Search results for "autoantibodie"

showing 10 items of 294 documents

Association of Thyroid Function Test Abnormalities and Thyroid Autoimmunity With Preterm Birth A Systematic Review and Meta-analysis

2019

Preterm birth complicates 5% to 15% of births worldwide, and although it is the most important direct cause of morbidity and mortality in children younger than 5 years, no known risk factors can be identified in the majority of cases. However, overt hypothyroidism and hyperthyroidism during pregnancy are well-known risk factors for preterm birth, and as such, the purpose of this study was to assess whether thyroid function test abnormalities and thyroid peroxidase (TPO) antibody positivity were associated with preterm birth. The study conducted a systematic review on the association of thyroid function or autoimmunity with preterm birth published from database inception to March 18, 2018, w…

Thyrotropin/bloodIodide Peroxidase/immunologyPremature Birth/etiologyThyrotropinHypothyroidism/complicationsThyroid Function Tests01 natural sciencesThyroxine/blood0302 clinical medicineMaternal hypothyroidismThyroid Diseases/bloodPregnancyEuthyroid030212 general & internal medicine030219 obstetrics & reproductive medicinebiologymedicine.diagnostic_testObstetricsThyroid diseaseAbsolute risk reductionObstetrics and GynecologyGestational ageGeneral MedicinePremature birthPremature BirthFemaleThyroid functionmedicine.drugAdultendocrine systemmedicine.medical_specialtyLevothyroxineGestational AgeIodide PeroxidaseThyroid function testsAutoimmune Diseases03 medical and health sciencesHypothyroidismThyroid peroxidasemedicineVery Preterm BirthHumans0101 mathematicsAutoantibodiesPregnancybusiness.industry010102 general mathematicsInfant NewbornInfantOdds ratioNewbornmedicine.diseaseThyroid DiseasesPregnancy Complications/bloodPregnancy ComplicationsThyroxineAutoimmune Diseases/bloodbiology.proteinAutoantibodies/bloodbusiness
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Analysis of complex autoantibody repertoires by surface-enhanced laser desorption/ionization-time of flight mass spectrometry

2003

Normal sera contain a large number of naturally occurring autoantibodies which can mask important disease-associated ones. Western blotting has evolved as the most important tool to demonstrate autoantibodies in autoimmune diseases, because of its ability to simultaneous screening for a wide spectrum of different antigens. In previous studies we have shown the diagnostic potential of the analysis of autoantibodies in autoimmune diseases by means of multivariate statistics and artificial neural networks. However, the Western blotting procedure remains very time-consuming and is also limited in sensitivity. Therefore, we used an on-chip approach for the analysis of autoantibodies. This Protei…

Time FactorsChromatographymedicine.diagnostic_testMolecular massmedicine.drug_classChemistryBlotting WesternProtein Array AnalysisAutoantibodyMass spectrometryMonoclonal antibodySensitivity and SpecificityBiochemistryMass SpectrometrySurface-enhanced laser desorption/ionizationMolecular WeightBlotWestern blotSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationmedicineHumansTime-of-flight mass spectrometryMolecular BiologyAutoantibodiesPROTEOMICS
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Anti‐laminin auto antibodies in ANCA‐associated vasculitis

2000

Background. Endothelial cell damage occurs during vasculitic processes in vivo. With the alteration of the endothelium, exposure to basement membrane components may occur with induction of humoral immunity. Methods. In the present study, we evaluated the prevalence of antibodies against the basement membrane antigen laminin (LMN) in patients with ANCA-associated systemic vasculitis (AASV), pathologic controls (systemic lupus erythematosus, mixed cryoglobulinaemia, Henoch Schonlein purpura, primary glomerulonephritis) and normal individuals. Results. By ELISA, 21.6% of AASV (16/74) and 10% of pathologic controls (3/30), but only one of the normal controls (2.8%) had these antibodies (P = 0.0…

