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We are analyzing https://link.springer.com/article/10.1007/s12026-018-8989-4.

Title:
Impaired natural killer cell subset phenotypes in human obesity | Immunologic Research
Description:
Obesity is associated with alterations in functionality of immune cells, like macrophages and natural killer (NK) cells, leading to an increased risk for severe infections and several cancer types. This study aimed to examine immune cell populations and functional NK cell parameters focusing on NK cell subset phenotypes in normal-weight and obese humans. Therefore, peripheral blood mononuclear cells (PBMCs) were isolated from normal-weight and obese individuals and analyzed by flow cytometry. Results show no significant changes in the frequency of monocytes, B lymphocytes, or NKT cells but a significantly increased frequency of T lymphocytes in obesity. The frequency of total NK cells was unaltered, whereas the number of low cytotoxic CD56bright NK cell subset was increased, and the number of high cytotoxic CD56dim NK cell subset was decreased in obese subjects. In addition, the frequency of CD56bright NK cells expressing the activating NK cell receptor NKG2D as well as intracellular interferon (IFN)-γ was elevated in the obese study group. In contrast, the frequency of NKG2D- and IFN-γ-positive CD56dim NK cells was lower in obesity compared to normal-weight individuals. Moreover, the expression of the activation marker CD69 was decreased in NK cells, which can be attributed to a reduction of CD69-positive CD56dim NK cells in obese subjects. In conclusion, data reveal an impaired NK cell phenotype and NK cell subset alterations in obese individuals. This NK cell dysfunction might be one link to the higher cancer risk and the elevated susceptibility for viral infections in obesity.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Science
  • Education
  • Telecommunications

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
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How Does Link.springer.com Make Money? {💸}

We can't see how the site brings in money.

Some websites aren't about earning revenue; they're built to connect communities or raise awareness. There are numerous motivations behind creating websites. This might be one of them. Link.springer.com might have a hidden revenue stream, but it's not something we can detect.

Keywords {🔍}

cells, cell, obese, pubmed, article, obesity, google, scholar, expression, cddim, cdbright, normalweight, study, cas, subjects, individuals, data, leptin, frequency, human, receptor, bmi, natural, analyses, killer, subsets, increased, subset, pbmcs, nkgd, fig, results, immune, total, body, immunol, significantly, blood, group, phenotype, correlation, central, decreased, ifnγ, compared, studies, conjugated, impaired, functionality, humans,

Topics {✒️}

anticoagulant ethylene-diamine-tetra-acetic acid pd-l1/nkg2d ligand levels ifn-γ-expressing nk cells leptin modulates dose-dependently human nk-cell cytokine article download pdf abundant ifn-γ production nkg2d-expressing nk cells il-6/stat3-dependent induction nkg2d-positive nk cells cytokine-mediated immunoregulatory effect cd69-positive nk cells long-term proliferation population-based cohort study natural killer cells ifn-γ antibody conjugated cd69-triggered erk activation nk cell subset full access investigations analyzing degranulation cd3 pe-cy7 antibody nk cell lines observed comparing normal-weight o'shea db analyze plasma concentrations normal-weight study group expressing nk cells target cell recognition tumor necrosis factor spleen lymphocyte functions nk cell subpopulations impaired immune response lower cd56dim/cd56bright ratio human nk cells high leptin concentrations cell subsets showed nk cell subsets diet-induced obese mice ifn-γ expression cell surface staining privacy choices/manage cookies nk cell dysfunction nkg2d expressing cd56bright naffah de souza ifn-γ secretion cd56dim subset based diet-induced obese rats plasma leptin levels obesity-related parameters altered immune responses

Questions {❓}

  • Are natural killer cells protecting the metabolically healthy obese patient?

