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Corneal Langerhans cells in children with celiac disease
Celiac disease (CeD) is a common small bowel enteropathy characterized by an altered adaptive immune system and increased mucosal antigen presenting cells. This study aims to establish if quantification of corneal Langerhans cells (LCs) using corneal confocal microscopy (CCM) could act as a surrogat...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9622884/ https://www.ncbi.nlm.nih.gov/pubmed/36316419 http://dx.doi.org/10.1038/s41598-022-22376-w |
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author | Gad, Hoda Mohammed, Ibrahim Saraswathi, Saras Al-Jarrah, Bara Ferdousi, Maryam Petropoulos, Ioannis N. Ponirakis, Georgios Khan, Adnan Singh, Parul Al Khodor, Souhaila Elawad, Mamoun Almasri, Wesam Abdelrahman, Hatim Hussain, Khalid Hendaus, Mohamed A. Al-Mudahka, Fatma Abouhazima, Khaled Akobeng, Anthony K. Malik, Rayaz A. |
author_facet | Gad, Hoda Mohammed, Ibrahim Saraswathi, Saras Al-Jarrah, Bara Ferdousi, Maryam Petropoulos, Ioannis N. Ponirakis, Georgios Khan, Adnan Singh, Parul Al Khodor, Souhaila Elawad, Mamoun Almasri, Wesam Abdelrahman, Hatim Hussain, Khalid Hendaus, Mohamed A. Al-Mudahka, Fatma Abouhazima, Khaled Akobeng, Anthony K. Malik, Rayaz A. |
author_sort | Gad, Hoda |
collection | PubMed |
description | Celiac disease (CeD) is a common small bowel enteropathy characterized by an altered adaptive immune system and increased mucosal antigen presenting cells. This study aims to establish if quantification of corneal Langerhans cells (LCs) using corneal confocal microscopy (CCM) could act as a surrogate marker for antigen presenting cell status and hence disease activity in children with CeD. Twenty children with stable CeD and 20 age-matched controls underwent CCM and quantification of central corneal total, mature and immature LC density. There was no difference in age (11.78 ± 1.7 vs. 12.83 ± 1.91; P = 0.077) or height (1.38 ± 0.14 vs. 1.44 ± 0.13; P = 0.125). BMI (18.81 ± 3.90 vs. 22.26 ± 5.47; P = 0.031) and 25 OHD levels (43.50 ± 13.36 vs. 59.77 ± 22.45; P = 0.014) were significantly lower in children with CeD compared to controls. The total (33.33(16.67–59.37) vs. 51.56(30.21–85.42); P = 0.343), immature (33.33(16.67–52.08) vs. 44.79(29.17–82.29); P = 0.752) and mature (1.56(0–5) vs. 1.56(1.04–8.33); P = 0.752) LC density did not differ between the CeD and control groups. However, immature (r = 0.535, P = 0.015), mature (r = 0.464, P = 0.039), and total (r = 0.548, P = 0.012) LC density correlated with age. Immature (r = 0.602, P = 0.038) and total (r = 0.637, P = 0.026) LC density also correlated with tissue transglutaminase antibody (Anti-TtG) levels assessed in 12/20 subjects with CeD. There was no difference in corneal LC density between children with CeD and controls. However, the correlation between corneal LC density and anti-TtG levels suggests a relationship with disease activity in CeD and requires further study. |
format | Online Article Text |
id | pubmed-9622884 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96228842022-11-02 Corneal Langerhans cells in children with celiac disease Gad, Hoda Mohammed, Ibrahim Saraswathi, Saras Al-Jarrah, Bara Ferdousi, Maryam Petropoulos, Ioannis N. Ponirakis, Georgios Khan, Adnan Singh, Parul Al Khodor, Souhaila Elawad, Mamoun Almasri, Wesam Abdelrahman, Hatim Hussain, Khalid Hendaus, Mohamed A. Al-Mudahka, Fatma Abouhazima, Khaled Akobeng, Anthony K. Malik, Rayaz A. Sci Rep Article Celiac disease (CeD) is a common small bowel enteropathy characterized by an altered adaptive immune system and increased mucosal antigen presenting cells. This study aims to establish if quantification of corneal Langerhans cells (LCs) using corneal confocal microscopy (CCM) could act as a surrogate marker for antigen presenting cell status and hence disease activity in children with CeD. Twenty children with stable CeD and 20 age-matched controls underwent CCM and quantification of central corneal total, mature and immature LC density. There was no difference in age (11.78 ± 1.7 vs. 12.83 ± 1.91; P = 0.077) or height (1.38 ± 0.14 vs. 1.44 ± 0.13; P = 0.125). BMI (18.81 ± 3.90 vs. 22.26 ± 5.47; P = 0.031) and 25 OHD levels (43.50 ± 13.36 vs. 59.77 ± 22.45; P = 0.014) were significantly lower in children with CeD compared to controls. The total (33.33(16.67–59.37) vs. 51.56(30.21–85.42); P = 0.343), immature (33.33(16.67–52.08) vs. 44.79(29.17–82.29); P = 0.752) and mature (1.56(0–5) vs. 1.56(1.04–8.33); P = 0.752) LC density did not differ between the CeD and control groups. However, immature (r = 0.535, P = 0.015), mature (r = 0.464, P = 0.039), and total (r = 0.548, P = 0.012) LC density correlated with age. Immature (r = 0.602, P = 0.038) and total (r = 0.637, P = 0.026) LC density also correlated with tissue transglutaminase antibody (Anti-TtG) levels assessed in 12/20 subjects with CeD. There was no difference in corneal LC density between children with CeD and controls. However, the correlation between corneal LC density and anti-TtG levels suggests a relationship with disease activity in CeD and requires further study. Nature Publishing Group UK 2022-10-31 /pmc/articles/PMC9622884/ /pubmed/36316419 http://dx.doi.org/10.1038/s41598-022-22376-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Gad, Hoda Mohammed, Ibrahim Saraswathi, Saras Al-Jarrah, Bara Ferdousi, Maryam Petropoulos, Ioannis N. Ponirakis, Georgios Khan, Adnan Singh, Parul Al Khodor, Souhaila Elawad, Mamoun Almasri, Wesam Abdelrahman, Hatim Hussain, Khalid Hendaus, Mohamed A. Al-Mudahka, Fatma Abouhazima, Khaled Akobeng, Anthony K. Malik, Rayaz A. Corneal Langerhans cells in children with celiac disease |
title | Corneal Langerhans cells in children with celiac disease |
title_full | Corneal Langerhans cells in children with celiac disease |
title_fullStr | Corneal Langerhans cells in children with celiac disease |
title_full_unstemmed | Corneal Langerhans cells in children with celiac disease |
title_short | Corneal Langerhans cells in children with celiac disease |
title_sort | corneal langerhans cells in children with celiac disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9622884/ https://www.ncbi.nlm.nih.gov/pubmed/36316419 http://dx.doi.org/10.1038/s41598-022-22376-w |
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