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Th1 responses in vivo require cell-specific provision of OX40L dictated by environmental cues
by
Gaspal, Fabrina
, Willis, Claire
, Vyse, Timothy
, Gerard, Audrey
, MacDonald, Andrew S.
, Romagnani, Chiara
, Halford, Emily E.
, Bevington, Sarah L.
, Fiancette, Remi
, Rückert, Timo
, Gajdasik, Dominika W.
, Withers, David R.
, Dutton, Emma E.
, Botto, Marina
in
13/106
/ 13/21
/ 14/35
/ 49/31
/ 631/250
/ 631/326
/ 64
/ 64/60
/ Animals
/ CD4 antigen
/ Cell Communication
/ Cellular Microenvironment
/ Chronic infection
/ Crosstalk
/ Cues
/ Cytokines
/ Dendritic cells
/ Dendritic Cells - drug effects
/ Dendritic Cells - metabolism
/ Disseminated infection
/ Humanities and Social Sciences
/ Humans
/ Immunology
/ Infections
/ Inflammatory diseases
/ Interferon-gamma - biosynthesis
/ Interleukin-12 - pharmacology
/ Intestine
/ Intestines - cytology
/ Ki-1 Antigen - metabolism
/ Killer Cells, Natural - drug effects
/ Killer Cells, Natural - metabolism
/ Listeria
/ Listeria monocytogenes
/ Listeria monocytogenes - physiology
/ Lymphocytes
/ Lymphocytes B
/ Lymphocytes T
/ Lymphoid cells
/ Mice, Inbred C57BL
/ multidisciplinary
/ OX40 Ligand - metabolism
/ Ox40L protein
/ Peptides
/ Receptors, CXCR5 - metabolism
/ Receptors, OX40 - metabolism
/ Science
/ Science (multidisciplinary)
/ Signal transduction
/ Spleen - metabolism
/ T cell receptors
/ Th1 Cells - immunology
/ Tumor necrosis factor-TNF
/ Up-Regulation - drug effects
/ γ-Interferon
2020
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Th1 responses in vivo require cell-specific provision of OX40L dictated by environmental cues
by
Gaspal, Fabrina
, Willis, Claire
, Vyse, Timothy
, Gerard, Audrey
, MacDonald, Andrew S.
, Romagnani, Chiara
, Halford, Emily E.
, Bevington, Sarah L.
, Fiancette, Remi
, Rückert, Timo
, Gajdasik, Dominika W.
, Withers, David R.
, Dutton, Emma E.
, Botto, Marina
in
13/106
/ 13/21
/ 14/35
/ 49/31
/ 631/250
/ 631/326
/ 64
/ 64/60
/ Animals
/ CD4 antigen
/ Cell Communication
/ Cellular Microenvironment
/ Chronic infection
/ Crosstalk
/ Cues
/ Cytokines
/ Dendritic cells
/ Dendritic Cells - drug effects
/ Dendritic Cells - metabolism
/ Disseminated infection
/ Humanities and Social Sciences
/ Humans
/ Immunology
/ Infections
/ Inflammatory diseases
/ Interferon-gamma - biosynthesis
/ Interleukin-12 - pharmacology
/ Intestine
/ Intestines - cytology
/ Ki-1 Antigen - metabolism
/ Killer Cells, Natural - drug effects
/ Killer Cells, Natural - metabolism
/ Listeria
/ Listeria monocytogenes
/ Listeria monocytogenes - physiology
/ Lymphocytes
/ Lymphocytes B
/ Lymphocytes T
/ Lymphoid cells
/ Mice, Inbred C57BL
/ multidisciplinary
/ OX40 Ligand - metabolism
/ Ox40L protein
/ Peptides
/ Receptors, CXCR5 - metabolism
/ Receptors, OX40 - metabolism
/ Science
/ Science (multidisciplinary)
/ Signal transduction
/ Spleen - metabolism
/ T cell receptors
/ Th1 Cells - immunology
/ Tumor necrosis factor-TNF
/ Up-Regulation - drug effects
/ γ-Interferon
2020
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Th1 responses in vivo require cell-specific provision of OX40L dictated by environmental cues
by
Gaspal, Fabrina
, Willis, Claire
, Vyse, Timothy
, Gerard, Audrey
, MacDonald, Andrew S.
