655-9_15openalex-snapshot
Maintenance and Function of Human CD8+ T Cells and NK Cells in Humanized Mice
inferred← citeshttps://doi.org/10.1007/978-1-62703-290-2_9openalex-snapshot
Homeostatic Proliferation of Mature T Cells
inferred← citeshttps://doi.org/10.1007/978-3-030-57204-4_4openalex-snapshot
Mechanistic Models of CD4 T Cell Homeostasis and Reconstitution in Health and Disease
inferred← citeshttps://doi.org/10.1007/978-3-030-72029-2_6openalex-snapshot
Dysregulation of Adaptive Immunity in Sjögren’s Syndrome
inferred← citeshttps://doi.org/10.1007/978-3-0346-0219-8_3openalex-snapshot
Thy(–im)munosenescence: The Ageing of the Thymus and Its Impact on the Immune System
inferred← citeshttps://doi.org/10.1007/978-3-0348-0522-3_5openalex-snapshot
Central Role of Th17 Cells in Adaptive Immune Responses
inferred← citeshttps://doi.org/10.1007/978-3-319-56192-9_12openalex-snapshot
Bone and the Immune System
inferred← citeshttps://doi.org/10.1007/978-3-319-64597-1_118-1openalex-snapshot
Mechanisms of Naive CD4+ T Cell Maintenance in the Elderly and Its Implications for Autoimmunity
inferred← citeshttps://doi.org/10.1007/978-3-319-64597-1_12-1openalex-snapshot
Changes of T Cell Receptor (TCR) αβ Repertoire in the Face of Aging and Persistent Infections
inferred← citeshttps://doi.org/10.1007/978-3-319-64597-1_80-1openalex-snapshot
Nonhuman Primate Models of Immunosenescence
inferred← citeshttps://doi.org/10.1007/978-3-319-64597-1_81-1openalex-snapshot
Age-Specific T Cell Homeostasis
inferred← citeshttps://doi.org/10.1007/978-3-319-99375-1_118openalex-snapshot
Mechanisms of Naive CD4+ T Cell Maintenance in the Elderly and Its Implications for Autoimmunity
inferred← citeshttps://doi.org/10.1007/978-3-319-99375-1_12openalex-snapshot
Changes of T Cell Receptor (TCR) αβ Repertoire in the Face of Aging and Persistent Infections
inferred← citeshttps://doi.org/10.1007/978-3-319-99375-1_80openalex-snapshot
Nonhuman Primate Models of Immunosenescence
inferred← citeshttps://doi.org/10.1007/978-3-319-99375-1_81openalex-snapshot
Age-Specific T Cell Homeostasis
inferred← citeshttps://doi.org/10.1007/978-3-642-12765-6_5openalex-snapshot
Physiologie und Pathophysiologie des Immunsystems
inferred← citeshttps://doi.org/10.1007/978-3-662-54137-1_9openalex-snapshot
Vergessen im Immunsystem: Eine Frage der Passung interagierender Systeme
inferred← citeshttps://doi.org/10.1007/978-981-13-0484-2_9openalex-snapshot
Cellular Determinants of HIV Persistence on Antiretroviral Therapy
inferred← citeshttps://doi.org/10.1007/s00018-010-0362-2openalex-snapshot
The persistence of T cell memory
inferred← citeshttps://doi.org/10.1007/s00018-012-0970-0openalex-snapshot
Immune aging and autoimmunity
inferred← citeshttps://doi.org/10.1007/s00018-021-04122-zopenalex-snapshot
Defects in aminoacyl-tRNA synthetase cause partial B and T cell immunodeficiency
inferred← citeshttps://doi.org/10.1007/s00018-025-05625-9openalex-snapshot
Cell-type-specific requirement for TYK2 in murine immune cells under steady state and challenged conditions
inferred← citeshttps://doi.org/10.1007/s00109-014-1145-2openalex-snapshot
Molecules in medicine mini review: the αβ T cell receptor
