Abstract
Dendritic cells (DCs) play the central role in the priming of naive T cells and the differentiation of unique effector T cells. In this study, using lung tissues and blood from both humans and humanized mice, we analyzed the response of human CD1c(+) and CD141(+) DC subsets to live-attenuated influenza virus. Specifically, we analyzed the type of CD4(+) T cell immunity elicited by live-attenuated influenza virus-exposed DCs. Both DC subsets induce proliferation of allogeneic naive CD4(+) T cells with the capacity to secrete IFN-γ. However, CD141(+) DCs are uniquely able to induce the differentiation of IL-4- and IL-13-producing CD4(+) T cells. CD141(+) DCs induce IL-4- and IL-13-secreting CD4(+) T cells through OX40 ligand. Thus, CD141(+) DCs demonstrate remarkable plasticity in guiding adaptive immune responses.
Copyright © 2014 by The American Association of Immunologists, Inc.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Antigens, CD1 / metabolism
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Antigens, Surface / metabolism*
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CD4-Positive T-Lymphocytes / cytology
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CD4-Positive T-Lymphocytes / immunology*
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CD4-Positive T-Lymphocytes / metabolism
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CD40 Antigens / metabolism
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Cell Differentiation
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Cells, Cultured
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Cytokines / biosynthesis*
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Dendritic Cells / immunology*
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Dendritic Cells / metabolism
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Glycoproteins / metabolism
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Humans
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Immunophenotyping
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Lung / immunology
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Lung / metabolism
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Lung / virology
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Lymphocyte Activation / immunology
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Mice
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Mice, Knockout
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OX40 Ligand / metabolism
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Orthomyxoviridae / immunology
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Phenotype
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Signal Transduction
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Th2 Cells / immunology
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Th2 Cells / metabolism
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Thrombomodulin
Substances
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Antigens, CD1
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Antigens, Surface
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CD1C protein, human
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CD40 Antigens
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Cytokines
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Glycoproteins
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OX40 Ligand
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THBD protein, human
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Thrombomodulin