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Respiratory Medicine
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    • Focus on Sarcoidosis
    • Arger, Nicholas KRemove Arger, Nicholas K filter
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    Article Type

    • Research Article2

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    • Last 5 Years2
    Please choose a date range between 2019 and 2019.

    Author

    • Koth, Laura L2
    • Woodruff, Prescott G2
    • Allen, Isabel E1
    • Benn, Bryan S1
    • Ho, Melissa1
    • Ho, Melissa E1

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    • Respiratory Medicine2

    Keyword

    • Chemokine2
    • CXCL102
    • CXCL112
    • CXCL92
    • Interferon-gamma2
    • Sarcoidosis2

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    Focus on Sarcoidosis

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    • Research Article
      Open Archive

      CXCL9 and CXCL10 are differentially associated with systemic organ involvement and pulmonary disease severity in sarcoidosis

      Respiratory Medicine
      Vol. 161105822Published online: November 20, 2019
      • Nicholas K. Arger
      • Melissa E. Ho
      • Isabel E. Allen
      • Bryan S. Benn
      • Prescott G. Woodruff
      • Laura L. Koth
      Cited in Scopus: 10
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        Sarcoidosis is a granulomatous inflammatory disease with limited blood markers to predict outcomes. The interferon-gamma (IFN-γ)-inducible chemotactic cytokines (chemokines), CXCL9 and CXCL10, are both increased in sarcoidosis patients, yet they possess important molecular differences. Our study determined if serum chemokines correlated with different aspects of disease severity.
        CXCL9 and CXCL10 are differentially associated with systemic organ involvement and pulmonary disease severity in sarcoidosis
      • Research Article
        Open Archive

        Serum CXCL11 correlates with pulmonary outcomes and disease burden in sarcoidosis

        Respiratory Medicine
        Vol. 152p89–96Published online: April 16, 2019
        • Nicholas K. Arger
        • Melissa Ho
        • Prescott G. Woodruff
        • Laura L. Koth
        Cited in Scopus: 18
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          Sarcoidosis is a systemic granulomatous disease of unknown etiology that affects the lungs in 90% of patients, but has a wide range of disease manifestations and outcomes including chronic and progressive courses. Noninvasive biomarkers are needed to assess these outcomes and guide decisions for long term monitoring and treatment. Interferon-gamma (IFN-γ)-inducible chemotactic cytokines (chemokines), CXCL9, CXCL10 and CXCL11, show promise in this regard because they have been implicated in the pathogenesis of and reflect the burden of granulomatous inflammation.
          Serum CXCL11 correlates with pulmonary outcomes and disease burden in sarcoidosis
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