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Treatment of Multiorgan Sarcoidosis With Tofacitinib
by
Damsky, William
, Obando, J. Antonio
, Young, Bryan D.
, Miller, Edward J.
, Sloan, Brett
, King, Brett
in
Biomarkers
/ Brief Report
/ Chemokines
/ Cytokines
/ Immunoglobulins
/ Immunomodulators
/ Inflammation
/ Kinases
/ Ligands
/ Lungs
/ Lymphatic system
/ Patients
/ Plasma
/ Sarcoidosis
/ Skin
/ Tumor necrosis factor-TNF
2020
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Treatment of Multiorgan Sarcoidosis With Tofacitinib
by
Damsky, William
, Obando, J. Antonio
, Young, Bryan D.
, Miller, Edward J.
, Sloan, Brett
, King, Brett
in
Biomarkers
/ Brief Report
/ Chemokines
/ Cytokines
/ Immunoglobulins
/ Immunomodulators
/ Inflammation
/ Kinases
/ Ligands
/ Lungs
/ Lymphatic system
/ Patients
/ Plasma
/ Sarcoidosis
/ Skin
/ Tumor necrosis factor-TNF
2020
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Treatment of Multiorgan Sarcoidosis With Tofacitinib
by
Damsky, William
, Obando, J. Antonio
, Young, Bryan D.
, Miller, Edward J.
, Sloan, Brett
, King, Brett
in
Biomarkers
/ Brief Report
/ Chemokines
/ Cytokines
/ Immunoglobulins
/ Immunomodulators
/ Inflammation
/ Kinases
/ Ligands
/ Lungs
/ Lymphatic system
/ Patients
/ Plasma
/ Sarcoidosis
/ Skin
/ Tumor necrosis factor-TNF
2020
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Journal Article
Treatment of Multiorgan Sarcoidosis With Tofacitinib
2020
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Overview
Objective Sarcoidosis is an idiopathic inflammatory disorder that is difficult to treat. There is accumulating evidence that constitutive activation of Janus kinase–signal transducer and activator of transcription (JAK‐STAT) signaling occurs in sarcoidosis and represents a target for treatment. Here we report the efficacy of tofacitinib, a Janus kinase (JAK) inhibitor, in a single patient with multiorgan sarcoidosis. Methods A patient with long‐standing multiorgan sarcoidosis who was unresponsive to other commonly used therapies, including methotrexate, prednisone, and tumor necrosis factor α blockade, was treated with tofacitinib. Results Tofacitinib treatment resulted in clinical remission of cutaneous sarcoidosis lesions and resolution of positron emission tomography avid lesions in internal organs after 6 months. An evaluation of lesional tissue and blood before and during treatment showed resolution of granulomatous inflammation and normalization of disease biomarkers. Conclusion This case illustrates the promise of JAK inhibition as a strategy to treat recalcitrant sarcoidosis and suggests that further study of JAK inhibitors in sarcoidosis is needed.
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