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1.

001-es BibID:BIBFORM069472
Első szerző:Kalliokoski, Suvi
Cím:Transglutaminase 2-specific coeliac disease autoantibodies induce morphological changes and signs of inflammation in the small-bowel mucosa of mice / Suvi Kalliokoski, Victoria Ortín Piqueras, Rafael Frías, Ana-Marija Sulic, Juha A. E. Määttä, Niklas Kähkönen, Keijo Viiri, Heini Huhtala, Arja Pasternack, Kaija Laurila, Daniele Sblattero, Ilma R. Korponay-Szabó, Markku Mäki, Sergio Caja, Katri Kaukinen, Katri Lindfors
Dátum:2017
ISSN:0939-4451 1438-2199
Tárgyszavak:Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
Megjelenés:Amino Acids 49 : 3 (2017), p. 529-540. -
További szerzők:Piqueras, Victoria Ortín Frías, Rafael Sulic, Ana-Marija Määttä, Juha A. E. Kähkönen, Niklas Viiri, Keijo Huhtala, Heini Pasternack, Arja Laurila, Kaija Sblattero, Daniele Korponay-Szabó Ilma (1959-) (gyermekgyógyász) Mäki, Markku Caja, Sergio Kaukinen, Katri Lindfors, Katri
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2.

001-es BibID:BIBFORM056541
Első szerző:Kalliokoski, Suvi
Cím:Injection of celiac disease patient sera or immunoglobulins to mice reproduces a condition mimicking early developing celiac disease / Suvi Kalliokoski, Sergio Caja, Rafael Frias, Kaija Laurila, Outi Koskinen, Onni Niemelä, Markku Mäki, Katri Kaukinen, Ilma R. Korponay-Szabó, Katri Lindfors
Dátum:2015
ISSN:0946-2716
Megjegyzések:Typical features of celiac disease are small-bowel villus atrophy, crypt hyperplasia, and inflammation which develop gradually concomitant with ingestion of gluten. In addition, patients have anti-transglutaminase 2 (TG2) autoantibodies in their serum and tissues. The aim of this study was to establish whether celiac disease can be passively transferred to mice by serum or immunoglobulins. Serum aliquots or purified immunoglobulins (Ig) were intraperitoneally injected into Hsd:Athymic Nude-Foxn1nu mice for 8 or 27 days. As mice do not have proper IgA transport from peritoneum to blood, sera with a high content of IgG class anti-TG2 antibodies from untreated IgA-deficient celiac patients were used. Mouse sera were tested for celiac disease-specific autoantibodies, and several tissues were analyzed for autoantibody deposits targeted to TG2. Morphological assessment was made of the murine small intestinal mucosa. Injection of celiac disease patient sera or total IgG led to a significant delay in weight gain and mild diarrhea in a subset of mice. The mice injected with celiac patient sera or IgG had significantly decreased villus height crypt depth (Vh/CrD) ratios and celiac diseasespecific autoantibody deposits targeted to TG2 in several tissues, including the small intestine. None of these features were observed in control mice. We conclude that administration of IgA-deficient celiac disease patient serum or total IgG induces both deterioration of the intestinal mucosa and clinical features of celiac disease in mice. The experimentally induced condition in the mice injected with patient serum or IgG resembles early developing celiac disease in humans.
Tárgyszavak:Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
Autoantibodies
Celiac disease
Passivetransfer
Transglutaminase 2
Megjelenés:Journal of Molecular Medicine-Jmm 93 : 1 (2015), p. 51-62. -
További szerzők:Caja, Sergio Frías, Rafael Laurila, Kaija Koskinen, Outi Niemelä, Onni Mäki, Markku Kaukinen, Katri Korponay-Szabó Ilma (1959-) (gyermekgyógyász) Lindfors, Katri
Pályázati támogatás:101788
OTKA
TÁMOP-4.2.2.A-11/1/KONV-2012-0023
TÁMOP
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3.

