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Naive T cells proliferate strongly in neonatal mice in response to self-peptide/self-MHC complexes

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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/(sici)1521-4141(199902)29:02<608::aid-immu608>3.0.co;2-aopenalex-snapshot

Naïve cytotoxic T lymphocytes spontaneously acquire effector function in lymphocytopenic recipients: A pitfall for T cell memory studies?

inferredcites →https://doi.org/10.1002/1521-4141(200003)30:3<738::aid-immu738>3.0.co;2-yopenalex-snapshot

Regulation and kinetics of premigrant thymocyte expansion

inferredcites →https://doi.org/10.1002/1521-4141(200108)31:8<2256::aid-immu2256>3.0.co;2-8openalex-snapshot

Naive CD4+ lymphocytes convert to anergic or memory-like cells in T cell-deprived recipients

inferredcites →https://doi.org/10.1002/eji.1830220207openalex-snapshot

Seeding of neonatal lymph nodes by T cells and identification of a novel population of CD3 − CD4 + cells

inferredcites →https://doi.org/10.1002/eji.1830240533openalex-snapshot

Differential contribution of thymic outputs and peripheral expansion in the development of peripheral T cell pools

inferredcites →https://doi.org/10.1002/eji.1830250802openalex-snapshot

The peripheral T cell repertoire: independent homeostatic regulation of virgin and activated CD8+ T cell pools

inferredcites →https://doi.org/10.1002/eji.1830261251openalex-snapshot

Cell division in the compartment of naive and memory T lymphocytes

inferredcites →https://doi.org/10.1002/j.1460-2075.1995.tb00146.xopenalex-snapshot

Altered T cell development in mice with a targeted mutation of the CD3‐epsilon gene.

inferredcites →https://doi.org/10.1006/jaut.1996.0026openalex-snapshot

T Cell-Mediated Maintenance of Natural Self-Tolerance: its Breakdown as a Possible Cause of Various Autoimmune Diseases

inferredcites →https://doi.org/10.1006/smim.1997.0090openalex-snapshot

Lymphocyte homeostasis

inferredcites →https://doi.org/10.1016/0092-8674(91)90448-8openalex-snapshot

Mice lacking MHC class II molecules

inferredcites →https://doi.org/10.1016/0092-8674(93)90225-fopenalex-snapshot

Another view of the selective model of thymocyte selection

inferredcites →https://doi.org/10.1016/1074-7613(95)90180-9openalex-snapshot

Interleukin-2 receptor α chain regulates the size and content of the peripheral lymphoid compartment

inferredcites →https://doi.org/10.1016/s0167-5699(98)01344-9openalex-snapshot

The organization of mature T-cell pools

inferredcites →https://doi.org/10.1016/s0167-5699(99)01473-5openalex-snapshot

T-cell function in newborn mice and humans

inferredcites →https://doi.org/10.1016/s0167-5699(99)01548-0openalex-snapshot

Neonatal immunity: how well has it grown up?

inferredcites →https://doi.org/10.1016/s0198-8859(97)00202-4openalex-snapshot

Analysis of Neonatal T Cell and Antigen Presenting Cell Functions

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)80515-4openalex-snapshot

Targeted Complementation of MHC Class II Deficiency by Intrathymic Delivery of Recombinant Adenoviruses

inferredcites →https://doi.org/10.1038/333742a0openalex-snapshot

Tolerance in T-cell-receptor transgenic mice involves deletion of nonmature CD4+8+ thymocytes

inferredcites →https://doi.org/10.1038/341746a0openalex-snapshot

Selective development of CD4+ T cells in transgenic mice expressing a class II MHC-restricted antigen receptor

inferredcites →https://doi.org/10.1038/342559a0openalex-snapshot

Tolerance induction in double specific T-cell receptor transgenic mice varies with antigen

inferredcites →https://doi.org/10.1038/35005508openalex-snapshot

Selecting and maintaining a diverse T-cell repertoire

inferredcites →https://doi.org/10.1038/352621a0openalex-snapshot

Development and function of T cells in mice rendered interleukin-2 deficient by gene targeting

inferredcites →https://doi.org/10.1038/46218openalex-snapshot

Selecting and maintaining a diverse T-cell repertoire

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/10.1073/pnas.161126098openalex-snapshot

