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

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

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

http://www.wikidata.org/entity/Q34048855

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Memory CD4 T cell subsets are kinetically heterogeneous and replenished from naive T cells at high levels.Rapid proliferation and differentiation impairs the development of memory CD8+ T cells in early life.Helios expression is a marker of T cell activation and proliferation.Role for Bcl-6 in the generation and maintenance of memory CD8+ T cells.Antigen-inexperienced memory CD8+ T cells: where they come from and why we need them.Antigen-specific peripheral shaping of the natural regulatory T cell population.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 A central role for mTOR kinase in homeostatic proliferation induced CD8+ T cell memory and tumor immunity Acute neonatal infections 'lock-in' a suboptimal CD8+ T cell repertoire with impaired recall responses.On the role of MHC class II molecules in the survival and lymphopenia-induced proliferation of peripheral CD4+ T cells.Role of T and NK cells and IL7/IL7r interactions during neonatal maturation of lymph nodes.Increased thymic output during acute measles virus infection.Human natural regulatory T cell development, suppressive function, and postthymic maturation in a humanized mouse model The concept of space and competition in immune regulation.Derivation and maintenance of virtual memory CD8 T cells.Essential role of survivin, an inhibitor of apoptosis protein, in T cell development, maturation, and homeostasis.Innate and virtual memory T cells in man.IL-7 enhances peripheral T cell reconstitution after allogeneic hematopoietic stem cell transplantation.MicroRNAs and Their Targets Are Differentially Regulated in Adult and Neonatal Mouse CD8+ T Cells 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.Hyper innate responses in neonates lead to increased morbidity and mortality after infection.Competition for self-peptide-MHC complexes and cytokines between naive and memory CD8+ T cells expressing the same or different T cell receptors.The nature of the lymphopenic environment dictates protective function of homeostatic-memory CD8+ T cells.Spontaneous proliferation, a response of naive CD4 T cells determined by the diversity of the memory cell repertoire.Virtual memory CD8 T cells display unique functional properties The antigen-specific CD8+ T cell repertoire in unimmunized mice includes memory phenotype cells bearing markers of homeostatic expansion T cell homeostasis.CD4 memory T cells: what are they and what can they do?Murine neonatal recent thymic emigrants are phenotypically and functionally distinct from adult recent thymic emigrants.Heterogeneity in the CD4 T Cell Compartment and the Variability of Neonatal Immune Responsiveness.Rapid CD8+ Function Is Critical for Protection of Neonatal Mice from an Extracellular Bacterial Enteropathogen.Lymphodepletion and homeostatic proliferation: implications for transplantation.IL-7 signaling and CD127 receptor regulation in the control of T cell homeostasis Innate memory T cells.Mechanisms of diabetic autoimmunity: II--Is diabetes a central or peripheral disorder of effector and regulatory cells?Mechanisms of diabetic autoimmunity: I--the inductive interface between islets and the immune system at onset of inflammation.In utero development of memory T cells.Tissue compartmentalization of T cell responses during early life.Reduced generation of lung tissue-resident memory T cells during infancy.Murine neonatal CD4+ cells are poised for rapid Th2 effector-like function

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P2860

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

http://www.wikidata.org/entity/Q34048855

description

2002 nî lūn-bûn

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2002 թուականի Մարտին հրատարակուած գիտական յօդուած

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2002 թվականի մարտին հրատարակված գիտական հոդված

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2002年の論文

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2002年論文

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2002年論文

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2002年論文

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2002年論文

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2002年論文

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name

Naive T cells proliferate stro ...... lf-peptide/self-MHC complexes.

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Naive T cells proliferate stro ...... lf-peptide/self-MHC complexes.

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Naive T cells proliferate stro ...... lf-peptide/self-MHC complexes.

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type

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Naive T cells proliferate stro ...... lf-peptide/self-MHC complexes.

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Naive T cells proliferate stro ...... lf-peptide/self-MHC complexes.

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Naive T cells proliferate stro ...... lf-peptide/self-MHC complexes.

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Naive T cells proliferate stro ...... lf-peptide/self-MHC complexes.

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Naive T cells proliferate stro ...... lf-peptide/self-MHC complexes.

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Proceedings of the National Academy of Sciences of the United States of America

P1476

Naive T cells proliferate stro ...... lf-peptide/self-MHC complexes.

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Armelle Le Campion

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Bruno Lucas

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Bruno Martin

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Christine Bourgeois

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Claude Pénit

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Corinne Tanchot

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Florence Lambolez

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Nicole Dautigny

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Sandrine Léaument

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P2860

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

Anergy and cytokine-mediated suppression as distinct superantigen-induced tolerance mechanisms in vivo

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

Mice lacking MHC class II molecules

T-cell function in newborn mice and humans.

Selecting and maintaining a diverse T-cell repertoire.

Neonatal immunity: how well has it grown up?

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

Homeostatic T cell proliferation: how far can T cells be activated to self-ligands?

T cell immunity in neonates.

P304

4538-4543

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scholarly article

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10.1073/PNAS.062621699

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P433

7

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99

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2002-03-26T00:00:00Z

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11447761

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11917110

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123683

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