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8 results for “autoantibody signature”

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dryad36/100

Cystic fibrosis autoantibody signatures associate with Staphylococcus aureus lung infection or cystic fibrosis-related diabetes

<p>While cystic fibrosis (CF) lung disease is characterized by persistent inflammation and infections, and chronic inflammatory diseases are often accompanied by autoimmunity, autooimmune reactivity in CF has not been studied in depth. In this work, we undertook an unbiased approach to explore the systemic autoantibody repertoire in CF. Our results show higher levels of several new autoantibodies in the blood of people with CF (PwCF) compared to control subjects. Some of these are IgA autoantibodies targeting neutrophil components or autoantigens linked to neutrophil-mediated tissue damage in CF. We also found that PwCF with higher systemic IgM autoantibody levels have lower prevalence of <em>S. aureus</em> infection. On the other hand, IgM autoantibody levels in <em>S. aureus</em>-infected PwCF correlate with lung disease severity. Diabetic PwCF have significantly higher levels of IgA autoantibodies in their circulation compared to nondiabetic PwCF, and several of their IgM autoantibodies are associated with worse lung disease. In contrast, in nondiabetic PwCF blood levels of IgA autoantibodies correlate with lung disease. We have also identified other autoantibodies in CF that are associated with <em>P. aeruginosa</em> airway infection. In summary, we have identified several new autoantibodies and associations of autoantibody signatures with specific clinical features in CF.</p>

opencc-zeroAug 2023View details →
dryad36/100

Cystic fibrosis autoantibody signatures associate with Staphylococcus aureus lung infection or cystic fibrosis-related diabetes

Open the record for dataset details and reuse information.

publicAug 2023View details →
geo24/100

Whole genome-derived tiled peptide arrays detect pre-diagnostic autoantibody signatures in non-small cell lung cancer

GEO Series GSE128077. Homo sapiens. 174 samples. Type: Protein profiling by protein array.

openGEO-OpenMar 2019View details →
geo24/100

Combination of autoantibody signature with PSA level enables a highly accurate blood-based differentiation of prostate cancer patients from patients with benign prostatic hyperplasia

GEO Series GSE67068. Homo sapiens. 147 samples. Type: Protein profiling by protein array.

openGEO-OpenFeb 2017View details →
geo24/100

Discovery of tissue-specific proteomic signatures in juvenile dermatomyositis highlights pathways reflecting persistent disease activity, clinical heterogeneity, and myositis-specific autoantibody sub

GEO Series GSE308711. Homo sapiens. 88 samples. Type: Other.

openGEO-OpenSep 2025View details →
ClinicalTrials.gov24/100

Anti-IMP3 Autoantibody and MicroRNA Signature Blood Tests in Finding Metastasis in Patients With Localized or Metastatic Kidney Cancer

ClinicalTrials.gov study NCT00806650. IPD Sharing: Not stated. Countries: 1. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
zenodo16/100

Autoantibody Signature in Cardiac Arrest

<p><strong>Background:</strong> Cardiac arrest is a tragic event that causes one death roughly every 90 seconds</p> <p>worldwide. Survivors generally undergo a work-up to identify the etiology of arrest. However, 5-</p> <p>10% of cardiac arrest remain unexplained. As cardiac arrhythmias mostly underlie cardiac arrest</p> <p>and increasing evidence strongly supports the involvement of autoantibodies in</p> <p>arrhythmogenesis, a large-panel autoantibody screening was performed in cardiac arrest patients.</p> <p><strong>Methods:</strong> This is an observational, cross-sectional study of patients from the Montreal Heart</p> <p>Institute (MHI) hospital cohort, a single center registry of participants. A peptide microarray was</p> <p>designed to screen for IgG targeting epitopes from all known cardiac ion channels with</p> <p>extracellular domains. Plasma samples from 23 patients with unexplained cardiac arrest were</p> <p>compared to 22 cardiac arrest cases of ischemic origin and a group of 29 age-, sex- and BMImatched</p> <p>healthy subjects. The false discovery rate (FDR), LASSO logistic regression and</p> <p>random forest methods were jointly carried out to find significant differential IgG responses.</p> <p><strong>Results: </strong>The autoantibody against the pore domain of the L-type voltage-gated calcium channel</p> <p>(Cav1.2) was consistently identified as a biomarker of idiopathic cardiac arrest (P=0.002,</p> <p>FDR=0.007, classification accuracies &ge;0.83). Functional studies on human induced pluripotent</p> <p>stem cell-derived cardiomyocytes demonstrated that the anti-Cav1.2 IgG purified from patients</p> <p>with idiopathic cardiac arrest is proarrhythmogenic by reducing the action potential duration</p> <p>through calcium channel inhibition.</p> <p><strong>Conclusions: </strong>The present report addresses the concept of autoimmunity and cardiac arrest.</p> <p>Hitherto unknown autoantibodies targeting extracellular sequences of cardiac ion channels were</p> <p>detected. Moreover, the study identified an autoantibody signature specific to patients with</p> <p>cardiac arrest.</p>

restrictedApr 2020View details →
geo12/100

Evaluation of autoantibody signatures in meningioma patients using human proteome array

GEO Series GSE83507. Homo sapiens. 30 samples. Type: Protein profiling by protein array.

openGEO-OpenJun 2016View details →

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International Brain Laboratory public data

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Last verified 2026-04-29Open record