IL-7 is critical for homeostatic proliferation and survival of naïve T cells

inferredcites →https://doi.org/10.1073/pnas.96.23.13306openalex-snapshot

Homeostatic expansion and phenotypic conversion of naïve T cells in response to self peptide/MHC ligands

inferredcites →https://doi.org/10.1084/jem.125.5.947openalex-snapshot

POSTTHYMECTOMY WASTING ASSOCIATED WITH AUTOIMMUNE PHENOMENA

inferredcites →https://doi.org/10.1084/jem.156.6.1565openalex-snapshot

Study on cellular events in postthymectomy autoimmune oophoritis in mice. I. Requirement of Lyt-1 effector cells for oocytes damage after adoptive transfer.

inferredcites →https://doi.org/10.1084/jem.156.6.1577openalex-snapshot

Study on cellular events in post-thymectomy autoimmune oophoritis in mice. II. Requirement of Lyt-1 cells in normal female mice for the prevention of oophoritis.

inferredcites →https://doi.org/10.1084/jem.177.4.891openalex-snapshot

The life span of naive alpha/beta T cells in secondary lymphoid organs.

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.184.2.387openalex-snapshot

Autoimmune disease as a consequence of developmental abnormality of a T cell subpopulation.

inferredcites →https://doi.org/10.1084/jem.186.7.1099openalex-snapshot

Peripheral Selection of T Cell Repertoires: The Role of Continuous Thymus Output

inferredcites →https://doi.org/10.1084/jem.186.8.1223openalex-snapshot

Survival of Mature CD4 T Lymphocytes Is Dependent on Major Histocompatibility Complex Class II–expressing Dendritic Cells

inferredcites →https://doi.org/10.1084/jem.186.8.1269openalex-snapshot

Peripheral T Cell Survival Requires Continual Ligation of the T Cell Receptor to Major Histocompatibility Complex–Encoded Molecules

inferredcites →https://doi.org/10.1084/jem.190.1.53openalex-snapshot

Anergy and Cytokine-Mediated Suppression as Distinct Superantigen-Induced Tolerance Mechanisms in Vivo

inferredcites →https://doi.org/10.1084/jem.190.3.367openalex-snapshot

Cd4+ T Cell Division in Irradiated Mice Requires Peptides Distinct from Those Responsible for Thymic Selection

inferredcites →https://doi.org/10.1084/jem.192.4.549openalex-snapshot

Homeostasis-Stimulated Proliferation Drives Naive T Cells to Differentiate Directly into Memory T Cells

inferredcites →https://doi.org/10.1084/jem.192.4.557openalex-snapshot

Naive T Cells Transiently Acquire a Memory-like Phenotype during Homeostasis-Driven Proliferation

inferredcites →https://doi.org/10.1084/jem.192.4.f9openalex-snapshot

Homeostatic T Cell Proliferation

inferredcites →https://doi.org/10.1093/intimm/10.4.371openalex-snapshot

Regulatory CD4 T cells: expression of IL-2R alpha chain, resistance to clonal deletion and IL-2 dependency

inferredcites →https://doi.org/10.1093/intimm/2.5.419openalex-snapshot

Analysis of recent thymic emigrants with subse- and maturity-related markers

inferredcites →https://doi.org/10.1093/intimm/7.12.1897openalex-snapshot

Neonatal impaired response to viral superantigen encoded by MMTV(SW) and Mtv-7

inferredcites →https://doi.org/10.1126/science.2112266openalex-snapshot

Normal Development of Mice Deficient in β 2 M, MCClass I Proteins, and CD8 + T Cells

inferredcites →https://doi.org/10.1126/science.271.5256.1723openalex-snapshot

Neonatal Tolerance Revisited: Turning on Newborn T Cells with Dendritic Cells

inferredcites →https://doi.org/10.1126/science.271.5256.1726openalex-snapshot

Induction of Protective CTL Responses in Newborn Mice by a Murine Retrovirus

inferredcites →https://doi.org/10.1126/science.271.5256.1728openalex-snapshot

Induction of T H 1 and T H 2 Immunity in Neonatal Mice

inferredcites →https://doi.org/10.1126/science.274.5293.1726openalex-snapshot

Photolysis of the Carbon Monoxide Complex of Myoglobin: Nanosecond Time-Resolved Crystallography

