Downloads provided by UsageCounts
Autoimmune polyendocrine syndrome type 1 (APS-1) is a life-threatening, autosomal recessive syndrome caused by autoimmune regulator (AIRE) deficiency. In APS-1, self-reactive T cells escape thymic negative selection, infiltrate organs, and drive autoimmune injury. The effector mechanisms governing T-cell-mediated damage in APS-1 remain poorly understood.We examined whether APS-1 could be classified as a disease mediated by interferon-γ. We first assessed patients with APS-1 who were participating in a prospective natural history study and evaluated mRNA and protein expression in blood and tissues. We then examined the pathogenic role of interferon-γ using Aire-/-Ifng-/- mice and Aire-/- mice treated with the Janus kinase (JAK) inhibitor ruxolitinib. On the basis of our findings, we used ruxolitinib to treat five patients with APS-1 and assessed clinical, immunologic, histologic, transcriptional, and autoantibody responses.Patients with APS-1 had enhanced interferon-γ responses in blood and in all examined autoimmunity-affected tissues. Aire-/- mice had selectively increased interferon-γ production by T cells and enhanced interferon-γ, phosphorylated signal transducer and activator of transcription 1 (pSTAT1), and CXCL9 signals in multiple organs. Ifng ablation or ruxolitinib-induced JAK-STAT blockade in Aire-/- mice normalized interferon-γ responses and averted T-cell infiltration and damage in organs. Ruxolitinib treatment of five patients with APS-1 led to decreased levels of T-cell-derived interferon-γ, normalized interferon-γ and CXCL9 levels, and remission of alopecia, oral candidiasis, nail dystrophy, gastritis, enteritis, arthritis, Sjögren's-like syndrome, urticaria, and thyroiditis. No serious adverse effects from ruxolitinib were identified in these patients.Our findings indicate that APS-1, which is caused by AIRE deficiency, is characterized by excessive, multiorgan interferon-γ-mediated responses. JAK inhibition with ruxolitinib in five patients showed promising results. (Funded by the National Institute of Allergy and Infectious Diseases and others.).
Male, MESH: AIRE Protein / genetics, [SDV]Life Sciences [q-bio], T-Lymphocytes, Pilot Projects, MESH: AIRE Protein / immunology, Pediatrics, Chemokine CXCL9, MESH: Pyrimidines / therapeutic use, Mice, MESH: Interferon-gamma / genetics, Endocrinology, MESH: Pyrazoles / pharmacology, MESH: Child, MESH: Animals, MESH: Janus Kinase Inhibitors / therapeutic use, Clinical Medicine General, Child, Polyendocrinopathies, Autoimmune, Mice, Knockout, MESH: Middle Aged, Gastroenterology General, Gastroenterology, Inflammatory Disease, AIRE Protein, Genetics General, Middle Aged, [SDV] Life Sciences [q-bio], MESH: Transcription Factors / immunology, Pediatrics General, Female, Rheumatology General, Childhood Diseases, MESH: Interferon-gamma / immunology, Adult, MESH: T-Lymphocytes / immunology, MESH: Chemokine CXCL9 / genetics, MESH: Pyrazoles / therapeutic use, Adolescent, Knockout, Thyroid Disease, MESH: Autoantibodies / immunology, 610, T-Cells, Dermatology, MESH: Transcription Factors / genetics, Autoimmune Disease, Dermatology General, MESH: Polyendocrinopathies, Allergy/Immunology General, Allergy/Immunology, MESH: AIRE Protein / deficiency, Interferon-gamma, Adolescent Medicine, Rheumatology, Autoimmune / genetics, Outpatient-Based Clinical Medicine, 616, Nitriles, Genetics, Animals, Humans, Janus Kinase Inhibitors, Adrenal Disease, MESH: Mice, MESH: Autoantibodies / blood, MESH: Nitriles / therapeutic use, Autoantibodies, MESH: Adolescent, MESH: Humans, Animal, Inflammatory Bowel Disease, Immunity, Autoimmune / immunology, MESH: Adult, Endocrinology General, MESH: Pilot Projects, MESH: Male, Disease Models, Animal, Pyrimidines, Polyendocrinopathies, Disease Models, Autoimmune / drug therapy, Pyrazoles, MESH: Disease Models, Clinical Medicine, MESH: Female, Autoimmune, Transcription Factors
Male, MESH: AIRE Protein / genetics, [SDV]Life Sciences [q-bio], T-Lymphocytes, Pilot Projects, MESH: AIRE Protein / immunology, Pediatrics, Chemokine CXCL9, MESH: Pyrimidines / therapeutic use, Mice, MESH: Interferon-gamma / genetics, Endocrinology, MESH: Pyrazoles / pharmacology, MESH: Child, MESH: Animals, MESH: Janus Kinase Inhibitors / therapeutic use, Clinical Medicine General, Child, Polyendocrinopathies, Autoimmune, Mice, Knockout, MESH: Middle Aged, Gastroenterology General, Gastroenterology, Inflammatory Disease, AIRE Protein, Genetics General, Middle Aged, [SDV] Life Sciences [q-bio], MESH: Transcription Factors / immunology, Pediatrics General, Female, Rheumatology General, Childhood Diseases, MESH: Interferon-gamma / immunology, Adult, MESH: T-Lymphocytes / immunology, MESH: Chemokine CXCL9 / genetics, MESH: Pyrazoles / therapeutic use, Adolescent, Knockout, Thyroid Disease, MESH: Autoantibodies / immunology, 610, T-Cells, Dermatology, MESH: Transcription Factors / genetics, Autoimmune Disease, Dermatology General, MESH: Polyendocrinopathies, Allergy/Immunology General, Allergy/Immunology, MESH: AIRE Protein / deficiency, Interferon-gamma, Adolescent Medicine, Rheumatology, Autoimmune / genetics, Outpatient-Based Clinical Medicine, 616, Nitriles, Genetics, Animals, Humans, Janus Kinase Inhibitors, Adrenal Disease, MESH: Mice, MESH: Autoantibodies / blood, MESH: Nitriles / therapeutic use, Autoantibodies, MESH: Adolescent, MESH: Humans, Animal, Inflammatory Bowel Disease, Immunity, Autoimmune / immunology, MESH: Adult, Endocrinology General, MESH: Pilot Projects, MESH: Male, Disease Models, Animal, Pyrimidines, Polyendocrinopathies, Disease Models, Autoimmune / drug therapy, Pyrazoles, MESH: Disease Models, Clinical Medicine, MESH: Female, Autoimmune, Transcription Factors
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 18 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 10% | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
| views | 14 | |
| downloads | 5 |

Views provided by UsageCounts
Downloads provided by UsageCounts