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European Respiratory Journal, ISSN 0903-1936, 10/2015, Volume 46, Issue 4, pp. 976 - 987
Journal Article
Chest, ISSN 0012-3692, 07/2017, Volume 152, Issue 1, pp. 103 - 112
Background Some patients with autoimmune characteristics and idiopathic interstitial pneumonia, particularly usual interstitial pneumonia (UIP), do not fit... 
interstitial pneumonia with autoimmune features | idiopathic pulmonary fibrosis | interstitial lung disease | autoimmune interstitial lung disease | CRITERIA | DIAGNOSIS | SCLERODERMA LUNG | PROGNOSIS | HEALTHY ELDERLY POPULATION | CONNECTIVE-TISSUE DISEASE | PREVALENCE | AUTOIMMUNE FEATURES | RESPIRATORY SYSTEM | LUNG-DISEASE | PULMONARY-FIBROSIS | CRITICAL CARE MEDICINE | Follow-Up Studies | Autoantibodies - blood | Humans | Middle Aged | Idiopathic Interstitial Pneumonias - diagnosis | Tomography, X-Ray Computed - methods | Male | Lung - diagnostic imaging | Statistics as Topic | Washington - epidemiology | Lung Diseases, Interstitial - diagnosis | Autoimmunity - immunology | Idiopathic Interstitial Pneumonias - physiopathology | Female | Lung Diseases, Interstitial - physiopathology | Needs Assessment | Connective Tissue Diseases - physiopathology | Diagnosis, Differential | Respiratory Function Tests - methods | Connective Tissue Diseases - diagnosis | Lung - physiopathology | Idiopathic Pulmonary Fibrosis - immunology | Idiopathic Interstitial Pneumonias - epidemiology | Lung Diseases, Interstitial - immunology | Idiopathic Pulmonary Fibrosis - diagnosis | Aged | Idiopathic Pulmonary Fibrosis - physiopathology | Cohort Studies | Idiopathic Interstitial Pneumonias - immunology | Autoantibodies | Pulmonary fibrosis | Health aspects | Analysis | Patient outcomes | Risk factors | UIP, usual interstitial pneumonia | IP, interstitial pneumonia | ILD, interstitial lung disease | UWMC, University of Washington Medical Center | PFT, pulmonary function test | CILD, Center for Interstitial Lung Diseases | AI-ILD, autoimmune interstitial lung disease | CTD, connective tissue disease | IPF, idiopathic pulmonary fibrosis | CTD-ILD, connective tissue disease-associated interstitial lung disease | NSIP, nonspecific interstitial pneumonia | IPAF, interstitial pneumonia with autoimmune features | Lone-IPF, IPF with negative CTD serologies | Dlco, diffusion capacity | Diffuse Lung Disease
Journal Article
PLoS ONE, ISSN 1932-6203, 04/2013, Volume 8, Issue 4, p. e60442
Objective: To identify similarities and differences in the clinical features of adult Japanese patients with individual anti-aminoacyl-tRNA synthetase... 
INTERSTITIAL LUNG-DISEASE | AMYOPATHIC DERMATOMYOSITIS | MYOSITIS-SPECIFIC AUTOANTIBODIES | ANTISYNTHETASE SYNDROME | POLYMYOSITIS | MULTIDISCIPLINARY SCIENCES | MUSCLE DISEASE | IDIOPATHIC INFLAMMATORY MYOPATHIES | CLASSIFICATION | JAPANESE PATIENTS | SYSTEMIC-SCLEROSIS | Amino Acyl-tRNA Synthetases - immunology | Scleroderma, Systemic - blood | Prevalence | Dermatomyositis - blood | Autoantibodies - blood | Humans | Middle Aged | Male | Lupus Erythematosus, Systemic - blood | Adrenal Cortex Hormones - therapeutic use | Young Adult | Polymyositis - epidemiology | Dermatomyositis - immunology | Lung Diseases, Interstitial - blood | Dermatomyositis - drug therapy | Lupus Erythematosus, Systemic - immunology | Adult | Female | Lung Diseases, Interstitial - epidemiology | Polymyositis - immunology | Polymyositis - drug therapy | Lupus Erythematosus, Systemic - epidemiology | Dermatomyositis - epidemiology | Scleroderma, Systemic - immunology | Scleroderma, Systemic - epidemiology | Syndrome | Lung Diseases, Interstitial - immunology | Polymyositis - blood | Adolescent | Aged | Viral antibodies | Antibodies | Lung diseases, Interstitial | Analysis | Transfer RNA | Immunoglobulins | Immunoprecipitation | tRNA | Internal medicine | Dermatology | Pathogenesis | Exanthema | Lung diseases | Rheumatology | Dermatomyositis | Science | Arthritis | Medical diagnosis | Patients | Medicine | Medical centres | Polymyositis | Hospitals | Myositis | Skin | Aminoacyl-tRNA ligase | University graduates
Journal Article
Nature Medicine, ISSN 1078-8956, 12/2014, Volume 20, Issue 12, pp. 1410 - 1416
The protein cytotoxic T lymphocyte antigen-4 (CTLA-4) is an essential negative regulator of immune responses, and its loss causes fatal autoimmunity in mice.... 