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.290.5489.127openalex-snapshot

Long-Term Survival But Impaired Homeostatic Proliferation of Naïve T Cells in the Absence of p56 lck

inferredcites →https://doi.org/10.1126/science.8073282openalex-snapshot

Lymphocyte life-span and memory

inferredcites →https://doi.org/10.1385/ir:22:2-3:177openalex-snapshot

T Cell Immunity in Neonates

inferredcites →https://doi.org/10.4049/jimmunol.132.1.25openalex-snapshot

The functional capabilities of cells leaving the thymus.

inferredcites →https://doi.org/10.4049/jimmunol.159.10.4848openalex-snapshot

Expansion of mature thymocyte subsets before emigration to the periphery

inferredcites →https://doi.org/10.4049/jimmunol.162.9.5164openalex-snapshot

Distribution of Cycling T Lymphocytes in Blood and Lymphoid Organs During Immune Responses

inferredcites →https://doi.org/10.4049/jimmunol.165.4.1733openalex-snapshot

Cutting Edge: Naive T Cells Masquerading as Memory Cells

inferredcites →https://doi.org/10.4049/jimmunol.165.7.3689openalex-snapshot

Differential Survival of Naive CD4 and CD8 T Cells

inferredcites →https://doi.org/10.4049/jimmunol.166.9.5515openalex-snapshot

IL-12 Enhances CD8 T Cell Homeostatic Expansion

inferredcites →https://doi.org/10.4049/jimmunol.167.4.2030openalex-snapshot

Adaptive Tolerance of CD4+ T Cells In Vivo: Multiple Thresholds in Response to a Constant Level of Antigen Presentation

What points at this work

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

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Priming and Maturation of the Human Fetal Mucosal Immunity Occurs Early in Fetal Development

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Future Strategies in Immunotherapy

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Improving thymus implantation for congenital athymia with interleukin‐7

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Frequent expression of the natural killer cell receptor KLRG1 in human cord blood T cells: correlation with replicative history

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Gut flora antigens are not important in the maintenance of regulatory T cell heterogeneity and homeostasis

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Innate and virtual memory T cells in man

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CXCR3high CD8+ T cells with naïve phenotype and high capacity for IFN‐γ production are generated during homeostatic T‐cell proliferation

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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/10.1007/978-1-0716-0266-9_21openalex-snapshot

Studying Peripheral T Cell Homeostasis in Mice: A Concise Technical Review

inferred← citeshttps://doi.org/10.1007/978-1-4020-9063-9_16openalex-snapshot

CD8 Clonal Expansions in Mice: An Age-associated Alteration of CD8 Memory T-cells

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Thy(–im)munosenescence: The Ageing of the Thymus and Its Impact on the Immune System

inferred← citeshttps://doi.org/10.1007/s00281-017-0648-7openalex-snapshot

Tissue compartmentalization of T cell responses during early life

inferred← citeshttps://doi.org/10.1007/s00281-017-0650-0openalex-snapshot

In utero development of memory T cells

inferred← citeshttps://doi.org/10.1007/s12026-015-8725-2openalex-snapshot

Mechanisms of diabetic autoimmunity: II—Is diabetes a central or peripheral disorder of effector and regulatory cells?

inferred← citeshttps://doi.org/10.1007/s12026-015-8753-yopenalex-snapshot

Mechanisms of diabetic autoimmunity: I—the inductive interface between islets and the immune system at onset of inflammation

inferred← citeshttps://doi.org/10.1016/b978-0-12-374279-7.19011-3openalex-snapshot

Neonatal Immunity

inferred← citeshttps://doi.org/10.1016/b978-0-128-24465-4.00517-2openalex-snapshot

