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The association between eosinophils (CD16(+) eosinophils), basophils (CD203(+) basophils), and CD23 B lymphocytes in patients with atopic dermatitis on dupilumab therapy: pilot study
BACKGROUND: Eosinophils, basophils, and the molecule CD23 on B cells are involved in the pathophysiology of atopic dermatitis (AD). The molecule CD23 is involved in the regulation of IgE synthesis and is expressed by activated B cells. The molecule CD16 is used to assess the activation of eosinophil...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Healthcare
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10149537/ https://www.ncbi.nlm.nih.gov/pubmed/37071375 http://dx.doi.org/10.1007/s13555-023-00922-2 |
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author | Čelakovská, Jarmila Čermáková, Eva Boudková, Petra Andrýs, Ctirad Krejsek, Jan |
author_facet | Čelakovská, Jarmila Čermáková, Eva Boudková, Petra Andrýs, Ctirad Krejsek, Jan |
author_sort | Čelakovská, Jarmila |
collection | PubMed |
description | BACKGROUND: Eosinophils, basophils, and the molecule CD23 on B cells are involved in the pathophysiology of atopic dermatitis (AD). The molecule CD23 is involved in the regulation of IgE synthesis and is expressed by activated B cells. The molecule CD16 is used to assess the activation of eosinophils and CD203 of basophils. The association between the count of eosinophils, basophils, CD16(+) eosinophils, CD203(+) basophils and the expression of the activation marker CD23 on B cells in patients with AD (with and without dupilumab therapy) is not described. OBJECTIVE: The aim of this pilot study is to evaluate the association between the blood count of eosinophils, basophils, relative CD16(+) eosinophils, relative CD203(+) basophils, and the expression of molecule CD23 on B cells and on their subsets (total, memory, naive, switched, non-switched) in patients suffering from AD (with and without dupilumab therapy) and in control group. METHODS: A total of 45 patients suffering from AD were examined; 32 patients without dupilumab treatment (10 men, 22 women, average age 35 years), 13 patients with dupilumab treatment (7 men, 6 women, average age 43.4 years), and 30 subjects as a control group (10 men, 20 women, average age 44.7 years). Immunophenotype was examined by flow cytometry in which monoclonal antibodies with fluorescent molecules were used. For statistical analysis we used non-parametric Kruskal–Wallis one-factor analysis of variance with post hoc by Dunn’s test with Bonferroni modification and the Spearman’s rank correlation coefficient; for coefficients higher than 0.41, we report R(2) (percent of variation explained). RESULTS: The absolute count of eosinophils was significantly higher in patients with AD (with and without dupilumab) in comparison to healthy subjects. The difference in the relative count of CD16(+) eosinophils in patients with AD (with and without dupilumab therapy) compared with control is not statistically significant. In patients with dupilumab therapy the significantly lower count of relative CD203(+) basophils was confirmed compared with control. The higher association between the count of eosinophils (absolute and relative) and the expression of CD23 marker on B cells was confirmed in patients with dupilumab therapy; in contrast, this association was low in patients with AD without dupilumab therapy and in healthy subjects. CONCLUSION: The higher association between the count of eosinophils (absolute and relative) and the expression of CD23 marker on B cells was confirmed in patients with AD under dupilumab therapy. It suggests that IL-4 production by eosinophils may play a role in B lymphocyte activation. The significantly lower count of CD203(+) basophils has been demonstrated in patients with dupilumab therapy. This reduction of CD203(+) basophil count may contribute to the therapeutic effects of dupilumab by reducing the inflammatory response and allergic reactions in patients with AD. |
format | Online Article Text |
id | pubmed-10149537 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Healthcare |
record_format | MEDLINE/PubMed |