001-es BibID:BIBFORM086064
Első szerző:Korponay-Szabó Ilma (gyermekgyógyász)
Cím:Rapid detection of coeliac autoantibodies in the office / Korponay-Szabó I. R., Raivio T. M., Laurila K., Kovács J. B., Nemes É., Kaukinen K., Mäki M.
Dátum:2005
ISSN:0277-2116
Tárgyszavak:Orvostudományok Klinikai orvostudományok idézhető absztrakt
folyóiratcikk
Megjelenés:Journal of Pediatric Gastroenterology and Nutrition. - 40 : 5 (2005), p. 619. -
További szerzők:Raivio, Tiina Laurila, Kaija Kovács J. Béla Nemes Éva (1957-) (csecsemő- és gyermekgyógyász, gasztroenterológus) Kaukinen, Katri Mäki, Markku
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4.

001-es BibID:BIBFORM057472
Első szerző:Korponay-Szabó Ilma (gyermekgyógyász)
Cím:Transglutaminase expression and coeliac autoantibody binding to the pancreas in diabetes mellitus / I. R. Korponay-Szabo, M. Oikarinen, J. E. Laiho, K. Laurila, M. Maki, H. Hyoty, The nPOD Study Group
Dátum:2014
ISSN:2050-6406 2050-6414
Tárgyszavak:Orvostudományok Klinikai orvostudományok idézhető absztrakt
Megjelenés:United European Gastroenterology Journal. - 2 : Suppl. 1 (2014), p. A129. -
További szerzők:Oikarinen, M. Laiho, J. E. Laurila, Kaija Mäki, Markku Hyoty, H. The nPOD Study Group
Pályázati támogatás:TÁMOP-4.2.2.A-11/1/KONV-2012-0023
TÁMOP
K101788
OTKA
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Intézményi repozitóriumban (DEA) tárolt változat
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5.

001-es BibID:BIBFORM044303
Első szerző:Korponay-Szabó Ilma (gyermekgyógyász)
Cím:Elevation of IgG antibodies against tissue transglutaminase as a diagnostic tool for coeliac disease in selective IgA deficiency / Korponay-Szabó I. R., Dahlbom I., Laurila K., Koskinen S., Woolley N., Partanen J., B. Kovács J., Mäki M., Hansson T.
Dátum:2003
ISSN:0017-5749
Megjegyzések:BACKGROUND:IgA serum autoantibodies against tissue transglutaminase (tTG) have an established diagnostic value in coeliac disease, and high efficacy tests are widely available for their detection. However, serological evaluation of IgA deficient subjects is still difficult.AIMS:To evaluate the diagnostic potential of IgG class anti-tTG autoantibodies measured quantitatively using an enzyme linked immunosorbent assay (ELISA) compared with immunofluorescent detection of coeliac autoantibodies.PATIENTS:We tested serum samples from 325 IgA deficient subjects, including 78 patients with coeliac disease, 73 disease controls, and 174 blood donors.METHODS:IgG antibodies against human recombinant tTG were measured with an ELISA. IgG antiendomysium antibodies (EMA) were assayed by indirect immunofluorescence on human jejunum and appendix sections.RESULTS:The IgG anti-tTG ELISA had a sensitivity of 98.7% and a specificity of 98.6%, and the correlation with IgG EMA titres was high (r(s)=0.91). One coeliac patient, initially negative in all autoantibody tests, displayed both IgG anti-tTG antibodies and IgG EMA during later gluten exposure. IgG anti-tTG antibodies and EMA titres showed significant decreases (p<0.001) in treated patients. The frequency of IgG anti-tTG autoantibody positivity was 9.8% among IgA deficient blood donors and 11 of the 12 positive subjects with known HLA-DQ haplotypes carried DQ2 or DQ8 alleles.CONCLUSIONS:IgG anti-tTG and IgG EMA autoantibody tests are highly efficient in detecting coeliac disease in IgA deficient patients. The high prevalence of coeliac antibodies among symptom free IgA deficient blood donors who also carry coeliac-type HLA-DQ genes indicates that all IgA deficient persons should be evaluated for coeliac disease.
Tárgyszavak:Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
Megjelenés:Gut. - 52 : 11 (2003), p. 1567-1571. -
További szerzők:Dahlbom, Ingrid Laurila, Kaija Koskinen, Seppo Woolley, Nina Partanen, Jukka B. Kovács Judit Mäki, Markku Hansson, Tony
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6.