Neonatal Immunity

inferred← citeshttps://doi.org/10.1016/bs.ai.2014.12.001openalex-snapshot

Innate Memory T cells

inferred← citeshttps://doi.org/10.1016/j.celrep.2025.115903openalex-snapshot

Gene-regulatory programs that specify age-related differences during thymocyte development

inferred← citeshttps://doi.org/10.1016/j.coi.2004.09.003openalex-snapshot

Homeostasis and T cell regulation

inferred← citeshttps://doi.org/10.1016/j.coi.2017.12.005openalex-snapshot

The influence of developmental timing on B cell diversity

inferred← citeshttps://doi.org/10.1016/j.cyto.2009.09.008openalex-snapshot

Regulation of memory T cells by γc cytokines

inferred← citeshttps://doi.org/10.1016/j.cyto.2016.01.003openalex-snapshot

Homeostatic cytokines in immune reconstitution and graft-versus-host disease

inferred← citeshttps://doi.org/10.1016/j.devcel.2019.09.008openalex-snapshot

Maturation of the Human Intestinal Immune System Occurs Early in Fetal Development

inferred← citeshttps://doi.org/10.1016/j.exphem.2006.10.010openalex-snapshot

Lymphopenia-induced proliferation of donor T cells reduces their capacity for causing acute graft-versus-host disease

inferred← citeshttps://doi.org/10.1016/j.imlet.2006.08.001openalex-snapshot

T cell homeostasis in steady state and lymphopenic conditions

inferred← citeshttps://doi.org/10.1016/j.immuni.2006.12.002openalex-snapshot

The Lymphopenic Mouse in Immunology: From Patron to Pariah

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A Central Role for mTOR Kinase in Homeostatic Proliferation Induced CD8+ T Cell Memory and Tumor Immunity

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Plasticity of Foxp3+ T Cells Reflects Promiscuous Foxp3 Expression in Conventional T Cells but Not Reprogramming of Regulatory T Cells

inferred← citeshttps://doi.org/10.1016/j.isci.2024.109775openalex-snapshot

Human CD4+ memory phenotype T cells use mitochondrial metabolism to generate sensitive IFN-γ responses

inferred← citeshttps://doi.org/10.1016/j.it.2005.06.002openalex-snapshot

Control of peripheral T-lymphocyte tolerance in neonates and adults

inferred← citeshttps://doi.org/10.1016/j.jaut.2011.02.009openalex-snapshot

Programmed death-1 is required for systemic self-tolerance in newly generated T cells during the establishment of immune homeostasis

inferred← citeshttps://doi.org/10.1016/j.jaut.2017.05.003openalex-snapshot

The molecular signature of murine T cell homeostatic proliferation reveals both inflammatory and immune inhibition patterns

inferred← citeshttps://doi.org/10.1016/j.molimm.2008.03.009openalex-snapshot

TCR repertoire dynamics in the pancreatic lymph nodes of non-obese diabetic (NOD) mice at the time of disease initiation

inferred← citeshttps://doi.org/10.1016/j.placenta.2025.05.011openalex-snapshot

Reframing the paradigm-rethinking placental and fetal immunity

inferred← citeshttps://doi.org/10.1016/j.smim.2005.02.003openalex-snapshot

T cell homeostasis: Keeping useful T cells alive and live T cells useful

inferred← citeshttps://doi.org/10.1016/j.smim.2005.02.005openalex-snapshot

Endogenous proliferation: Burst-like CD4 T cell proliferation in lymphopenic settings

inferred← citeshttps://doi.org/10.1016/j.smim.2009.02.006openalex-snapshot

CD4 memory T cells: What are they and what can they do?

inferred← citeshttps://doi.org/10.1016/j.smim.2012.04.010openalex-snapshot

IL-7 signaling and CD127 receptor regulation in the control of T cell homeostasis

inferred← citeshttps://doi.org/10.1016/j.vaccine.2009.09.091openalex-snapshot

Neonatal immunization with Listeria monocytogenes induces T cells with an adult-like avidity, sensitivity, and TCR-Vβ repertoire, and does not adversely impact the response to boosting

inferred← citeshttps://doi.org/10.1016/s1074-7613(02)00508-3openalex-snapshot

Neonates Support Lymphopenia-Induced Proliferation

inferred← citeshttps://doi.org/10.1038/icb.2008.12openalex-snapshot

T cell homeostasis

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Role for Bcl-6 in the generation and maintenance of memory CD8+ T cells

inferred← citeshttps://doi.org/10.1038/nri.2017.34openalex-snapshot

Antigen-inexperienced memory CD8+ T cells: where they come from and why we need them

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Foreign antigen-independent memory-phenotype CD4+ T cells: a new player in innate immunity?

