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Small-intestinal TG2-specific plasma cells at different stages of coeliac disease

BACKGROUND: In coeliac disease, ingestion of gluten induces the production of transglutaminase 2 (TG2)-targeted autoantibodies by TG2-specific plasma cells present at high frequency in the small intestinal mucosa in untreated disease. During treatment with a gluten-free diet (GFD), the number of the...

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Autores principales: Hietikko, Minna, Koskinen, Outi, Kurppa, Kalle, Laurila, Kaija, Saavalainen, Päivi, Salmi, Teea, Ilus, Tuire, Huhtala, Heini, Kaukinen, Katri, Lindfors, Katri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6282384/
https://www.ncbi.nlm.nih.gov/pubmed/30522434
http://dx.doi.org/10.1186/s12865-018-0275-7
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author Hietikko, Minna
Koskinen, Outi
Kurppa, Kalle
Laurila, Kaija
Saavalainen, Päivi
Salmi, Teea
Ilus, Tuire
Huhtala, Heini
Kaukinen, Katri
Lindfors, Katri
author_facet Hietikko, Minna
Koskinen, Outi
Kurppa, Kalle
Laurila, Kaija
Saavalainen, Päivi
Salmi, Teea
Ilus, Tuire
Huhtala, Heini
Kaukinen, Katri
Lindfors, Katri
author_sort Hietikko, Minna
collection PubMed
description BACKGROUND: In coeliac disease, ingestion of gluten induces the production of transglutaminase 2 (TG2)-targeted autoantibodies by TG2-specific plasma cells present at high frequency in the small intestinal mucosa in untreated disease. During treatment with a gluten-free diet (GFD), the number of these cells decreases considerably. It has not been previously investigated whether the cells are also present prior to development of villous atrophy, or in non-responsive patients and those with dietary lapses. We aimed to define the frequency of small bowel mucosal TG2-specific plasma cells in coeliac disease patients with varying disease activity, and to investigate whether the frequency correlates with serum and small intestinal TG2-targeting antibodies as well as mucosal morphology and the number of intraepithelial lymphocytes. RESULTS: Mucosal TG2-specific plasma cells were found in 79% of patients prior to development of mucosal damage, in all patients with villous atrophy, and in 63% of the patients after 1 year on GFD. In these disease stages, TG2-specific plasma cells accounted for median of 2.3, 4.3, and 0.7% of all mucosal plasma cells, respectively. After long-term treatment, the cells were present in 20% of the patients in clinical remission (median 0%) and in 60% of the patients with poor dietary adherence (median 5.8%). In patients with non-responsive coeliac disease despite strict GFD, the cells were found in only one (9%) subject; the cells accounted for 2.4% of all plasma cells. A positive correlation between the percentage of TG2-specific plasma cells and serum TG2 antibody levels (r(S) = 0.69, P < 0.001) and the intensity of mucosal TG2-targeting IgA deposits (r(S) = 0.43, P < 0.001) was observed. CONCLUSIONS: Our results show that TG2-specific plasma cells are already detectable prior to villous atrophy, and that generally their frequency increases during overt disease. By contrast, on GFD, the percentage of these cells decreases. Overall, the presence of TG2-specific plasma cells in the small bowel mucosa mirrors the presence of gluten in the diet, but the frequency is not always parallel to the level of serum or intestinal TG2 antibodies. These findings increase the knowledge about the development of the TG2 plasma cell responses especially in the early phases of coeliac disease. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12865-018-0275-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-62823842018-12-14 Small-intestinal TG2-specific plasma cells at different stages of coeliac disease Hietikko, Minna Koskinen, Outi Kurppa, Kalle Laurila, Kaija Saavalainen, Päivi Salmi, Teea Ilus, Tuire Huhtala, Heini Kaukinen, Katri Lindfors, Katri BMC Immunol Research Article BACKGROUND: In coeliac disease, ingestion of gluten induces the production of transglutaminase 2 (TG2)-targeted autoantibodies by TG2-specific plasma cells present at high frequency in the small intestinal mucosa in untreated disease. During treatment with a gluten-free diet (GFD), the number of these cells decreases considerably. It has not been previously investigated whether the cells are also present prior to development of villous atrophy, or in non-responsive patients and those with dietary lapses. We aimed to define the frequency of small bowel mucosal TG2-specific plasma cells in coeliac disease patients with varying disease activity, and to investigate whether the frequency correlates with serum and small intestinal TG2-targeting antibodies as well as mucosal morphology and the number of intraepithelial lymphocytes. RESULTS: Mucosal TG2-specific plasma cells were found in 79% of patients prior to development of mucosal damage, in all patients with villous atrophy, and in 63% of the patients after 1 year on GFD. In these disease stages, TG2-specific plasma cells accounted for median of 2.3, 4.3, and 0.7% of all mucosal plasma cells, respectively. After long-term treatment, the cells were present in 20% of the patients in clinical remission (median 0%) and in 60% of the patients with poor dietary adherence (median 5.8%). In patients with non-responsive coeliac disease despite strict GFD, the cells were found in only one (9%) subject; the cells accounted for 2.4% of all plasma cells. A positive correlation between the percentage of TG2-specific plasma cells and serum TG2 antibody levels (r(S) = 0.69, P < 0.001) and the intensity of mucosal TG2-targeting IgA deposits (r(S) = 0.43, P < 0.001) was observed. CONCLUSIONS: Our results show that TG2-specific plasma cells are already detectable prior to villous atrophy, and that generally their frequency increases during overt disease. By contrast, on GFD, the percentage of these cells decreases. Overall, the presence of TG2-specific plasma cells in the small bowel mucosa mirrors the presence of gluten in the diet, but the frequency is not always parallel to the level of serum or intestinal TG2 antibodies. These findings increase the knowledge about the development of the TG2 plasma cell responses especially in the early phases of coeliac disease. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12865-018-0275-7) contains supplementary material, which is available to authorized users. BioMed Central 2018-12-06 /pmc/articles/PMC6282384/ /pubmed/30522434 http://dx.doi.org/10.1186/s12865-018-0275-7 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Hietikko, Minna
Koskinen, Outi
Kurppa, Kalle
Laurila, Kaija
Saavalainen, Päivi
Salmi, Teea
Ilus, Tuire
Huhtala, Heini
Kaukinen, Katri
Lindfors, Katri
Small-intestinal TG2-specific plasma cells at different stages of coeliac disease
title Small-intestinal TG2-specific plasma cells at different stages of coeliac disease
title_full Small-intestinal TG2-specific plasma cells at different stages of coeliac disease
title_fullStr Small-intestinal TG2-specific plasma cells at different stages of coeliac disease
title_full_unstemmed Small-intestinal TG2-specific plasma cells at different stages of coeliac disease
title_short Small-intestinal TG2-specific plasma cells at different stages of coeliac disease
title_sort small-intestinal tg2-specific plasma cells at different stages of coeliac disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6282384/
https://www.ncbi.nlm.nih.gov/pubmed/30522434
http://dx.doi.org/10.1186/s12865-018-0275-7
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