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Low prevalence of liver-kidney microsomal autoantibodies of type 1 (LKM(1)) in hepatitis C seropositive subjects on Crete, Greece

BACKGROUND: Hepatitis C is a serious problem on the Greek island of Crete, where a high prevalence of antibodies against hepatitis C (anti-HCV) has recently been reported. This article reports the findings of a study carried out in Crete, which investigated the prevalence of serum autoantibodies in...

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Autores principales: Drygiannakis, Dimitrios, Lionis, Christos, Drygiannakis, Ioannis, Pappas, Georgios, Kouroumalis, Elias
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2001
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC33343/
https://www.ncbi.nlm.nih.gov/pubmed/11418082
http://dx.doi.org/10.1186/1471-230X-1-4
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author Drygiannakis, Dimitrios
Lionis, Christos
Drygiannakis, Ioannis
Pappas, Georgios
Kouroumalis, Elias
author_facet Drygiannakis, Dimitrios
Lionis, Christos
Drygiannakis, Ioannis
Pappas, Georgios
Kouroumalis, Elias
author_sort Drygiannakis, Dimitrios
collection PubMed
description BACKGROUND: Hepatitis C is a serious problem on the Greek island of Crete, where a high prevalence of antibodies against hepatitis C (anti-HCV) has recently been reported. This article reports the findings of a study carried out in Crete, which investigated the prevalence of serum autoantibodies in patients with chronic hepatitis C. PATIENTS AND METHODS: One hundred and forty two patients (59 men and 83 women), who were found anti-HCV seropositive in two hospitals and two Primary Health Care Centres in Crete, were eligible. Sixty healthy blood donors (46 men, 14 women), which were negative to anti-HCV, were used as the control group. They were randomly selected from those attending Rethymnon Hospital. Autoantibodies were identified using the indirect immunofluorescence (IFL) technique on human epithelial cells from larynx cancer (HEp-2 cells), rat liver-kidney-stomach substrate (CT3) and Chrithidia Luciliae (CL). RESULTS: Serum autoantibodies were detected in 104 HCV patients, yielding an overall prevalence of 73.2%. The most frequent autoantibodies were antinuclear antibodies (ANA), positive in 72 patients (50.7%). Anti-smooth muscle antibodies (ASMA) were detected in 33 patients (23.2%). Only one patient was positive for LKM(1) autoantibodies. No autoantibodies were found in 38 patients (26.7%). Autoantibodies were also found in 5 out of the 60 examined healthy blood donors (8.3%). CONCLUSIONS: Autoantibodies, mainly ANA and ASMA are very common in HCV seropositive patients from Crete. By contrast LKM(1) autoantibodies are exceptionally rare in these patients.
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spelling pubmed-333432001-06-21 Low prevalence of liver-kidney microsomal autoantibodies of type 1 (LKM(1)) in hepatitis C seropositive subjects on Crete, Greece Drygiannakis, Dimitrios Lionis, Christos Drygiannakis, Ioannis Pappas, Georgios Kouroumalis, Elias BMC Gastroenterol Research Article BACKGROUND: Hepatitis C is a serious problem on the Greek island of Crete, where a high prevalence of antibodies against hepatitis C (anti-HCV) has recently been reported. This article reports the findings of a study carried out in Crete, which investigated the prevalence of serum autoantibodies in patients with chronic hepatitis C. PATIENTS AND METHODS: One hundred and forty two patients (59 men and 83 women), who were found anti-HCV seropositive in two hospitals and two Primary Health Care Centres in Crete, were eligible. Sixty healthy blood donors (46 men, 14 women), which were negative to anti-HCV, were used as the control group. They were randomly selected from those attending Rethymnon Hospital. Autoantibodies were identified using the indirect immunofluorescence (IFL) technique on human epithelial cells from larynx cancer (HEp-2 cells), rat liver-kidney-stomach substrate (CT3) and Chrithidia Luciliae (CL). RESULTS: Serum autoantibodies were detected in 104 HCV patients, yielding an overall prevalence of 73.2%. The most frequent autoantibodies were antinuclear antibodies (ANA), positive in 72 patients (50.7%). Anti-smooth muscle antibodies (ASMA) were detected in 33 patients (23.2%). Only one patient was positive for LKM(1) autoantibodies. No autoantibodies were found in 38 patients (26.7%). Autoantibodies were also found in 5 out of the 60 examined healthy blood donors (8.3%). CONCLUSIONS: Autoantibodies, mainly ANA and ASMA are very common in HCV seropositive patients from Crete. By contrast LKM(1) autoantibodies are exceptionally rare in these patients. BioMed Central 2001-06-11 /pmc/articles/PMC33343/ /pubmed/11418082 http://dx.doi.org/10.1186/1471-230X-1-4 Text en Copyright © 2001 Drygiannakis et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Research Article
Drygiannakis, Dimitrios
Lionis, Christos
Drygiannakis, Ioannis
Pappas, Georgios
Kouroumalis, Elias
Low prevalence of liver-kidney microsomal autoantibodies of type 1 (LKM(1)) in hepatitis C seropositive subjects on Crete, Greece
title Low prevalence of liver-kidney microsomal autoantibodies of type 1 (LKM(1)) in hepatitis C seropositive subjects on Crete, Greece
title_full Low prevalence of liver-kidney microsomal autoantibodies of type 1 (LKM(1)) in hepatitis C seropositive subjects on Crete, Greece
title_fullStr Low prevalence of liver-kidney microsomal autoantibodies of type 1 (LKM(1)) in hepatitis C seropositive subjects on Crete, Greece
title_full_unstemmed Low prevalence of liver-kidney microsomal autoantibodies of type 1 (LKM(1)) in hepatitis C seropositive subjects on Crete, Greece
title_short Low prevalence of liver-kidney microsomal autoantibodies of type 1 (LKM(1)) in hepatitis C seropositive subjects on Crete, Greece
title_sort low prevalence of liver-kidney microsomal autoantibodies of type 1 (lkm(1)) in hepatitis c seropositive subjects on crete, greece
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC33343/
https://www.ncbi.nlm.nih.gov/pubmed/11418082
http://dx.doi.org/10.1186/1471-230X-1-4
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