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Neonatal adaptive immunity comes of age

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Maintaining the norm: T-cell homeostasis

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Building a T cell compartment: how immune cell development shapes function

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Diversity of the Immune Repertoire and Immunoregulation

inferred← citeshttps://doi.org/10.1073/pnas.0307339101openalex-snapshot

Competition for self-peptide-MHC complexes and cytokines between naïve and memory CD8 + T cells expressing the same or different T cell receptors

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Spontaneous proliferation, a response of naïve CD4 T cells determined by the diversity of the memory cell repertoire

inferred← citeshttps://doi.org/10.1073/pnas.0604183103openalex-snapshot

Role of T and NK cells and IL7/IL7r interactions during neonatal maturation of lymph nodes

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Hyper innate responses in neonates lead to increased morbidity and mortality after infection

inferred← citeshttps://doi.org/10.1073/pnas.0806487105openalex-snapshot

The nature of the lymphopenic environment dictates protective function of homeostatic-memory CD8 + T cells

inferred← citeshttps://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

inferred← citeshttps://doi.org/10.1073/pnas.1307572110openalex-snapshot

Virtual memory CD8 T cells display unique functional properties

inferred← citeshttps://doi.org/10.1073/pnas.1818327116openalex-snapshot

Regulatory T cells limit unconventional memory to preserve the capacity to mount protective CD8 memory responses to pathogens

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Influence of first-wave derived T lymphocytes in the long term functional reconstitution of allogeneic T cell deficient hosts

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Extrathymic T cells expand in nude mice following different allogeneic stimuli

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Essential Role of Survivin, an Inhibitor of Apoptosis Protein, in T Cell Development, Maturation, and Homeostasis

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Antigen-specific peripheral shaping of the natural regulatory T cell population

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The antigen-specific CD8+ T cell repertoire in unimmunized mice includes memory phenotype cells bearing markers of homeostatic expansion

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Reduced generation of lung tissue–resident memory T cells during infancy

inferred← citeshttps://doi.org/10.1093/infdis/jiz531openalex-snapshot

Immune predictors of mortality following RNA virus infection

inferred← citeshttps://doi.org/10.1093/intimm/dxh360openalex-snapshot

Neonate-primed CD8+ memory cells rival adult-primed memory cells in antigen-driven expansion and anti-viral protection

inferred← citeshttps://doi.org/10.1093/intimm/dxl009openalex-snapshot

Activation of thymic T cells by MHC alloantigen requires syngeneic, activated CD4+ T cells and B cells as APC

inferred← citeshttps://doi.org/10.1097/01.cji.0000165356.03924.e7openalex-snapshot

Cytokine Signals in T-Cell Homeostasis

inferred← citeshttps://doi.org/10.1111/imr.13185openalex-snapshot

Shaping immunity for life: Layered development of CD8 + T cells

inferred← citeshttps://doi.org/10.1111/j.1365-2567.2004.01831.xopenalex-snapshot

The concept of space and competition in immune regulation

inferred← citeshttps://doi.org/10.1111/j.1365-2567.2008.02855.xopenalex-snapshot

Susceptibility of neonatal T cells and adult thymocytes to peripheral tolerance to allogeneic stimuli

inferred← citeshttps://doi.org/10.1111/j.1432-2277.2006.00350.xopenalex-snapshot

CD52 ligation induces CD4 and CD8 down modulation in vivo and in vitro

inferred← citeshttps://doi.org/10.1111/j.1600-6143.2012.04008.xopenalex-snapshot

Lymphodepletion and Homeostatic Proliferation: Implications for Transplantation

inferred← citeshttps://doi.org/10.1111/joa.12546openalex-snapshot

Survival of motor neurone protein is required for normal postnatal development of the spleen

inferred← citeshttps://doi.org/10.1111/pai.13583openalex-snapshot

A role for metabolism in determining neonatal immune function

inferred← citeshttps://doi.org/10.1126/sciadv.adx8037openalex-snapshot

Neonatal regulatory T cells persist into adulthood across multiple tissues with high enrichment in the skin

inferred← citeshttps://doi.org/10.1128/jvi.77.14.7872-7879.2003openalex-snapshot

Increased Thymic Output during Acute Measles Virus Infection

inferred← citeshttps://doi.org/10.1128/jvi.80.10.4949-4961.2006openalex-snapshot

Mice Develop Effective but Delayed Protective Immune Responses When Immunized as Neonates either Intranasally with Nonliving VP6/LT(R192G) or Orally with Live Rhesus Rotavirus Vaccine Candidates

inferred← citeshttps://doi.org/10.1142/s0218339011003919openalex-snapshot

SUFFICIENT TO RECOGNIZE SELF TO ATTACK NON-SELF: BLUEPRINT FOR A ONE-SIGNAL T CELL MODEL

inferred← citeshttps://doi.org/10.1146/annurev-immunol-082223-041615openalex-snapshot