inferred← citeshttps://doi.org/10.1007/s00262-010-0936-8openalex-snapshot
IL-21-treated naive CD45RA+ CD8+ T cells represent a reliable source for producing leukemia-reactive cytotoxic T lymphocytes with high proliferative potential and early differentiation phenotype
inferred← citeshttps://doi.org/10.1007/s00262-011-1045-zopenalex-snapshot
Myxoma virus combined with rapamycin treatment enhances adoptive T cell therapy for murine melanoma brain tumors
inferred← citeshttps://doi.org/10.1007/s00262-012-1350-1openalex-snapshot
Mimicking homeostatic proliferation in vitro generates T cells with high anti-tumor function in non-lymphopenic hosts
inferred← citeshttps://doi.org/10.1007/s00262-025-04226-6openalex-snapshot
Empowering exhausted T cells of Glioblastoma patients by Neurotransmitters and Neuropeptides: decreasing immune checkpoint inhibitors, and increasing CD3zeta, proliferation and Glioblastoma arrest
inferred← citeshttps://doi.org/10.1007/s00281-009-0195-yopenalex-snapshot
Lymphoproliferative disorders involving T helper effector cells with defective LAT signalosomes
inferred← citeshttps://doi.org/10.1007/s00393-012-1031-7openalex-snapshot
Stromazellen als Koordinatoren für die adaptive Immunantwort und das immunologische Gedächtnis
inferred← citeshttps://doi.org/10.1007/s00394-018-01891-5openalex-snapshot
Breast milk interleukin-7 and thymic gland development in infancy
inferred← citeshttps://doi.org/10.1007/s00441-014-1889-6openalex-snapshot
Characterization of mouse mediastinal fat-associated lymphoid clusters
inferred← citeshttps://doi.org/10.1007/s10120-018-0841-yopenalex-snapshot
Multi-marker analysis of genomic annotation on gastric cancer GWAS data from Chinese populations
inferred← citeshttps://doi.org/10.1007/s10238-015-0376-zopenalex-snapshot
T cell senescence and cardiovascular diseases
inferred← citeshttps://doi.org/10.1007/s10517-010-0874-7openalex-snapshot
Processes of Homeostatic Proliferation in the Pathogenesis of Autoimmune Glomerulonephritis Induced by Chronic Graft-Versus-Host Reaction
inferred← citeshttps://doi.org/10.1007/s10875-021-01201-5openalex-snapshot
Long-Term Follow-Up of Newborns with 22q11 Deletion Syndrome and Low TRECs
inferred← citeshttps://doi.org/10.1007/s11033-026-11529-zopenalex-snapshot
Exploring the impact of IL-2 cytokine family on skin barrier function: pathophysiology and therapeutic strategies
inferred← citeshttps://doi.org/10.1007/s11357-011-9353-yopenalex-snapshot
Improving immunity in the elderly: current and future lessons from nonhuman primate models
inferred← citeshttps://doi.org/10.1007/s11538-010-9585-5openalex-snapshot
A Theory of Immunodominance and Adaptive Regulation
inferred← citeshttps://doi.org/10.1007/s11538-019-00630-zopenalex-snapshot
A Mathematical Model of the Effects of Aging on Naive T Cell Populations and Diversity
inferred← citeshttps://doi.org/10.1007/s11671-009-9413-8openalex-snapshot
The Influences of Cell Type and ZnO Nanoparticle Size on Immune Cell Cytotoxicity and Cytokine Induction
inferred← citeshttps://doi.org/10.1007/s11892-015-0659-5openalex-snapshot
Targeting Memory T Cells in Type 1 Diabetes
inferred← citeshttps://doi.org/10.1007/s11899-013-0165-2openalex-snapshot