spelling | pubmed-101495372023-05-02 The association between eosinophils (CD16(+) eosinophils), basophils (CD203(+) basophils), and CD23 B lymphocytes in patients with atopic dermatitis on dupilumab therapy: pilot study Čelakovská, Jarmila Čermáková, Eva Boudková, Petra Andrýs, Ctirad Krejsek, Jan Dermatol Ther (Heidelb) Original Research BACKGROUND: Eosinophils, basophils, and the molecule CD23 on B cells are involved in the pathophysiology of atopic dermatitis (AD). The molecule CD23 is involved in the regulation of IgE synthesis and is expressed by activated B cells. The molecule CD16 is used to assess the activation of eosinophils and CD203 of basophils. The association between the count of eosinophils, basophils, CD16(+) eosinophils, CD203(+) basophils and the expression of the activation marker CD23 on B cells in patients with AD (with and without dupilumab therapy) is not described. OBJECTIVE: The aim of this pilot study is to evaluate the association between the blood count of eosinophils, basophils, relative CD16(+) eosinophils, relative CD203(+) basophils, and the expression of molecule CD23 on B cells and on their subsets (total, memory, naive, switched, non-switched) in patients suffering from AD (with and without dupilumab therapy) and in control group. METHODS: A total of 45 patients suffering from AD were examined; 32 patients without dupilumab treatment (10 men, 22 women, average age 35 years), 13 patients with dupilumab treatment (7 men, 6 women, average age 43.4 years), and 30 subjects as a control group (10 men, 20 women, average age 44.7 years). Immunophenotype was examined by flow cytometry in which monoclonal antibodies with fluorescent molecules were used. For statistical analysis we used non-parametric Kruskal–Wallis one-factor analysis of variance with post hoc by Dunn’s test with Bonferroni modification and the Spearman’s rank correlation coefficient; for coefficients higher than 0.41, we report R(2) (percent of variation explained). RESULTS: The absolute count of eosinophils was significantly higher in patients with AD (with and without dupilumab) in comparison to healthy subjects. The difference in the relative count of CD16(+) eosinophils in patients with AD (with and without dupilumab therapy) compared with control is not statistically significant. In patients with dupilumab therapy the significantly lower count of relative CD203(+) basophils was confirmed compared with control. The higher association between the count of eosinophils (absolute and relative) and the expression of CD23 marker on B cells was confirmed in patients with dupilumab therapy; in contrast, this association was low in patients with AD without dupilumab therapy and in healthy subjects. CONCLUSION: The higher association between the count of eosinophils (absolute and relative) and the expression of CD23 marker on B cells was confirmed in patients with AD under dupilumab therapy. It suggests that IL-4 production by eosinophils may play a role in B lymphocyte activation. The significantly lower count of CD203(+) basophils has been demonstrated in patients with dupilumab therapy. This reduction of CD203(+) basophil count may contribute to the therapeutic effects of dupilumab by reducing the inflammatory response and allergic reactions in patients with AD. Springer Healthcare 2023-04-18 /pmc/articles/PMC10149537/ /pubmed/37071375 http://dx.doi.org/10.1007/s13555-023-00922-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc/4.0/Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial 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-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Original Research Čelakovská, Jarmila Čermáková, Eva Boudková, Petra Andrýs, Ctirad Krejsek, Jan The association between eosinophils (CD16(+) eosinophils), basophils (CD203(+) basophils), and CD23 B lymphocytes in patients with atopic dermatitis on dupilumab therapy: pilot study |
title | The association between eosinophils (CD16(+) eosinophils), basophils (CD203(+) basophils), and CD23 B lymphocytes in patients with atopic dermatitis on dupilumab therapy: pilot study |
title_full | The association between eosinophils (CD16(+) eosinophils), basophils (CD203(+) basophils), and CD23 B lymphocytes in patients with atopic dermatitis on dupilumab therapy: pilot study |
title_fullStr | The association between eosinophils (CD16(+) eosinophils), basophils (CD203(+) basophils), and CD23 B lymphocytes in patients with atopic dermatitis on dupilumab therapy: pilot study |
title_full_unstemmed | The association between eosinophils (CD16(+) eosinophils), basophils (CD203(+) basophils), and CD23 B lymphocytes in patients with atopic dermatitis on dupilumab therapy: pilot study |
title_short | The association between eosinophils (CD16(+) eosinophils), basophils (CD203(+) basophils), and CD23 B lymphocytes in patients with atopic dermatitis on dupilumab therapy: pilot study |
title_sort | association between eosinophils (cd16(+) eosinophils), basophils (cd203(+) basophils), and cd23 b lymphocytes in patients with atopic dermatitis on dupilumab therapy: pilot study |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10149537/ https://www.ncbi.nlm.nih.gov/pubmed/37071375 http://dx.doi.org/10.1007/s13555-023-00922-2 |
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