T Cell Development and Responses in Human Immune System Mice

inferred← citeshttps://doi.org/10.1172/jci17865openalex-snapshot

IL-7 enhances peripheral T cell reconstitution after allogeneic hematopoietic stem cell transplantation

inferred← citeshttps://doi.org/10.1182/blood-2004-03-0805openalex-snapshot

Establishment of the CD4+ T-cell pool in healthy children and untreated children infected with HIV-1

inferred← citeshttps://doi.org/10.1182/blood-2006-01-0017openalex-snapshot

Self-recognition is crucial for maintaining the peripheral CD4+ T-cell pool in a nonlymphopenic environment

inferred← citeshttps://doi.org/10.1182/blood-2008-02-139154openalex-snapshot

Life after the thymus: CD31+ and CD31− human naive CD4+ T-cell subsets

inferred← citeshttps://doi.org/10.1182/blood-2008-08-173658openalex-snapshot

Murine neonatal recent thymic emigrants are phenotypically and functionally distinct from adult recent thymic emigrants

inferred← citeshttps://doi.org/10.1186/s12979-026-00582-8openalex-snapshot

Virtual memory CD8⁺ T cells in aging: heterogeneity, bystander protection, inflammatory potential, and inhibitory regulation

inferred← citeshttps://doi.org/10.1189/jlb.0105050openalex-snapshot

T cell homeostasis in tolerance and immunity

inferred← citeshttps://doi.org/10.1371/journal.pone.0024226openalex-snapshot

Helios Expression Is a Marker of T Cell Activation and Proliferation

inferred← citeshttps://doi.org/10.1371/journal.ppat.1003572openalex-snapshot

Acute Neonatal Infections ‘Lock-In’ a Suboptimal CD8+ T Cell Repertoire with Impaired Recall Responses

inferred← citeshttps://doi.org/10.1371/journal.ppat.1009287openalex-snapshot

Baseline T cell immune phenotypes predict virologic and disease control upon SARS-CoV infection in Collaborative Cross mice

inferred← citeshttps://doi.org/10.1534/genetics.115.179176openalex-snapshot

MicroRNAs and Their Targets Are Differentially Regulated in Adult and Neonatal Mouse CD8+ T Cells

inferred← citeshttps://doi.org/10.2139/ssrn.4883498openalex-snapshot

Atlas of the Immune System Development in the Fetal Blood

inferred← citeshttps://doi.org/10.2174/157339507781483496openalex-snapshot

Heterogeneity in the CD4 T Cell Compartment and the Variability of Neonatal Immune Responsiveness

inferred← citeshttps://doi.org/10.3389/fendo.2021.582614openalex-snapshot

Sex Differences in the Immune System Become Evident in the Perinatal Period in the Four Core Genotypes Mouse

inferred← citeshttps://doi.org/10.3389/fimmu.2018.00547openalex-snapshot

Spontaneous T Cell Proliferation: A Physiologic Process to Create and Maintain Homeostatic Balance and Diversity of the Immune System

inferred← citeshttps://doi.org/10.3389/fimmu.2024.1293892openalex-snapshot

Regulatory CD4+ T cells: permanent or temporary suppressors of immunity

inferred← citeshttps://doi.org/10.3389/fped.2016.00141openalex-snapshot

Rapid CD8+ Function Is Critical for Protection of Neonatal Mice from an Extracellular Bacterial Enteropathogen

inferred← citeshttps://doi.org/10.3390/ijms22084152openalex-snapshot

Lymphopenia, Lymphopenia-Induced Proliferation, and Autoimmunity

inferred← citeshttps://doi.org/10.3390/vaccines8030546openalex-snapshot

The Power of First Impressions: Can Influenza Imprinting during Infancy Inform Vaccine Design?