T-Cell Receptor Signaling in Peripheral T-Cell Lymphoma – A Review of Patterns of Alterations in a Central Growth Regulatory Pathway
inferred← citeshttps://doi.org/10.1007/s11904-019-00462-5openalex-snapshot
Tyrosine Kinase Inhibition: a New Perspective in the Fight against HIV
inferred← citeshttps://doi.org/10.1007/s12020-013-9960-8openalex-snapshot
Role of T cells in the modulation of PTH action: physiological and clinical significance
inferred← citeshttps://doi.org/10.1007/s12026-010-8175-9openalex-snapshot
Receptor signaling in immune cell development and function
inferred← citeshttps://doi.org/10.1007/s12026-013-8456-1openalex-snapshot
Understanding the biology of ex vivo-expanded CD8 T cells for adoptive cell therapy: role of CD62L
inferred← citeshttps://doi.org/10.1007/s12026-022-09345-1openalex-snapshot
Soluble factors from TLR4- or TCR-activated cells contribute to stability of the resting phenotype and increase the expression of CXCR4 of human memory CD4 T cells
inferred← citeshttps://doi.org/10.1007/s12185-017-2386-yopenalex-snapshot
Low-dose interleukin-2 as a modulator of Treg homeostasis after HSCT: current understanding and future perspectives
inferred← citeshttps://doi.org/10.1016/b978-0-12-374279-7.10010-4openalex-snapshot
γ c Family Cytokines: Role in Immune Cell Development and Function
inferred← citeshttps://doi.org/10.1016/b978-0-12-397166-1.00014-xopenalex-snapshot
PTH and T-cell Biology
inferred← citeshttps://doi.org/10.1016/b978-0-12-405546-9.00052-2openalex-snapshot
Management of Autoimmunity and Inflammation
inferred← citeshttps://doi.org/10.1016/b978-0-12-415853-5.00046-7openalex-snapshot
Estrogen Deficiency, Postmenopausal Osteoporosis, and Age-Related Bone Loss
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.11232-2openalex-snapshot
Distant Immune and Microbiome Regulation
inferred← citeshttps://doi.org/10.1016/b978-0-12-809633-8.20729-2openalex-snapshot
Invertebrate Adaptive Immunology ☆
inferred← citeshttps://doi.org/10.1016/b978-0-12-813073-5.00032-0openalex-snapshot
Estrogen deficiency and the pathogenesis of osteoporosis
inferred← citeshttps://doi.org/10.1016/b978-0-12-815389-5.00075-7openalex-snapshot
Mechanisms of allograft rejection
inferred← citeshttps://doi.org/10.1016/b978-0-12-818731-9.00038-0openalex-snapshot
Cell-Mediated Immunity
inferred← citeshttps://doi.org/10.1016/b978-0-12-818731-9.00090-2openalex-snapshot
Cytokines in Innate Immunity
inferred← citeshttps://doi.org/10.1016/b978-0-12-824465-4.00180-0openalex-snapshot
Cellular Metabolism Controls Lymphocyte Activation and Differentiation
inferred← citeshttps://doi.org/10.1016/b978-0-128-24465-4.00096-xopenalex-snapshot
γc-Family Cytokines in Health and Disease
inferred← citeshttps://doi.org/10.1016/b978-0-323-56802-9.00028-6openalex-snapshot
Principles and Applications of Cellular Therapy in the Setting of Hematopoietic Cell Transplant
inferred← citeshttps://doi.org/10.1016/b978-0-323-99893-2.00009-9openalex-snapshot
T cell receptors, the molecular bodyguard in αβ T lymphocyte immunity
inferred← citeshttps://doi.org/10.1016/b978-0-443-15283-2.00018-xopenalex-snapshot
Role of cytokines in human immunodeficiency virus (HIV) infection