001-es BibID:BIBFORM044305
Első szerző:Korponay-Szabó Ilma (gyermekgyógyász)
Cím:Tissue Transglutaminase Is the Target in Both Rodent and Primate Tissues for Celiac Disease - Specific Autoantibodies / Korponay-Szabo Ilma R., Sulkanen Satu, Halttunen Tuula, Maurano Francesco, Rossi Mauro, Mazzarella Giuseppe, Laurila Kaija, Troncone Riccardo, Maki Markku
Dátum:2000
ISSN:0277-2116
Megjegyzések:BACKGROUND:Endomysial antibodies have recently been shown to react with tissue transglutaminase. This study was undertaken to investigate whether the tissue distribution of transglutaminase is also compatible with reticulin, jejunal, and fibroblast autoantibody binding patterns.METHODS:Sera from patients with and without celiac disease, monoclonal tissue transglutaminase antibodies, and sera from mice parenterally immunized against commercially available tissue transglutaminase, transglutaminase complexed with gliadin, or gliadin were used in indirect immunofluorescence and double-staining studies using both rodent and primate tissues as substrates. Also, antibody competition, affinity chromatography, and potassium thiocyanate extraction studies were undertaken.RESULTS:Tissue transglutaminase antibody binding patterns were identical with the extracellular binding patterns seen with celiac patient sera. Human umbilical cord-derived fibroblasts exhibited both cytoplasmic and extracellular matrix staining. Double staining with patients' sera and tissue transglutaminase antibodies showed complete overlapping. Tissue transglutaminase effectively absorbed reticulin-endomysial antibodies from celiac sera, and patients' sera blocked the staining of the monoclonal tissue transglutaminase antibodies. Potassium thiocyanate extraction abolished the staining patterns, but they were elicited again after readdition of tissue transglutaminase.CONCLUSIONS:Reticulin, endomysial, and jejunal antibodies detect transglutaminase in both rodent and primate tissues, indicating that these tissue autoantibodies are identical
Tárgyszavak:Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
Megjelenés:Journal Of Pediatric Gastroenterology And Nutrition. - 31 : 5 (2000), p. 520-527. -
További szerzők:Sulkanen, Satu Halttunen, Tuula Maurano, Francesco Rossi, Mauro Mazzarella, Giuseppe Laurila, Kaija Troncone, Riccardo Mäki, Markku
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7.

001-es BibID:BIBFORM042704
035-os BibID:PMID:16197494
Első szerző:Korponay-Szabó Ilma (gyermekgyógyász)
Cím:Coeliac disease case finding and diet monitoring by point-of-care testing / I. R. Korponay-Szabó, T. Raivio, K. Laurila, J. Opre, R. Király, J. B. Kovács, K. Kaukinen, L. Fésüs, M. Mäki
Dátum:2005
ISSN:0269-2813
Megjegyzések:BACKGROUND: Immunoglobulin A class transglutaminase autoantibodies are highly predictive markers of active coeliac disease, a disorder difficult to recognize solely on clinical grounds. AIMS: To develop and evaluate a simple rapid test for point-of-care detection of coeliac autoantibodies. METHODS: The novel whole blood test utilizes the patient's endogenous transglutaminase in red blood cells for detection of transglutaminase-specific immunoglobulin A antibodies present in the blood sample, with normal plasma immunoglobulin A detection as positive test control. We evaluated 284 patients under suspicion of coeliac disease and undergoing jejunal biopsy, and 263 coeliac patients on a gluten-free diet, 383 being tested prospectively in a point-of-care setting. Results were compared with histology, conventional serum autoantibody results and dietary adherence. RESULTS: The rapid test showed 97% sensitivity and 97% specificity for untreated coeliac disease, and identified all immunoglobulin A-deficient samples. Point-of-care testing found new coeliac cases as efficiently as antibody tests in laboratory. Coeliac autoantibodies were detected onsite in 21% of treated patients, while endomysial and transglutaminase antibodies were positive in 20% and 19%, respectively. The positivity rate correlated with dietary lapses and decreased on intensified dietary advice given upon positive point-of-care test results. CONCLUSIONS: Point-of-care testing was accurate in finding new coeliac cases and helped to identify and decrease dietary non-compliance.
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
egyetemen (Magyarországon) készült közlemény
Megjelenés:Alimentary Pharmacology and Therapeutics. - 22 : 8 (2005), p. 729-737. -
További szerzők:Raivio, Tiina Laurila, Kaija Opre Judit (Kenézy Gyula Kórház) Király Róbert (1975-) (biológus) Kovács J. Béla Kaukinen, Katri Fésüs László (1947-) (orvos biokémikus) Mäki, Markku
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8.