Schema {🗺️}

WebPage:
      mainEntity:
         headline:Impaired natural killer cell subset phenotypes in human obesity
         description:Obesity is associated with alterations in functionality of immune cells, like macrophages and natural killer (NK) cells, leading to an increased risk for severe infections and several cancer types. This study aimed to examine immune cell populations and functional NK cell parameters focusing on NK cell subset phenotypes in normal-weight and obese humans. Therefore, peripheral blood mononuclear cells (PBMCs) were isolated from normal-weight and obese individuals and analyzed by flow cytometry. Results show no significant changes in the frequency of monocytes, B lymphocytes, or NKT cells but a significantly increased frequency of T lymphocytes in obesity. The frequency of total NK cells was unaltered, whereas the number of low cytotoxic CD56bright NK cell subset was increased, and the number of high cytotoxic CD56dim NK cell subset was decreased in obese subjects. In addition, the frequency of CD56bright NK cells expressing the activating NK cell receptor NKG2D as well as intracellular interferon (IFN)-γ was elevated in the obese study group. In contrast, the frequency of NKG2D- and IFN-γ-positive CD56dim NK cells was lower in obesity compared to normal-weight individuals. Moreover, the expression of the activation marker CD69 was decreased in NK cells, which can be attributed to a reduction of CD69-positive CD56dim NK cells in obese subjects. In conclusion, data reveal an impaired NK cell phenotype and NK cell subset alterations in obese individuals. This NK cell dysfunction might be one link to the higher cancer risk and the elevated susceptibility for viral infections in obesity.
         datePublished:2018-03-20T00:00:00Z
         dateModified:2018-03-20T00:00:00Z
         pageStart:234
         pageEnd:244
         sameAs:https://doi.org/10.1007/s12026-018-8989-4
         keywords:
            Human natural killer cells
            Immune cell functions
            Adipocytokines
            Obesity
            Immunology
            Allergology
            Medicine/Public Health
            general
            Internal Medicine
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                     address:
                        name:Department of Anatomy and Cell Biology, Faculty of Medicine, Martin Luther University Halle-Wittenberg, Halle/Saale, Germany
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ScholarlyArticle:
      headline:Impaired natural killer cell subset phenotypes in human obesity
      description:Obesity is associated with alterations in functionality of immune cells, like macrophages and natural killer (NK) cells, leading to an increased risk for severe infections and several cancer types. This study aimed to examine immune cell populations and functional NK cell parameters focusing on NK cell subset phenotypes in normal-weight and obese humans. Therefore, peripheral blood mononuclear cells (PBMCs) were isolated from normal-weight and obese individuals and analyzed by flow cytometry. Results show no significant changes in the frequency of monocytes, B lymphocytes, or NKT cells but a significantly increased frequency of T lymphocytes in obesity. The frequency of total NK cells was unaltered, whereas the number of low cytotoxic CD56bright NK cell subset was increased, and the number of high cytotoxic CD56dim NK cell subset was decreased in obese subjects. In addition, the frequency of CD56bright NK cells expressing the activating NK cell receptor NKG2D as well as intracellular interferon (IFN)-γ was elevated in the obese study group. In contrast, the frequency of NKG2D- and IFN-γ-positive CD56dim NK cells was lower in obesity compared to normal-weight individuals. Moreover, the expression of the activation marker CD69 was decreased in NK cells, which can be attributed to a reduction of CD69-positive CD56dim NK cells in obese subjects. In conclusion, data reveal an impaired NK cell phenotype and NK cell subset alterations in obese individuals. This NK cell dysfunction might be one link to the higher cancer risk and the elevated susceptibility for viral infections in obesity.
      datePublished:2018-03-20T00:00:00Z
      dateModified:2018-03-20T00:00:00Z
      pageStart:234
      pageEnd:244
      sameAs:https://doi.org/10.1007/s12026-018-8989-4
      keywords:
         Human natural killer cells
         Immune cell functions
         Adipocytokines
         Obesity
         Immunology
         Allergology
         Medicine/Public Health
         general
         Internal Medicine