inferred← citeshttps://doi.org/10.1016/b978-0-443-45128-7.00006-6openalex-snapshot
Cytokine storm (septic shock and COVID-19)
inferred← citeshttps://doi.org/10.1016/b978-0-443-45128-7.00021-2openalex-snapshot
Cytokines with antiviral properties—Interferons
inferred← citeshttps://doi.org/10.1016/b978-0-7234-3691-1.00019-2openalex-snapshot
Aging and the immune system
inferred← citeshttps://doi.org/10.1016/b978-1-4160-6400-8.00004-3openalex-snapshot
Developmental Immunology and Role of Host Defenses in Fetal and Neonatal Susceptibility to Infection
inferred← citeshttps://doi.org/10.1016/b978-2-294-71107-7.50002-0openalex-snapshot
Immunologie générale
inferred← citeshttps://doi.org/10.1016/bs.ircmb.2018.05.007openalex-snapshot
The Single-Cell Phenotypic Identity of Human CD8+ and CD4+ T Cells
inferred← citeshttps://doi.org/10.1016/j.addr.2009.11.011openalex-snapshot
Application of nanotechnologies for improved immune response against infectious diseases in the developing world
inferred← citeshttps://doi.org/10.1016/j.addr.2013.12.011openalex-snapshot
Human immunity in vitro — Solving immunogenicity and more
inferred← citeshttps://doi.org/10.1016/j.addr.2014.01.002openalex-snapshot
Pharmacokinetic/pharmacodynamic modelling approaches in paediatric infectious diseases and immunology
inferred← citeshttps://doi.org/10.1016/j.ajhg.2023.11.013openalex-snapshot
Interaction molecular QTL mapping discovers cellular and environmental modifiers of genetic regulatory effects
inferred← citeshttps://doi.org/10.1016/j.ajpath.2020.03.016openalex-snapshot
Aged Mice Exhibit Severe Exacerbations of Dry Eye Disease with an Amplified Memory Th17 Cell Response
inferred← citeshttps://doi.org/10.1016/j.alit.2017.03.005openalex-snapshot
Maintenance of pathogenic Th2 cells in allergic disorders
inferred← citeshttps://doi.org/10.1016/j.anai.2015.01.013openalex-snapshot
Interleukin-25 and mucosal T cells in noneosinophilic and eosinophilic chronic rhinosinusitis
inferred← citeshttps://doi.org/10.1016/j.archger.2024.105376openalex-snapshot
Changes in immune cell subtypes during ageing
inferred← citeshttps://doi.org/10.1016/j.archger.2024.105560openalex-snapshot
Association between immune cells, inflammatory cytokines, and sarcopenia: Insights from a Mendelian randomization analysis
inferred← citeshttps://doi.org/10.1016/j.arr.2010.08.003openalex-snapshot
Persistent viral infections and immune aging
inferred← citeshttps://doi.org/10.1016/j.arr.2010.09.006openalex-snapshot
Expansions of NK-like αβT cells with chronologic aging: Novel lymphocyte effectors that compensate for functional deficits of conventional NK cells and T cells
inferred← citeshttps://doi.org/10.1016/j.bbadis.2018.04.010openalex-snapshot
Anti-IL-7 receptor-α treatment ameliorates newly established Sjögren's-like exocrinopathy in non-obese diabetic mice
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2014.09.001openalex-snapshot
Linking form to function: Biophysical aspects of artificial antigen presenting cell design
inferred← citeshttps://doi.org/10.1016/j.bbih.2024.100764openalex-snapshot
Higher T central and lower effector memory cells in bipolar disorder: A differentiation abnormality?