VasculitisPathologymedicine.medical_specialtyHenoch-Schonlein purpuraMyeloblastinEnzyme-Linked Immunosorbent AssayAntibodies Antineutrophil CytoplasmicEpitopesAntigenReference Valuesimmune system diseasesmedicineHumansReference Valuecardiovascular diseasesAutoantibodiesPeroxidaseAnti-neutrophil cytoplasmic antibodyTransplantationbusiness.industrySerine EndopeptidasesGranulomatosis with PolyangiitisGlomerulonephritismedicine.diseaseAutoantibodieSerine EndopeptidaseNephrologyImmunologyEpitopeLamininGranulomatosis with PolyangiitiGranulomatosis with polyangiitisVasculitisbusinessMicroscopic polyangiitisHumanSystemic vasculitisNephrology Dialysis Transplantation
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Detection of anti-myeloperoxidase antibodies in the serum of patients with type 1 diabetes mellitus.

1996

Anti-myeloperoxidase (anti-MPO) antibodies were detected in 34 of 88 (38%) patients with type 1 diabetes mellitus but in only 3 of 55 (5.7%) healthy subjects and in 4 of 20 patients with autoimmune disease. Specificity of anti-MPO antibodies was assessed by MPO inhibition studies. No relationship was found between the occurrence of anti-MPO and anti-thyroperoxidase antibodies. Levels of soluble intercellular adhesion molecule 1 (ICAM-1) were found to be higher in anti-MPO antibody-positive (n = 28, 508 +/- 126 ng/ml) than in anti-MPO antibody-negative (n = 58, 438 +/- 140 ng/ml: P < 0.05) patients. A state of chronic neutrophil activation has been described in diabetes mellitus. As anti-MPO…

Vasculitismedicine.medical_specialtyAdolescentmedicine.drug_classEndocrinology Diabetes and MetabolismDiabetic angiopathyMonoclonal antibodyIodide PeroxidaseAntibodies Antineutrophil CytoplasmicEndocrinologyDiabetes mellitusInternal medicineInternal MedicineMedicineHumansChildFluorescent Antibody Technique IndirectAutoantibodiesPeroxidaseAutoimmune diseaseType 1 diabetesbiologybusiness.industryGeneral Medicinemedicine.diseaseIntercellular Adhesion Molecule-1EndocrinologyDiabetes Mellitus Type 1MyeloperoxidaseChild PreschoolImmunoglobulin Gbiology.proteinAntibodybusinessSystemic vasculitisActa diabetologica
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Moving from Dermatomyositis Associated with Anti-Melanoma Differentiation-Associated Gene 5 Antibody to Anti-Melanoma Differentiation-Associated Gene…

2018

International audience

[SDV.MHEP.RSOA] Life Sciences [q-bio]/Human health and pathology/Rhumatology and musculoskeletal systemMyositis[SDV.MHEP.RSOA]Life Sciences [q-bio]/Human health and pathology/Rhumatology and musculoskeletal systemMyopathyInterstitial lung diseaseComputingMilieux_MISCELLANEOUSDermatomyositisAutoantibodies
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Autoantibody production in aging: effect of cytokine gene polymorphisms in Sicilian ultra-nonagenarians

2012

aging autoantibodies ultra-nonagenariansSettore MED/05 - Patologia Clinica
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Chaperonopathies and chaperonotherapy. Hsp60 as therapeutic target in cancer: potential benefits and risks.