001-es BibID:BIBFORM042703
035-os BibID:PMID:15082580
Első szerző:Korponay-Szabó Ilma (gyermekgyógyász)
Cím:In vivo targeting of intestinal and extraintestinal transglutaminase 2 by coeliac autoantibodies / I. R. Korponay-Szabo, T. Halttunen, Z. Szalai, K. Laurila, R. Király, J. B. Kovács, L. Fésüs, M. Mäki
Dátum:2004
ISSN:0017-5749
Megjegyzések:BACKGROUND: IgA class serum autoantibodies against type 2 (tissue) transglutaminase (TG2) bind to both intestinal and extraintestinal normal tissue sections in vitro, eliciting endomysial, reticulin, and jejunal antibody reactions. It is not known whether similar binding also occurs in coeliac patients in vivo, and may thereby contribute to disease manifestations. AIMS: To investigate intestinal and extraintestinal coeliac tissues for the presence of in vivo bound TG2 specific IgA and its relation to small intestinal mucosal atrophy. PATIENTS: We investigated jejunal samples with normal villous morphology from 10 patients with developing coeliac disease who subsequently progressed to a flat lesion, from 11 patients with dermatitis herpetiformis, and from 12 non-coeliac controls. Six extrajejunal biopsy samples (liver, lymph node, muscle, appendix), obtained based on independent clinical indications from patients with active coeliac disease, were also studied. METHODS: Double colour immunofluorescent studies for in situ IgA, TG2, and laminin were performed. IgA was eluted from tissue sections and tested for TG2 specificity by enzyme linked immunosorbent assay and indirect immunofluorescence. RESULTS: IgA (in one IgA deficient case IgG) deposition on extracellularly located TG2 was detected in jejunal and extrajejunal specimens of all coeliac patients, and also in seven of 11 dermatitis herpetiformis patients, of whom two had no circulating endomysial antibodies. IgA eluted from extraintestinal coeliac tissues was targeted against TG2. CONCLUSIONS: Coeliac IgA targets jejunal TG2 early in disease development even when endomysial antibodies are not present in the circulation. Extraintestinal target sites of coeliac IgA further indicate that humoral immunity may have a pathogenetic role.
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
egyetemen (Magyarországon) készült közlemény
Megjelenés:Gut. - 53 : 5 (2004), p. 641-648. -
További szerzők:Halttunen, Tuula Szalai Zoltán Laurila, Kaija Király Róbert (1975-) (biológus) Kovács J. Béla Fésüs László (1947-) (orvos biokémikus) Mäki, Markku
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9.