inferred← citeshttps://doi.org/10.1016/j.bbmt.2012.07.009openalex-snapshot
Allospecific CD4+ Effector Memory T Cells Do Not Induce Graft-versus-Host Disease in Mice
inferred← citeshttps://doi.org/10.1016/j.bbmt.2014.11.010openalex-snapshot
CD19+CD21low B Cells and CD4+CD45RA+CD31+ T Cells Correlate with First Diagnosis of Chronic Graft-versus-Host Disease
inferred← citeshttps://doi.org/10.1016/j.bbrc.2012.07.065openalex-snapshot
ZFAT plays critical roles in peripheral T cell homeostasis and its T cell receptor-mediated response
inferred← citeshttps://doi.org/10.1016/j.bbrc.2020.10.079openalex-snapshot
T-cell dysregulation in COVID-19
inferred← citeshttps://doi.org/10.1016/j.bbrep.2016.06.006openalex-snapshot
T cell up-regulation of CD127 is associated with reductions in the homeostatic set point of the peripheral T cell pool during malnourishment
inferred← citeshttps://doi.org/10.1016/j.bj.2022.03.008openalex-snapshot
Negative times negative equals positive, THEMIS sets the rule on thymic selection and peripheral T cell responses
inferred← citeshttps://doi.org/10.1016/j.bone.2017.04.009openalex-snapshot
Osteomicrobiology: The influence of gut microbiota on bone in health and disease
inferred← citeshttps://doi.org/10.1016/j.canlet.2024.216714openalex-snapshot
From lymphopenia to restoration: IL-7 immunotherapy for lymphocyte recovery in glioblastoma
inferred← citeshttps://doi.org/10.1016/j.cell.2014.10.026openalex-snapshot
Spatial Map of Human T Cell Compartmentalization and Maintenance over Decades of Life
inferred← citeshttps://doi.org/10.1016/j.cell.2019.07.049openalex-snapshot
The Bone Marrow Protects and Optimizes Immunological Memory during Dietary Restriction
inferred← citeshttps://doi.org/10.1016/j.cellimm.2011.03.006openalex-snapshot
γ Chain transducing element: A shared pathway between endocrine and immune system
inferred← citeshttps://doi.org/10.1016/j.cellimm.2012.02.005openalex-snapshot
Homeostatic signals do not drive post-thymic T cell maturation
inferred← citeshttps://doi.org/10.1016/j.cellimm.2013.04.010openalex-snapshot
Irinotecan combined with co-stimulatory molecule blockade prolongs survival of cardiac allografts in alloantigen-primed mice
inferred← citeshttps://doi.org/10.1016/j.cellimm.2023.104795openalex-snapshot
Development of a highly cytotoxic, clinical-grade virus-specific T cell product for adoptive T cell therapy
inferred← citeshttps://doi.org/10.1016/j.celrep.2014.09.004openalex-snapshot
An MHC II-Dependent Activation Loop between Adipose Tissue Macrophages and CD4+ T Cells Controls Obesity-Induced Inflammation
inferred← citeshttps://doi.org/10.1016/j.celrep.2015.07.008openalex-snapshot
Metabolic Damage and Premature Thymus Aging Caused by Stromal Catalase Deficiency
inferred← citeshttps://doi.org/10.1016/j.celrep.2017.08.065openalex-snapshot
miR-150-Mediated Foxo1 Regulation Programs CD8+ T Cell Differentiation
inferred← citeshttps://doi.org/10.1016/j.celrep.2019.03.004openalex-snapshot
Lymphocyte Activation Gene-3 Maintains Mitochondrial and Metabolic Quiescence in Naive CD4+ T Cells
inferred← citeshttps://doi.org/10.1016/j.celrep.2019.11.056openalex-snapshot
Tissue-Resident Memory T Cells Mediate Immune Homeostasis in the Human Pancreas Through the PD-1/PD-L1 Pathway
inferred← citeshttps://doi.org/10.1016/j.celrep.2020.107910openalex-snapshot
Cell Competition, the Kinetics of Thymopoiesis, and Thymus Cellularity Are Regulated by Double-Negative 2 to 3 Early Thymocytes
inferred← citeshttps://doi.org/10.1016/j.celrep.2021.109981openalex-snapshot
The cell-surface 5′-nucleotidase CD73 defines a functional T memory cell subset that declines with age
inferred← citeshttps://doi.org/10.1016/j.celrep.2021.110219openalex-snapshot
In vivo availability of the cytokine IL-7 constrains the survival and homeostasis of peripheral iNKT cells