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         https://media.springernature.com/lw1200/springer-static/image/art%3A10.1007%2Fs12026-018-8989-4/MediaObjects/12026_2018_8989_Fig2_HTML.gif
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                  name:Martin Luther University Halle-Wittenberg
                  address:
                     name:Department of Anatomy and Cell Biology, Faculty of Medicine, Martin Luther University Halle-Wittenberg, Halle/Saale, Germany
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                  name:University Hospital of Martin Luther University Halle-Wittenberg
                  address:
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                  name:Martin Luther University Halle-Wittenberg
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                     name:Department of Anatomy and Cell Biology, Faculty of Medicine, Martin Luther University Halle-Wittenberg, Halle/Saale, Germany
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                     name:Department of Anatomy and Cell Biology, Faculty of Medicine, Martin Luther University Halle-Wittenberg, Halle/Saale, Germany
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                     name:Department of Anatomy and Cell Biology, Faculty of Medicine, Martin Luther University Halle-Wittenberg, Halle/Saale, Germany
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         type:PostalAddress
      name:University Hospital of Martin Luther University Halle-Wittenberg
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         type:PostalAddress
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      address:
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         type:PostalAddress
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      affiliation:
            name:Martin Luther University Halle-Wittenberg
            address:
               name:Department of Anatomy and Cell Biology, Faculty of Medicine, Martin Luther University Halle-Wittenberg, Halle/Saale, Germany
               type:PostalAddress
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      email:[email protected]
      name:Janine Jahn
      affiliation:
            name:Martin Luther University Halle-Wittenberg
            address:
               name:Department of Anatomy and Cell Biology, Faculty of Medicine, Martin Luther University Halle-Wittenberg, Halle/Saale, Germany
               type:PostalAddress
            type:Organization
      name:Alexander Zipprich
      affiliation:
            name:University Hospital of Martin Luther University Halle-Wittenberg
            address:
               name:Clinic of Internal Medicine I, University Hospital of Martin Luther University Halle-Wittenberg, Halle/Saale, Germany
               type:PostalAddress
            type:Organization
      name:Inge Pahlow
      affiliation:
            name:Martin Luther University Halle-Wittenberg
            address:
               name:Department of Anatomy and Cell Biology, Faculty of Medicine, Martin Luther University Halle-Wittenberg, Halle/Saale, Germany
               type:PostalAddress
            type:Organization
      name:Julia Spielmann
      affiliation:
            name:Martin Luther University Halle-Wittenberg
            address:
               name:Department of Anatomy and Cell Biology, Faculty of Medicine, Martin Luther University Halle-Wittenberg, Halle/Saale, Germany
               type:PostalAddress
            type:Organization
      name:Heike Kielstein
      affiliation:
            name:Martin Luther University Halle-Wittenberg
            address:
               name:Department of Anatomy and Cell Biology, Faculty of Medicine, Martin Luther University Halle-Wittenberg, Halle/Saale, Germany
               type:PostalAddress
            type:Organization
PostalAddress:
      name:Department of Anatomy and Cell Biology, Faculty of Medicine, Martin Luther University Halle-Wittenberg, Halle/Saale, Germany
      name:Department of Anatomy and Cell Biology, Faculty of Medicine, Martin Luther University Halle-Wittenberg, Halle/Saale, Germany
      name:Clinic of Internal Medicine I, University Hospital of Martin Luther University Halle-Wittenberg, Halle/Saale, Germany
      name:Department of Anatomy and Cell Biology, Faculty of Medicine, Martin Luther University Halle-Wittenberg, Halle/Saale, Germany
      name:Department of Anatomy and Cell Biology, Faculty of Medicine, Martin Luther University Halle-Wittenberg, Halle/Saale, Germany
      name:Department of Anatomy and Cell Biology, Faculty of Medicine, Martin Luther University Halle-Wittenberg, Halle/Saale, Germany

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