, Romagnani, Chiara
, Halford, Emily E.
, Bevington, Sarah L.
, Fiancette, Remi
, Rückert, Timo
, Gajdasik, Dominika W.
, Withers, David R.
, Dutton, Emma E.
, Botto, Marina
in
13/106
/ 13/21
/ 14/35
/ 49/31
/ 631/250
/ 631/326
/ 64
/ 64/60
/ Animals
/ CD4 antigen
/ Cell Communication
/ Cellular Microenvironment
/ Chronic infection
/ Crosstalk
/ Cues
/ Cytokines
/ Dendritic cells
/ Dendritic Cells - drug effects
/ Dendritic Cells - metabolism
/ Disseminated infection
/ Humanities and Social Sciences
/ Humans
/ Immunology
/ Infections
/ Inflammatory diseases
/ Interferon-gamma - biosynthesis
/ Interleukin-12 - pharmacology
/ Intestine
/ Intestines - cytology
/ Ki-1 Antigen - metabolism
/ Killer Cells, Natural - drug effects
/ Killer Cells, Natural - metabolism
/ Listeria
/ Listeria monocytogenes
/ Listeria monocytogenes - physiology
/ Lymphocytes
/ Lymphocytes B
/ Lymphocytes T
/ Lymphoid cells
/ Mice, Inbred C57BL
/ multidisciplinary
/ OX40 Ligand - metabolism
/ Ox40L protein
/ Peptides
/ Receptors, CXCR5 - metabolism
/ Receptors, OX40 - metabolism
/ Science
/ Science (multidisciplinary)
/ Signal transduction
/ Spleen - metabolism
/ T cell receptors
/ Th1 Cells - immunology
/ Tumor necrosis factor-TNF
/ Up-Regulation - drug effects
/ γ-Interferon
2020
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Th1 responses in vivo require cell-specific provision of OX40L dictated by environmental cues
Journal Article
Th1 responses in vivo require cell-specific provision of OX40L dictated by environmental cues
2020
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Overview
The OX40-OX40L pathway provides crucial co-stimulatory signals for CD4 T cell responses, however the precise cellular interactions critical for OX40L provision in vivo and when these occur, remains unclear. Here, we demonstrate that provision of OX40L by dendritic cells (DCs), but not T cells, B cells nor group 3 innate lymphoid cells (ILC3s), is critical specifically for the effector Th1 response to an acute systemic infection with Listeria monocytogenes (Lm). OX40L expression by DCs is regulated by cross-talk with NK cells, with IFNγ signalling to the DC to enhance OX40L in a mechanism conserved in both mouse and human DCs. Strikingly, DC expression of OX40L is redundant in a chronic intestinal Th1 response and expression by ILC3s is necessary. Collectively these data reveal tissue specific compartmentalisation of the cellular provision of OX40L and define a mechanism controlling DC expression of OX40L in vivo.
The OX40-OX40L axis is a crucial component of the costimulatory requirement of CD4 T cell responses. Here, the authors show context and cell type specific expression of OX40L for driving Th1 cell generation during acute and chronic models of infection.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
Subject
/ 13/21
/ 14/35
/ 49/31
/ 631/250
/ 631/326
/ 64
/ 64/60
/ Animals
/ Cues
/ Dendritic Cells - drug effects
/ Dendritic Cells - metabolism
/ Humanities and Social Sciences
/ Humans
/ Interferon-gamma - biosynthesis
/ Interleukin-12 - pharmacology
/ Killer Cells, Natural - drug effects
/ Killer Cells, Natural - metabolism
/ Listeria
/ Listeria monocytogenes - physiology
/ Peptides
/ Receptors, CXCR5 - metabolism
/ Receptors, OX40 - metabolism
/ Science
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