2013

In this minireview we focus on Hsp60 as a target for anticancer therapy. We discuss the new concepts of chaperonopathies and chaperonotherapy and present information on Hsp60 localization in the cell membrane of human tumor cells. We describe novel mechanisms for Hsp60 reaching the extracellular environment that involve membrane-associated stages, as well as data on anti-Hsp60 antibodies found in human sera, both in normal subjects and patients affected by autoimmune diseases. Finally, we discuss possible therapeutic applications of anti-Hsp60 antibodies in cancer treatment, evaluating also side effects on non-tumor cells. In conclusion, the way for investigating Hsp60-targeted anti-tumor t…

animal structuresCellchemical and pharmacologic phenomenaAntineoplastic AgentsBiologycomplex mixturesRisk AssessmentCell membraneDrug Delivery SystemsRisk FactorsNeoplasmsDrug DiscoverymedicineExtracellularAnimalsHumansSecretionPharmacologyMechanism (biology)fungiCancerChaperonin 60medicine.diseasemedicine.anatomical_structureImmunologybiology.proteinCancer researchHsp60 Cpn60 HSPD1 plasma membrane antibodies autoantibodies antitumor immunotherapy anticancer therapy chaperonopathies human sera.HSP60AntibodyCurrent pharmaceutical design
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A longitudinal study of C1q and anti-C1q autoantibodies in homologous and heterologous pregnancies for predicting pre-eclampsia

2022

C1q, the recognition molecule of the classical pathway of the complement system, plays a central role in pregnancy. Lack of C1q is characterized by poor trophoblast invasion and pregnancy failure. C1q can be the target of an antibody response: anti‐C1q autoantibodies (anti-C1q) are present in several infectious and autoimmune diseases. The presence of these autoantibodies has been detected also in 2-8% of the general population. Recent evidence indicates that women who undergo assisted reproductive technology (ART) have an increased risk of developing pre-eclampsia (PE), particularly oocyte donation (OD) pregnancies. The aim of this study was to characterize the levels of C1q and anti-C1q i…

anti-C1q autoantibodiepre-eclampsiaART pregnancy; C1q; anti-C1q autoantibodies; oocyte donation; pre-eclampsia; Female; Humans; Pregnancy; Autoantibodies; Complement C1q; Longitudinal Studies; Placenta; Pre-Eclampsiapre-eclampsia.Complement C1qPlacentaImmunologyanti-C1q autoantibodiesLongitudinal StudieART pregnancySettore MED/08 - Anatomia PatologicaAutoantibodiePre-EclampsiaPregnancyoocyte donationSettore MED/05 - Patologia ClinicaImmunology and AllergyHumansFemaleLongitudinal StudiesC1qAutoantibodiesHuman
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AUTOANTIBODIES IDENTIFICATION IN BREAST CANCER SERA BY PROTEOMIC APPROACH

2011

autoantibodies
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Immunogenic hotspots in the spacer domain of ADAMTS13 in immune‐mediated thrombotic thrombocytopenic purpura

2021

International audience; Background Immune-mediated thrombotic thrombocytopenic purpura (iTTP) is caused by anti-ADAMTS13 autoantibodies inducing a severe deficiency of ADAMTS13. Epitope mapping studies on samples obtained during acute iTTP episodes have shown that the iTTP immune response is polyclonal, with almost all patients having autoantibodies targeting the spacer domain of ADAMTS13.Objectives To identify the immunogenic hotspots in the spacer domain of ADAMTS13.Patients/methods A library of 11 full-length ADAMTS13 spacer hybrids was created in which amino acid regions of the spacer domain of ADAMTS13 were exchanged by the corresponding region of the spacer domain of ADAMTS1. Next, th…

autoantibodiesADAMTS13 Protein030204 cardiovascular system & hematologyEpitope03 medical and health sciencesEpitopes0302 clinical medicineVon Willebrand factorimmunophenotypinghemic and lymphatic diseasesHumansthrombotic thrombocytopenic purpurachemistry.chemical_classificationbiologyPurpura Thrombotic ThrombocytopenicAutoantibodyHematologyMolecular biologyADAMTS13ADAMTS133. Good healthAmino acidepitope mappingEpitope mappingchemistryPolyclonal antibodiesImmunoglobulin Gbiology.proteinDNA IntergenicAntibody[SDV.MHEP]Life Sciences [q-bio]/Human health and pathology
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