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b) detecting an elevated level of the lung autoantigen-reactive autoantibodies in said biological sample as compared to a control biological sample thereby determining the patient has ILD or a predisposition to ILD."],"number":1,"annotation":false,"title":false,"claim":true},{"lines":["The method of claim 1, wherein the lung autoantigen is a long palate, lung, and nasal epithelium carcinoma-associated protein 1 (LPLUNC 1)."],"number":2,"annotation":false,"title":false,"claim":true},{"lines":["The method of claim 1, wherein the lung autoantigen is a LPLUNC1-like protein comprising the amino acid sequence at least 70% identical to SEQ ID NO:2."],"number":3,"annotation":false,"title":false,"claim":true},{"lines":["The method of claim 1, wherein the biological sample is selected from a group consisting of blood, plasma, serum, bronchial alveolar lavage (BAL) fluid, and lung tissue."],"number":4,"annotation":false,"title":false,"claim":true},{"lines":["The method of claim 1, wherein the patient has or is suspected of having a systemic autoimmune disease."],"number":5,"annotation":false,"title":false,"claim":true},{"lines":["The method of claim 5, wherein the systemic autoimmune disease is selected from the group consisting of rheumatoid arthritis, scleroderma, Sjogren's syndrome, systemic lupus erythematosis, sarcoidosis, Wegener's granulomatosis, and autoimmune polyendocrine syndrome type 1 (APS-1)."],"number":6,"annotation":false,"title":false,"claim":true},{"lines":["The method of claim 1, wherein the antibody-based assay is selected from the group consisting of ELISA, Western blotting, immunofluorescence analysis, flow cytometry, and antibody microarray."],"number":7,"annotation":false,"title":false,"claim":true},{"lines":["The method of claim 7, wherein said antibody-based assay comprises a first reagent that specifically binds to said lung autoantigen-reactive autoantibodies, and a second reagent for detecting said autoantibodies, wherein said first reagent is the lung autoantigen or a cell expressing the lung autoantigen, and said second reagent comprises a secondary antibody that is reactive with constant regions of the autoantibodies."],"number":8,"annotation":false,"title":false,"claim":true},{"lines":["The method of claim 1, further comprising performing one or both of a pulmonary function test and a high resolution computed tomography scan on said patient."],"number":9,"annotation":false,"title":false,"claim":true},{"lines":["The method of claim 1, further comprising: c) administering a treatment to the patient when the elevated level of the lung autoantigen-reactive autoantibodies is detected."],"number":10,"annotation":false,"title":false,"claim":true},{"lines":["The method of claim 10, wherein said treatment is selected from the group consisting of a corticosteroid, cyclophosphamide, mycophenolate mofetil, and azathioprine."],"number":11,"annotation":false,"title":false,"claim":true},{"lines":["The method of claim 10, wherein said 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wherein the formulation comprises an effective amount of the lung autoantigen, or a peptide derived therefrom, wherein the autoantigen or the peptide is coupled to ethylene carbodiimide-fixed, autologous antigen presenting cells."],"number":14,"annotation":false,"title":false,"claim":true},{"lines":["The method of claim 10, wherein said treatment comprises a regulatory T cell regimen comprising dispensing a formulation to the patient by intravenous injection, wherein the formulation comprises an effective amount of ex vivo-expanded lung autoantigen-specific regulatory T 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