Tissue-resident Eomes+ NK cells are the major innate lymphoid cell population in human infant intestine

Innate lymphoid cells (ILC), including natural killer (NK) cells, are implicated in host-defense and tissue-growth. However, the composition and kinetics of NK cells in the intestine during the first year of life, when infants are first broadly exposed to exogenous antigens, are still unclear. Here...

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Published in:Nature communications Vol. 10; no. 1; p. 975
Main Authors: Sagebiel, Adrian F., Steinert, Fenja, Lunemann, Sebastian, Körner, Christian, Schreurs, Renée R. C. E., Altfeld, Marcus, Perez, Daniel, Reinshagen, Konrad, Bunders, Madeleine J.
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Published: London Nature Publishing Group UK 28-02-2019
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Abstract Innate lymphoid cells (ILC), including natural killer (NK) cells, are implicated in host-defense and tissue-growth. However, the composition and kinetics of NK cells in the intestine during the first year of life, when infants are first broadly exposed to exogenous antigens, are still unclear. Here we show that CD103 + NK cells are the major ILC population in the small intestines of infants. When compared to adult intestinal NK cells, infant intestinal NK cells exhibit a robust effector phenotype, characterized by Eomes, perforin and granzyme B expression, and superior degranulation capacity. Absolute intestinal NK cell numbers decrease gradually during the first year of life, coinciding with an influx of intestinal Eomes + T cells; by contrast, epithelial NKp44 + CD69 + NK cells with less cytotoxic capacity persist in adults. In conclusion, NK cells are abundant in infant intestines, where they can provide effector functions while Eomes + T cell responses mature. Innate lymphoid cells (ILC), including natural killer (NK) cells, are important innate immune regulators. Here the authors show that, in human infant intestines, CD103 + Eomes + NK cells are the predominant ILC population, but are replaced gradually by Eomes + T cells, while NKp44 + NK cells persist in adult intestines.
AbstractList Innate lymphoid cells (ILC), including natural killer (NK) cells, are important innate immune regulators. Here the authors show that, in human infant intestines, CD103+Eomes+ NK cells are the predominant ILC population, but are replaced gradually by Eomes+ T cells, while NKp44+ NK cells persist in adult intestines.
Innate lymphoid cells (ILC), including natural killer (NK) cells, are implicated in host-defense and tissue-growth. However, the composition and kinetics of NK cells in the intestine during the first year of life, when infants are first broadly exposed to exogenous antigens, are still unclear. Here we show that CD103+ NK cells are the major ILC population in the small intestines of infants. When compared to adult intestinal NK cells, infant intestinal NK cells exhibit a robust effector phenotype, characterized by Eomes, perforin and granzyme B expression, and superior degranulation capacity. Absolute intestinal NK cell numbers decrease gradually during the first year of life, coinciding with an influx of intestinal Eomes+ T cells; by contrast, epithelial NKp44+CD69+ NK cells with less cytotoxic capacity persist in adults. In conclusion, NK cells are abundant in infant intestines, where they can provide effector functions while Eomes+ T cell responses mature.Innate lymphoid cells (ILC), including natural killer (NK) cells, are important innate immune regulators. Here the authors show that, in human infant intestines, CD103+Eomes+ NK cells are the predominant ILC population, but are replaced gradually by Eomes+ T cells, while NKp44+ NK cells persist in adult intestines.
Innate lymphoid cells (ILC), including natural killer (NK) cells, are implicated in host-defense and tissue-growth. However, the composition and kinetics of NK cells in the intestine during the first year of life, when infants are first broadly exposed to exogenous antigens, are still unclear. Here we show that CD103 + NK cells are the major ILC population in the small intestines of infants. When compared to adult intestinal NK cells, infant intestinal NK cells exhibit a robust effector phenotype, characterized by Eomes, perforin and granzyme B expression, and superior degranulation capacity. Absolute intestinal NK cell numbers decrease gradually during the first year of life, coinciding with an influx of intestinal Eomes + T cells; by contrast, epithelial NKp44 + CD69 + NK cells with less cytotoxic capacity persist in adults. In conclusion, NK cells are abundant in infant intestines, where they can provide effector functions while Eomes + T cell responses mature.