PATHWAYS | MEDICINE, RESEARCH & EXPERIMENTAL | CLINICAL-PICTURE | HOMEOSTASIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | CELL BIOLOGY | AUTOIMMUNITY | REGULATORY T-CELLS | GERMLINE MUTATIONS | MICE | BLOCKADE | IMMUNODEFICIENCY | ABATACEPT | Recurrence | Agammaglobulinemia - immunology | Agammaglobulinemia - genetics | Purpura, Thrombocytopenic, Idiopathic - genetics | Exons | Immune System Diseases - genetics | Humans | Middle Aged | Male | Anemia, Hemolytic, Autoimmune - genetics | Mutation, Missense | Respiratory Tract Infections - genetics | T-Lymphocytes, Regulatory - immunology | Autoimmune Diseases - genetics | Young Adult | Purpura, Thrombocytopenic, Idiopathic - immunology | Adult | Female | Endocytosis - genetics | Polyendocrinopathies, Autoimmune - genetics | Child | Endocytosis - immunology | Granuloma - genetics | Autoimmune Diseases - immunology | CTLA-4 Antigen - genetics | B7-1 Antigen - metabolism | Codon, Nonsense | CTLA-4 Antigen - immunology | Syndrome | Polyendocrinopathies, Autoimmune - immunology | Lung Diseases, Interstitial - immunology | Animals | B-Lymphocytes - immunology | Lung Diseases, Interstitial - genetics | Pedigree | Anemia, Hemolytic, Autoimmune - immunology | Adolescent | Respiratory Tract Infections - immunology | Granuloma - immunology | Heterozygote | Mice | Antigens | Gene mutations | Physiological aspects | Genetic aspects | Immunologic diseases | Research | Risk factors | Proteins | Homeostasis | Cytotoxicity | Ligands | T cell receptors | Mutation | Immune system
Journal Article
Journal Article
Clinics in Chest Medicine, ISSN 0272-5231, 09/2016, Volume 37, Issue 3, pp. 463 - 474
Journal Article
Journal Article
Journal Article
Journal Article
Journal of Clinical Immunology, ISSN 0271-9142, 1/2013, Volume 33, Issue 1, pp. 30 - 39
A subset of patients with common variable immunodeficiency (CVID) develops granulomatous and lymphocytic interstitial lung disease (GLILD), a restrictive lung... 
Medical Microbiology | Biomedicine | Immunology | Common variable immunodeficiency (CVID) | primary immunodeficiency | Infectious Diseases | Internal Medicine | azathioprine | lung disease | rituximab | granulomatous and lymphocytic interstitial lung disease (GLILD) | Rituximab | Lung disease | Azathioprine | Granulomatous and lymphocytic interstitial lung disease (GLILD) | Primary immunodeficiency | STANDARDIZATION | IMMUNE-DEFICIENCY | IMMUNOLOGY | CANCER | REFERENCE VALUES | B-CELL | LYMPHOMA | MANIFESTATIONS | T-Lymphocyte Subsets - immunology | Common Variable Immunodeficiency - immunology | Azathioprine - administration & dosage | Common Variable Immunodeficiency - drug therapy | Lung Diseases, Interstitial - pathology | Humans | Antibodies, Monoclonal, Murine-Derived - administration & dosage | Male | Young Adult | T-Lymphocyte Subsets - drug effects | Adult | B-Lymphocyte Subsets - immunology | Female | Retrospective Studies | Drug Therapy, Combination | B-Lymphocyte Subsets - drug effects | B-Lymphocyte Subsets - pathology | Administration, Oral | Common Variable Immunodeficiency - pathology | Lung Diseases, Interstitial - drug therapy | Granuloma - pathology | Lung Diseases, Interstitial - immunology | T-Lymphocyte Subsets - pathology | Adolescent | Granuloma - drug therapy | Granuloma - immunology | Infusions, Intravenous | Medical colleges | Complications and side effects | Usage | Care and treatment | Chemotherapy | Mortality | Lung diseases | Immunological deficiency syndromes | Drug therapy, Combination | Cancer
Journal Article
Laboratory Investigation, ISSN 0023-6837, 06/2010, Volume 90, Issue 6, pp. 812 - 823
Journal Article