Memory T cell subsets in tuberculosis: what should we be targeting? (Q38226052)

31 August 2017

Memory T cell subsets in tuberculosis: what should we be targeting? (English)

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31 August 2017

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Diane J Ordway

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Ian Orme

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object named as

Ian M Orme

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31 August 2017

Marcela Henao-Tamayo

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31 August 2017

17 June 2014

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31 August 2017

455-461

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31 August 2017

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The effector to memory transition of CD4 T cells.

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Homeostasis of memory T cells

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Functional and genomic profiling of effector CD8 T cell subsets with distinct memory fates

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

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

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CD40L+ CD4+ memory T cells migrate in a CD62P-dependent fashion into reactive lymph nodes and license dendritic cells for T cell priming

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Chemokine receptor expression identifies Pre-T helper (Th)1, Pre-Th2, and nonpolarized cells among human CD4+ central memory T cells

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Fine-tuning CD4+ central memory T cell heterogeneity by strength of stimulation

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Expression of CXCR6 and its ligand CXCL16 in the lung in health and disease

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Characterization of a subset of antigen-specific human central memory CD4+ T lymphocytes producing effector cytokines.

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Distinct functions of antigen-specific CD4 T cells during murine Mycobacterium tuberculosis infection

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T lymphocyte surface expression of exhaustion markers as biomarkers of the efficacy of chemotherapy for tuberculosis

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

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Homeostatic proliferation and survival of naïve and memory T cells

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Antiviral CD4+ memory T cells are IL-15 dependent

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Differential In Vivo Persistence of Two Subsets of Memory Phenotype CD8 T Cells Defined by CD44 and CD122 Expression Levels

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T-cell quality in memory and protection: implications for vaccine design

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Distinct lineages of T(H)1 cells have differential capacities for memory cell generation in vivo.

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Quality and Vaccine Efficacy of CD4+ T Cell Responses Directed to Dominant and Subdominant Epitopes in ESAT-6 from Mycobacterium tuberculosis

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Half-truths and selective memory: Interferon gamma, CD4(+) T cells and protective memory against tuberculosis.

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IFN-induced attrition of CD8 T cells in the presence or absence of cognate antigen during the early stages of viral infections.

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The hypervirulent Mycobacterium tuberculosis strain HN878 induces a potent TH1 response followed by rapid down-regulation

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Memory CD4 T cells emerge from effector T-cell progenitors.

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Phenotypic definition of effector and memory T-lymphocyte subsets in mice chronically infected with Mycobacterium tuberculosis

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Expression of memory immunity in the lung following re-exposure to Mycobacterium tuberculosis.

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CD4(+) T-cell subsets that mediate immunological memory to Mycobacterium tuberculosis infection in mice

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Memory T lymphocytes generated by Mycobacterium bovis BCG vaccination reside within a CD4 CD44lo CD62 ligand(hi) population

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Th17 cells are long lived and retain a stem cell-like molecular signature

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Resident memory T cells (T(RM)) are abundant in human lung: diversity, function, and antigen specificity

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Distinct effector memory CD4+ T cell signatures in latent Mycobacterium tuberculosis infection, BCG vaccination and clinically resolved tuberculosis

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Polyfunctional Mycobacterium tuberculosis-specific effector memory CD4+ T cells at sites of pleural TB.

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Rate of reinfection tuberculosis after successful treatment is higher than rate of new tuberculosis

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Reduced frequency of memory T cells and increased Th17 responses in patients with active tuberculosis

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Memory T cells in latent Mycobacterium tuberculosis infection are directed against three antigenic islands and largely contained in a CXCR3+CCR6+ Th1 subset

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A mycolic acid-specific CD1-restricted T cell population contributes to acute and memory immune responses in human tuberculosis infection

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Lung dendritic cells imprint T cell lung homing and promote lung immunity through the chemokine receptor CCR4.

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Characterization of W-Beijing isolates of Mycobacterium tuberculosis from the Western Cape.

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Specific T cell frequency and cytokine expression profile do not correlate with protection against tuberculosis after bacillus Calmette-Guérin vaccination of newborns

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IL-23 and IL-17 in the establishment of protective pulmonary CD4+ T cell responses after vaccination and during Mycobacterium tuberculosis challenge

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Mycobacterium bovis BCG-specific Th17 cells confer partial protection against Mycobacterium tuberculosis infection in the absence of gamma interferon

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Evolution of CD4 T-cell subsets following infection of naive and memory immune mice with Mycobacterium tuberculosis

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7 January 2021

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Identifiers

DOI

10.1016/J.TUBE.2014.05.001

1 reference

31 August 2017

1 reference

PubMed ID

24993316