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Serum carbonic anhydrase I and II autoantibodies in patients with chronic lymphocytic leukaemia

Cancer is the second most important cause of mortality, and millions of people either have or have had the disease. Leukaemia is one of the most common forms of cancer. Autoantibodies that have developed against the organism’s self-antigens are detected in the sera of subjects with cancer. In recent...

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Autores principales: Mentese, Ahmet, Erkut, Nergiz, Demir, Selim, Yaman, Serap Ozer, Sumer, Aysegul, Erdem, Mehmet, Alver, Ahmet, Sonmez, Mehmet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Polish Society of Experimental and Clinical Immunology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305617/
https://www.ncbi.nlm.nih.gov/pubmed/30588172
http://dx.doi.org/10.5114/ceji.2018.80046
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author Mentese, Ahmet
Erkut, Nergiz
Demir, Selim
Yaman, Serap Ozer
Sumer, Aysegul
Erdem, Mehmet
Alver, Ahmet
Sonmez, Mehmet
author_facet Mentese, Ahmet
Erkut, Nergiz
Demir, Selim
Yaman, Serap Ozer
Sumer, Aysegul
Erdem, Mehmet
Alver, Ahmet
Sonmez, Mehmet
author_sort Mentese, Ahmet
collection PubMed
description Cancer is the second most important cause of mortality, and millions of people either have or have had the disease. Leukaemia is one of the most common forms of cancer. Autoantibodies that have developed against the organism’s self-antigens are detected in the sera of subjects with cancer. In recent years carbonic anhydrase (CA) autoantibodies have been determined in some autoimmune diseases and carcinomas, but the mechanisms underlying this immune response have not yet been fully explained. The purpose of this study was to determine CA I and II autoantibodies in subjects with chronic lymphocytic leukaemia (CLL) and to provide a novel perspective regarding the autoimmune basis of the disease. Autoantibody levels were investigated using enzyme-linked immunosorbent assay (ELISA) in serum samples from 37 patients with CLL and 37 healthy peers. Anti-CA I titres in the CLL group were significantly higher compared with the control group (p = 0.0001). However, there was no significant difference between CLL and control groups in terms of anti-CA II titres (p = 0.278). The prevalences of CA I and II autoantibodies in patients with CLL in this study were 27% and 24.3%, respectively. Our results suggest that these autoantibodies may be involved in the pathogenesis of CLL. More extensive studies are now needed to reveal the entire mechanism.
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spelling pubmed-63056172018-12-26 Serum carbonic anhydrase I and II autoantibodies in patients with chronic lymphocytic leukaemia Mentese, Ahmet Erkut, Nergiz Demir, Selim Yaman, Serap Ozer Sumer, Aysegul Erdem, Mehmet Alver, Ahmet Sonmez, Mehmet Cent Eur J Immunol Clinical Immunology Cancer is the second most important cause of mortality, and millions of people either have or have had the disease. Leukaemia is one of the most common forms of cancer. Autoantibodies that have developed against the organism’s self-antigens are detected in the sera of subjects with cancer. In recent years carbonic anhydrase (CA) autoantibodies have been determined in some autoimmune diseases and carcinomas, but the mechanisms underlying this immune response have not yet been fully explained. The purpose of this study was to determine CA I and II autoantibodies in subjects with chronic lymphocytic leukaemia (CLL) and to provide a novel perspective regarding the autoimmune basis of the disease. Autoantibody levels were investigated using enzyme-linked immunosorbent assay (ELISA) in serum samples from 37 patients with CLL and 37 healthy peers. Anti-CA I titres in the CLL group were significantly higher compared with the control group (p = 0.0001). However, there was no significant difference between CLL and control groups in terms of anti-CA II titres (p = 0.278). The prevalences of CA I and II autoantibodies in patients with CLL in this study were 27% and 24.3%, respectively. Our results suggest that these autoantibodies may be involved in the pathogenesis of CLL. More extensive studies are now needed to reveal the entire mechanism. Polish Society of Experimental and Clinical Immunology 2018-10-30 2018 /pmc/articles/PMC6305617/ /pubmed/30588172 http://dx.doi.org/10.5114/ceji.2018.80046 Text en Copyright: © 2018 Polish Society of Experimental and Clinical Immunology http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Clinical Immunology
Mentese, Ahmet
Erkut, Nergiz
Demir, Selim
Yaman, Serap Ozer
Sumer, Aysegul
Erdem, Mehmet
Alver, Ahmet
Sonmez, Mehmet
Serum carbonic anhydrase I and II autoantibodies in patients with chronic lymphocytic leukaemia
title Serum carbonic anhydrase I and II autoantibodies in patients with chronic lymphocytic leukaemia
title_full Serum carbonic anhydrase I and II autoantibodies in patients with chronic lymphocytic leukaemia
title_fullStr Serum carbonic anhydrase I and II autoantibodies in patients with chronic lymphocytic leukaemia
title_full_unstemmed Serum carbonic anhydrase I and II autoantibodies in patients with chronic lymphocytic leukaemia
title_short Serum carbonic anhydrase I and II autoantibodies in patients with chronic lymphocytic leukaemia
title_sort serum carbonic anhydrase i and ii autoantibodies in patients with chronic lymphocytic leukaemia
topic Clinical Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305617/
https://www.ncbi.nlm.nih.gov/pubmed/30588172
http://dx.doi.org/10.5114/ceji.2018.80046
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