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 |
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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. |
Author_xml | – sequence: 1 givenname: Adrian F. surname: Sagebiel fullname: Sagebiel, Adrian F. organization: Department of Virus Immunology, Heinrich Pette Institute, Leibniz Institute for Experimental Virology – sequence: 2 givenname: Fenja surname: Steinert fullname: Steinert, Fenja organization: Department of Virus Immunology, Heinrich Pette Institute, Leibniz Institute for Experimental Virology – sequence: 3 givenname: Sebastian surname: Lunemann fullname: Lunemann, Sebastian organization: Department of Virus Immunology, Heinrich Pette Institute, Leibniz Institute for Experimental Virology – sequence: 4 givenname: Christian surname: Körner fullname: Körner, Christian organization: Department of Virus Immunology, Heinrich Pette Institute, Leibniz Institute for Experimental Virology – sequence: 5 givenname: Renée R. C. E. surname: Schreurs fullname: Schreurs, Renée R. C. E. organization: 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 – sequence: 6 givenname: Marcus surname: Altfeld fullname: Altfeld, Marcus organization: Department of Virus Immunology, Heinrich Pette Institute, Leibniz Institute for Experimental Virology – sequence: 7 givenname: Daniel surname: Perez fullname: Perez, Daniel organization: Department of General, Visceral and Thoracic Surgery, University Medical Center Hamburg-Eppendorf – sequence: 8 givenname: Konrad surname: Reinshagen fullname: Reinshagen, Konrad organization: Department of Pediatric Surgery, University Medical Center Hamburg-Eppendorf – sequence: 9 givenname: Madeleine J. surname: Bunders fullname: Bunders, Madeleine J. email: madeleine.bunders@leibniz-hpi.de 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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Title | Tissue-resident Eomes+ NK cells are the major innate lymphoid cell population in human infant intestine |
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