inferred← citeshttps://doi.org/10.4049/jimmunol.0901954openalex-snapshot

Autoimmunity during Thymectomy-Induced Lymphopenia: Role of Thymus Ablation and Initial Effector T Cell Activation Timing in Nonobese Diabetic Mice

inferred← citeshttps://doi.org/10.4049/jimmunol.1100394openalex-snapshot

Human Natural Regulatory T Cell Development, Suppressive Function, and Postthymic Maturation in a Humanized Mouse Model

inferred← citeshttps://doi.org/10.4049/jimmunol.1102213openalex-snapshot

Derivation and Maintenance of Virtual Memory CD8 T Cells

inferred← citeshttps://doi.org/10.4049/jimmunol.1103152openalex-snapshot

IL-2 and IL-7 Determine the Homeostatic Balance between the Regulatory and Conventional CD4+ T Cell Compartments during Peripheral T Cell Reconstitution

inferred← citeshttps://doi.org/10.4049/jimmunol.1203149openalex-snapshot

CD8α+ Dendritic Cell Trans Presentation of IL-15 to Naive CD8+ T Cells Produces Antigen-Inexperienced T Cells in the Periphery with Memory Phenotype and Function

inferred← citeshttps://doi.org/10.4049/jimmunol.1400553openalex-snapshot

Rapid Proliferation and Differentiation Impairs the Development of Memory CD8+ T Cells in Early Life

inferred← citeshttps://doi.org/10.4049/jimmunol.1501643openalex-snapshot

Cutting Edge: Innate Lymphoid Cells Suppress Homeostatic T Cell Expansion in Neonatal Mice

inferred← citeshttps://doi.org/10.4049/jimmunol.170.11.5414openalex-snapshot

Memory Phenotype of CD8+ T Cells in MHC Class Ia-Deficient Mice

inferred← citeshttps://doi.org/10.4049/jimmunol.170.2.672openalex-snapshot

Cutting Edge: Homeostatic Proliferation of Peripheral T Lymphocytes Is Regulated by Clonal Competition

inferred← citeshttps://doi.org/10.4049/jimmunol.170.4.1667openalex-snapshot

CD40 Ligand in Pathogenesis of Autoimmune Ovarian Disease of Day 3-Thymectomized Mice: Implication for CD40 Ligand Antibody Therapy

inferred← citeshttps://doi.org/10.4049/jimmunol.170.9.4548openalex-snapshot

Murine Neonatal Lymphocytes Show Rapid Early Cell Cycle Entry and Cell Division

inferred← citeshttps://doi.org/10.4049/jimmunol.1700438openalex-snapshot

A Coronin 1–Dependent Decision Switch in Juvenile Mice Determines the Population of the Peripheral Naive T Cell Compartment

inferred← citeshttps://doi.org/10.4049/jimmunol.1701698openalex-snapshot

Antigen-Induced but Not Innate Memory CD8 T Cells Express NKG2D and Are Recruited to the Lung Parenchyma upon Viral Infection

inferred← citeshttps://doi.org/10.4049/jimmunol.171.10.5157openalex-snapshot

Peripheral CD4+ Lymphocytes Derived from Fetal versus Adult Thymic Precursors Differ Phenotypically and Functionally

inferred← citeshttps://doi.org/10.4049/jimmunol.171.8.4175openalex-snapshot

Ex Vivo Analysis of Thymic CD4 T Cells in Nonobese Diabetic Mice with Tetramers Generated from I-Ag7/Class II-Associated Invariant Chain Peptide Precursors

inferred← citeshttps://doi.org/10.4049/jimmunol.172.1.15openalex-snapshot

Cutting Edge: IL-7-Dependent Homeostatic Proliferation of CD8+ T Cells in Neonatal Mice Allows the Generation of Long-Lived Natural Memory T Cells

inferred← citeshttps://doi.org/10.4049/jimmunol.172.6.3391openalex-snapshot

Suppression of CD4+ T Lymphocyte Effector Functions by CD4+CD25+ Cells In Vivo

inferred← citeshttps://doi.org/10.4049/jimmunol.173.5.3084openalex-snapshot

Functional Maturation of CD4+CD25+CTLA4+CD45RA+ T Regulatory Cells in Human Neonatal T Cell Responses to Environmental Antigens/Allergens