001-es BibID:BIBFORM028773
Első szerző:Korponay-Szabó Ilma (gyermekgyógyász)
Cím:Missing endomysial and reticulin binding of coeliac antibodies in transglutaminase 2 knockout tissues / I. R. Korponay-Szabó, K. Laurila, Zs. Szondy, T. Halttunen, Z. Szalai, I. Dahlbom, I. Rantala, J. B. Kovács, L. Fésüs, M. Mäki
Dátum:2003
ISSN:0017-5749
Megjegyzések:Autoantibodies against transglutaminase 2 (TG2) are thought to be responsible for the endomysial (EMA), reticulin (ARA), and jejunal antibody (JEA) tissue binding of serum samples from coeliac patients but the exclusive role of TG2 in these staining patterns has not yet been established. AIMS: To evaluate whether antigens other than TG2 contribute to EMA/ARA/JEA reactions. PATIENTS: Serum samples from 61 EMA/ARA/JEA positive untreated patients with coeliac disease, 40 dermatitis herpetiformis patients, and 34 EMA/ARA/JEA negative non-coeliac controls were tested. METHODS: TG2 knockout (TG2-/-) and wild-type mouse oesophagus, jejunum, liver, and kidney sections, and TG2-/- sections coated with human recombinant TG2 were used as substrates in single and double immunofluorescent studies for patient IgA binding and tissue localisation of TG2, fibronectin, actin, and calreticulin. RESULTS: None of the patient serum samples elicited EMA, ARA, or JEA binding in TG2-/- morphologically normal tissues. In contrast, 96 of 101 gluten sensitive patient samples (95%) reacted with wild-type mouse tissues and all 101 reacted in EMA/ARA/JEA patterns with TG2-/- mouse tissues coated with human TG2. Serum IgA binding to TG2-/- smooth muscle cells was observed in low titres in 31.1%, 27.5%, and 20.5%, and to TG2-/- epithelium in 26.3%, 5.0%, and 8.8% of coeliac, dermatitis herpetiformis, and control samples, respectively. These positivities partly colocalised with actin and calreticulin but not with TG2 or fibronectin. CONCLUSIONS: EMA/ARA/JEA antibody binding patterns are exclusively TG2 dependent both in coeliac and dermatitis herpetiformis patients. Actin antibodies are responsible for some positivities which are not part of the EMA/ARA/JEA reactions.
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
egyetemen (Magyarországon) készült közlemény
Megjelenés:Gut 52 : 2 (2003), p. 199-204. -
További szerzők:Laurila, Kaija Szondy Zsuzsanna (1959-) (molekuláris sejtbiológus, biokémikus) Halttunen, Tuula Szalai Zoltán Dahlbom, Ingrid Rantala, I. Kovács B. J. Fésüs László (1947-) (orvos biokémikus) Mäki, Markku
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10.

001-es BibID:BIBFORM096519
035-os BibID:(cikkazonosító)1594 (WoS)000662368300001 (Scopus)85105759721
Első szerző:Nurmi, Rakel
Cím:Celiac Disease-Type Tissue Transglutaminase Autoantibody Deposits in Kidney Biopsies of Patients with IgA Nephropathy / Nurmi Rakel, Korponay-Szabó Ilma, Laurila Kaija, Huhtala Heini, Niemelä Onni, Mustonen Jukka, Mäkelä Satu, Kaukinen Katri, Lindfors Katri
Dátum:2021
ISSN:2072-6643
Megjegyzések:An association between celiac disease and IgA nephropathy (IgAN) has been suggested. In celiac disease, in addition to circulating in serum, IgA-class tissue transglutaminase (tTG) autoantibodies are deposited in the small bowel mucosa and extraintestinal organs. In this case series of IgAN patients with or without celiac disease, we studied whether celiac disease-type IgA-tTG deposits occur in kidney biopsies. The study included nine IgAN patients, four of them with celiac disease. At the time of the diagnostic kidney biopsy serum tTG autoantibodies were measured and colocalization of IgA and tTG was investigated in the frozen kidney biopsies. Three IgAN patients with celiac disease had IgA-tTG deposits in the kidney even though in two of these the celiac disease diagnosis had been set years later. These deposits were not found in a patient with already diagnosed celiac disease following a gluten-free diet. Of the five non-celiac IgAN patients, three had IgA-tTG deposits in the kidney. We conclude that tTG-targeted IgA deposits can be found in the kidney biopsies of gluten-consuming IgAN patients but their specificity to celiac disease seems limited
Tárgyszavak:Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
celiac disease
IgA nephropathy
tissue transglutaminase autoantibody
tissue transglutaminase-targeted IgA deposits
Megjelenés:Nutrients. - 13 : 5 (2021), p. 1-8. -
További szerzők:Korponay-Szabó Ilma (1959-) (gyermekgyógyász) Laurila, Kaija Huhtala, Heini Niemelä, Onni Mustonen, Jukka Mäkelä, Satu Kaukinen, Katri Lindfors, Katri
Pályázati támogatás:NKFIH 120392
Egyéb
Interreg Danube DTP571 CD SKILLS
Egyéb
GINOP-2.3.2-15-2016-00015
GINOP
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11.