inferred← citeshttps://doi.org/10.1016/j.celrep.2023.112195openalex-snapshot
TRIB2 safeguards naive T cell homeostasis during aging
inferred← citeshttps://doi.org/10.1016/j.celrep.2023.112302openalex-snapshot
DNA-damaged podocyte-CD8 T cell crosstalk exacerbates kidney injury by altering DNA methylation
inferred← citeshttps://doi.org/10.1016/j.celrep.2026.116980openalex-snapshot
Heterogeneity and plasticity of the naive CD4+ T cell compartment
inferred← citeshttps://doi.org/10.1016/j.celrep.2026.117745openalex-snapshot
Circulating memory-phenotype CD4+ T cells rapidly accumulate in the ischemic gut to exacerbate tissue injury in an innate manner
inferred← citeshttps://doi.org/10.1016/j.clicom.2025.09.003openalex-snapshot
Reprogramming immunity: Emerging therapeutic frontiers and clinical trial advances of CAR-T cell therapy in autoimmune diseases
inferred← citeshttps://doi.org/10.1016/j.clim.2010.04.011openalex-snapshot
Secondary immunologic consequences in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)
inferred← citeshttps://doi.org/10.1016/j.clim.2010.06.004openalex-snapshot
Analyses of T cell phenotype and function reveal an altered T cell homeostasis in systemic sclerosis
inferred← citeshttps://doi.org/10.1016/j.clim.2015.08.007openalex-snapshot
Interleukin-7 is required for CD4 + T cell activation and autoimmune neuroinflammation
inferred← citeshttps://doi.org/10.1016/j.clim.2021.108685openalex-snapshot
T cell markers recount the course of immunosenescence in healthy individuals and chronic kidney disease
inferred← citeshttps://doi.org/10.1016/j.clim.2023.109733openalex-snapshot
High Epstein-Barr virus capsid antigen IgG level associates with the carriership of CD8+ T cell somatic mutations in the STAT3 SH2 domain
inferred← citeshttps://doi.org/10.1016/j.cmet.2022.02.003openalex-snapshot
Metabolic programs tailor T cell immunity in viral infection, cancer, and aging
inferred← citeshttps://doi.org/10.1016/j.coi.2014.12.005openalex-snapshot
Determinants of immunodominance for CD4 T cells
inferred← citeshttps://doi.org/10.1016/j.coph.2009.04.008openalex-snapshot
Anti-inflammatory and pro-inflammatory roles of TGF-β, IL-10, and IL-22 in immunity and autoimmunity
inferred← citeshttps://doi.org/10.1016/j.critrevonc.2015.10.005openalex-snapshot
Adoptive transfer of Aspergillus-specific T cells as a novel anti-fungal therapy for hematopoietic stem cell transplant recipients: Progress and challenges
inferred← citeshttps://doi.org/10.1016/j.critrevonc.2025.104635openalex-snapshot
Clinical benefit of immune checkpoint inhibitors in elderly cancer patients: Current evidence from immunosenescence pathophysiology to clinical trial results
inferred← citeshttps://doi.org/10.1016/j.cyto.2016.02.006openalex-snapshot
Cytokines and persistent viral infections
inferred← citeshttps://doi.org/10.1016/j.cyto.2017.07.019openalex-snapshot
A new approach to the role of IL-7 and TGF-ß in the in vitro generation of thymus-derived CD4+CD25+Foxp3+ regulatory T cells
inferred← citeshttps://doi.org/10.1016/j.cyto.2021.155547openalex-snapshot
Descriptive modification of inflammatory markers in HIV patients after cART initiation according to gender, smoking habit, CMV infection, BMI and serum lipids
inferred← citeshttps://doi.org/10.1016/j.cyto.2022.156049openalex-snapshot
IL-7: Comprehensive review
inferred← citeshttps://doi.org/10.1016/j.cyto.2025.156973openalex-snapshot
Interleukin-enhanced CAR-engineered immune cells in tumor immunotherapy: current insights and future perspectives
inferred← citeshttps://doi.org/10.1016/j.cytogfr.2010.05.002openalex-snapshot
Regulation of immune cell homeostasis by type I interferons
inferred← citeshttps://doi.org/10.1016/j.cytogfr.2012.05.001openalex-snapshot
The role of cytokines in the establishment, persistence and eradication of the HIV reservoir
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