inferred← citeshttps://doi.org/10.4049/jimmunol.174.11.6571openalex-snapshot

The Many Faces of IL-7: From Lymphopoiesis to Peripheral T Cell Maintenance

inferred← citeshttps://doi.org/10.4049/jimmunol.174.8.4606openalex-snapshot

γδ T Cell Homeostasis Is Controlled by IL-7 and IL-15 Together with Subset-Specific Factors

inferred← citeshttps://doi.org/10.4049/jimmunol.174.9.5316openalex-snapshot

A Major Role for Memory CD4 T Cells in the Control of Lymphopenia-Induced Proliferation of Naive CD4 T Cells

inferred← citeshttps://doi.org/10.4049/jimmunol.175.10.6450openalex-snapshot

Thymus-Dependent Memory Phenotype CD8 T Cells in Naive B6.H-2Kb−/−Db−/− Animals Mediate an Antigen-Specific Response against Listeria monocytogenes

inferred← citeshttps://doi.org/10.4049/jimmunol.175.2.647openalex-snapshot

E2F1 and E2F2 Are Differentially Required for Homeostasis-Driven and Antigen-Induced T Cell Proliferation In Vivo

inferred← citeshttps://doi.org/10.4049/jimmunol.177.7.4558openalex-snapshot

CD25+CD4+ Regulatory T Cells and Memory T Cells Prevent Lymphopenia-Induced Proliferation of Naive T Cells in Transient States of Lymphopenia

inferred← citeshttps://doi.org/10.4049/jimmunol.178.11.6735openalex-snapshot

An Essential Role for TNF in Modulating Thresholds for Survival, Activation, and Tolerance of CD8+ T Cells

inferred← citeshttps://doi.org/10.4049/jimmunol.178.5.2667openalex-snapshot

Murine Neonatal CD4+ Cells Are Poised for Rapid Th2 Effector-Like Function

inferred← citeshttps://doi.org/10.4049/jimmunol.181.9.5895openalex-snapshot

Pathogenic Effector T Cell Enrichment Overcomes Regulatory T Cell Control and Generates Autoimmune Gastritis

inferred← citeshttps://doi.org/10.48550/arxiv.1007.5035openalex-snapshot

A new homeostatic model of the T cell system

inferred← citeshttps://doi.org/10.64898/2026.07.03.731744openalex-snapshot

Bcl11b dose-dependently regulates positive selection of CD8 T cells to the virtual memory fate

inferred← citeshttps://doi.org/10.70675/01ba7851z8e89z4122z8d3az69b3dc44a0f8openalex-snapshot

Auto-immunité et sclérodermie systémique : effets de la modulation des lymphocytes T régulateurs dans un modèle murin

inferred← citeshttps://doi.org/10.70675/1bde1fdczc9c0z4057zb72azd892a904f814openalex-snapshot

Rôle de la profération induite par la lymphopénie dans la rupture de la tolérance périphérique des lymphocytes T CD8+

inferred← citeshttps://doi.org/10.70675/2d6ddf6az693bz4096z8988z078b5283dc9aopenalex-snapshot

Identification de nouveaux biomarqueurs permettant la caractérisation des lymphocytes T CD8 mémoires innés

inferred← citeshttps://doi.org/10.70675/f4c31cbcz110ez48dbza3eaz9a7512ef00feopenalex-snapshot

Activation of CD8+ and CD4+ T cells in response to self-antigen : from the lymphoid tissue to the target organ

inferred← citeshttps://doi.org/10.7150/thno.42943openalex-snapshot

Specific ablation of CD4+ T-cells promotes heart regeneration in juvenile mice

inferred← citeshttps://doi.org/10.7554/elife.23013openalex-snapshot

Memory CD4 T cell subsets are kinetically heterogeneous and replenished from naive T cells at high levels

inferred← citeshttps://doi.org/10.7554/elife.61639openalex-snapshot

Early life imprints the hierarchy of T cell clone sizes

inferred← citeshttps://doi.org/10.7554/elife.78168openalex-snapshot

Towards a unified model of naive T cell dynamics across the lifespan

inferred← citeshttps://doi.org/10.7936/k7vd6wf0openalex-snapshot

The Role of TCR Specificity in the Regulation of the Immune Response to Self and Commensal Antigens

inferred← citeshttps://doi.org/10.82308/6017openalex-snapshot

Novel findings on the impact of HIV infection: Interplay between T cell development and peripheral T cell homeostasis

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