Innate lymphoid cells (ILC), including natural killer (NK) cells, are implicated in host-defense and tissue-growth. However, the composition and kinetics of NK cells in the intestine during the first year of life, when infants are first broadly exposed to exogenous antigens, are still unclear. Here we show that CD103 + NK cells are the major ILC population in the small intestines of infants. When compared to adult intestinal NK cells, infant intestinal NK cells exhibit a robust effector phenotype, characterized by Eomes, perforin and granzyme B expression, and superior degranulation capacity. Absolute intestinal NK cell numbers decrease gradually during the first year of life, coinciding with an influx of intestinal Eomes + T cells; by contrast, epithelial NKp44 + CD69 + NK cells with less cytotoxic capacity persist in adults. In conclusion, NK cells are abundant in infant intestines, where they can provide effector functions while Eomes + T cell responses mature. Innate lymphoid cells (ILC), including natural killer (NK) cells, are important innate immune regulators. Here the authors show that, in human infant intestines, CD103 + Eomes + NK cells are the predominant ILC population, but are replaced gradually by Eomes + T cells, while NKp44 + NK cells persist in adult intestines.
Innate lymphoid cells (ILC), including natural killer (NK) cells, are implicated in host-defense and tissue-growth. However, the composition and kinetics of NK cells in the intestine during the first year of life, when infants are first broadly exposed to exogenous antigens, are still unclear. Here we show that CD103 NK cells are the major ILC population in the small intestines of infants. When compared to adult intestinal NK cells, infant intestinal NK cells exhibit a robust effector phenotype, characterized by Eomes, perforin and granzyme B expression, and superior degranulation capacity. Absolute intestinal NK cell numbers decrease gradually during the first year of life, coinciding with an influx of intestinal Eomes T cells; by contrast, epithelial NKp44 CD69 NK cells with less cytotoxic capacity persist in adults. In conclusion, NK cells are abundant in infant intestines, where they can provide effector functions while Eomes T cell responses mature.
ArticleNumber 975
Author Perez, Daniel
Sagebiel, Adrian F.
Lunemann, Sebastian
Bunders, Madeleine J.
Reinshagen, Konrad
Steinert, Fenja
Altfeld, Marcus
Körner, Christian
Schreurs, Renée R. C. E.
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  organization: Department of Virus Immunology, Heinrich Pette Institute, Leibniz Institute for Experimental Virology, Department of Experimental Immunology, Amsterdam Infection & Immunity Institute, Amsterdam University Medical Center, University of Amsterdam, Department of Pediatrics, Emma Children’s Hospital, Amsterdam University Medical Center, University of Amsterdam
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Snippet Innate lymphoid cells (ILC), including natural killer (NK) cells, are implicated in host-defense and tissue-growth. However, the composition and kinetics of NK...
Innate lymphoid cells (ILC), including natural killer (NK) cells, are important innate immune regulators. Here the authors show that, in human infant...
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SubjectTerms 13/1
13/31
631/250/1619/382
631/250/2504/2506
631/250/347
692/4020/2741/520
Adult
Adults
Aged
Antigens
Antigens, CD - metabolism
Babies
CD103 antigen
CD69 antigen
Cytotoxicity
Degranulation
Effector cells
Granzyme B
Granzymes - metabolism
Humanities and Social Sciences
Humans
Immunity, Innate
Immunophenotyping
Infant
Infants
Integrin alpha Chains - metabolism
Intestine
Intestines - cytology
Intestines - growth & development
Intestines - immunology
Killer Cells, Natural - classification
Killer Cells, Natural - immunology
Killer Cells, Natural - metabolism
Kinetics
Lymphocytes
Lymphocytes T
Lymphoid cells
Middle Aged
multidisciplinary
Natural killer cells
NK Cell Lectin-Like Receptor Subfamily C - metabolism
Perforin
Perforin - metabolism
Phenotypes
Science
Science (multidisciplinary)
T-Box Domain Proteins - metabolism
Tissue Distribution
Tissues
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Title Tissue-resident Eomes+ NK cells are the major innate lymphoid cell population in human infant intestine
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