001-es BibID:BIBFORM023716
Első szerző:Raivio, Tiina
Cím:Comparison of a novel whole blood transglutaminase-based ELISA with whole blood rapid antibody test and established conventional serological coeliac disease assays / Raivio T., Korponay-Szabó I. R., Paajanen T., Ashorn M., Iltanen S., Collin P., Laurila K., Nemes É., B. Kovács J., Carrard G., Saramaki M., Maki M., Kaukinen K.
Dátum:2008
Megjegyzések:Serum immunoglobulin A-class tissue transglutaminase (tTG-ab) and endomysial antibody (EMA) tests play a key role in the diagnostic evaluation of celiac disease. Recently, a novel whole blood rapid test based on self-tissue transglutaminase (tTG) was developed for celiac disease case finding. Based on the same principle, a whole blood self-tTG enzyme-linked immunosorbent assay (ELISA), especially applicable to large-scale screening of celiac disease, has been produced. We assessed the value of this new test in celiac disease antibody detection. PATIENTS AND METHODS: The new test uses endogenous tTG found in red blood cells of whole blood in IgA-class tTG-ab measurement by detecting tTG-tTG-ab complexes formed after hemolysis of the whole blood sample. Stored whole blood samples from 150 untreated celiac disease patients and 107 control individuals without celiac disease were evaluated, and the test results were compared with those of the whole blood rapid test, 2 conventional serum-based tTG-ab ELISA tests, and 2 EMA tests. RESULTS: A total of 15 whole blood samples were found to be clotted or dried after storage and were excluded from further evaluation. The whole blood ELISA test had a specificity (98%) comparable to that of the conventional serological tests, the sensitivity (91%) being slightly lower. The test was concordant with the whole blood rapid test in 92% of cases, with 2 serological ELISA tests in 91% and 94% of cases and with EMA tests in 94% and 93% of cases. CONCLUSIONS: Whole blood self-tTG-based testing is accurate in celiac antibody detection, also when an ELISA method is applied. The testing requires no serum separation or external tTG.
Tárgyszavak:Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
Megjelenés:Journal of Pediatric Gastroenterology and Nutrition. - 47 : 5 (2008), p. 562-567. -
További szerzők:Korponay-Szabó Ilma (1959-) (gyermekgyógyász) Paajanen, Tuula Ashorn, Merja Iltanen, Sari Collin, Pekka Laurila, Kaija Nemes Éva (1957-) (csecsemő- és gyermekgyógyász, gasztroenterológus) B. Kovács Judit Carrard, Géraldine Saramäki, Mika Mäki, Markku Kaukinen, Katri
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12.

001-es BibID:BIBFORM023665
Első szerző:Raivio, Tiina
Cím:Self transglutaminase-based rapid coeliac disease antibody detection by a lateral flow method / T. Raivio, K. Kaukinen, E. Nemes, K. Laurila, P. Collin, J. B. Kovács, M. Mäki, I. R. Korponay-Szabó
Dátum:2006
Megjegyzések:The conventional coeliac disease antibody tests require patient's sera, and are laborious and time-consuming. AIM: To evaluate a newly developed rapid whole blood test in coeliac disease antibody detection, and its suitability for office use. METHODS: Endogenous tissue transglutaminase found in red blood cells in a whole blood fingertip or venous sample is liberated upon haemolysis and complexes with tissue transglutaminase antibodies, if present. The complexes, captured by a lateral flow system, are visualized within 5 min. Stored samples from 121 untreated, 106 treated coeliac disease patients and 107 controls were evaluated and compared with serum endomysium and tissue transglutaminase antibody tests and histology; 150 patients were prospectively tested on site in the doctor's office. RESULTS: The rapid test showed sensitivity (96.7%) comparable with the serum endomysium and tissue transglutaminase antibody tests from stored samples; specificity was slightly lower (93.5%). When tested on site the results were concordant in 96.7% of cases compared with endomysium and tissue transglutaminase antibody results. The test recognized the disappearance of tissue transglutaminase antibodies on a gluten-free diet. CONCLUSIONS: The self tissue transglutaminase-based rapid test can be easily carried out from a fingertip blood sample on site in the physician's office for both coeliac disease case finding and dietary monitoring purposes.
Tárgyszavak:Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
Megjelenés:Alimentary Pharmacology & Therapeutics. - 24 : 1 (2006), p. 147-154. -
További szerzők:Kaukinen, Katri Nemes Éva (1957-) (csecsemő- és gyermekgyógyász, gasztroenterológus) Laurila, Kaija Collin, P. B. Kovács Judit Mäki, Markku Korponay-Szabó Ilma (1959-) (gyermekgyógyász)
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