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IL-10, IL-13, Eotaxin and IL-10/IL-6 ratio distinguish breast implant-associated anaplastic large-cell lymphoma from all types of benign late seromas
Breast implant-associated anaplastic large-cell lymphoma (BI-ALCL) is an uncommon peripheral T cell lymphoma usually presenting as a delayed peri-implant effusion. Chronic inflammation elicited by the implant has been implicated in its pathogenesis. Infection or implant rupture may also be responsib...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8053183/ https://www.ncbi.nlm.nih.gov/pubmed/33146828 http://dx.doi.org/10.1007/s00262-020-02778-3 |
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author | Di Napoli, Arianna Greco, Daniele Scafetta, Giorgia Ascenzi, Francesca Gulino, Alessandro Aurisicchio, Luigi Santanelli Di Pompeo, Fabio Bonifacino, Adriana Giarnieri, Enrico Morgan, John Mancini, Rita Kadin, Marshall E. |
author_facet | Di Napoli, Arianna Greco, Daniele Scafetta, Giorgia Ascenzi, Francesca Gulino, Alessandro Aurisicchio, Luigi Santanelli Di Pompeo, Fabio Bonifacino, Adriana Giarnieri, Enrico Morgan, John Mancini, Rita Kadin, Marshall E. |
author_sort | Di Napoli, Arianna |
collection | PubMed |
description | Breast implant-associated anaplastic large-cell lymphoma (BI-ALCL) is an uncommon peripheral T cell lymphoma usually presenting as a delayed peri-implant effusion. Chronic inflammation elicited by the implant has been implicated in its pathogenesis. Infection or implant rupture may also be responsible for late seromas. Cytomorphological examination coupled with CD30 immunostaining and eventual T-cell clonality assessment are essential for BI-ALCL diagnosis. However, some benign effusions may also contain an oligo/monoclonal expansion of CD30 + cells that can make the diagnosis challenging. Since cytokines are key mediators of inflammation, we applied a multiplexed immuno-based assay to BI-ALCL seromas and to different types of reactive seromas to look for a potential diagnostic BI-ALCL-associated cytokine profile. We found that BI-ALCL is characterized by a Th2-type cytokine milieu associated with significant high levels of IL-10, IL-13 and Eotaxin which discriminate BI-ALCL from all types of reactive seroma. Moreover, we found a cutoff of IL10/IL-6 ratio of 0.104 is associated with specificity of 100% and sensitivity of 83% in recognizing BI-ALCL effusions. This study identifies promising biomarkers for initial screening of late seromas that can facilitate early diagnosis of BI-ALCL. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00262-020-02778-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-8053183 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-80531832021-05-05 IL-10, IL-13, Eotaxin and IL-10/IL-6 ratio distinguish breast implant-associated anaplastic large-cell lymphoma from all types of benign late seromas Di Napoli, Arianna Greco, Daniele Scafetta, Giorgia Ascenzi, Francesca Gulino, Alessandro Aurisicchio, Luigi Santanelli Di Pompeo, Fabio Bonifacino, Adriana Giarnieri, Enrico Morgan, John Mancini, Rita Kadin, Marshall E. Cancer Immunol Immunother Original Article Breast implant-associated anaplastic large-cell lymphoma (BI-ALCL) is an uncommon peripheral T cell lymphoma usually presenting as a delayed peri-implant effusion. Chronic inflammation elicited by the implant has been implicated in its pathogenesis. Infection or implant rupture may also be responsible for late seromas. Cytomorphological examination coupled with CD30 immunostaining and eventual T-cell clonality assessment are essential for BI-ALCL diagnosis. However, some benign effusions may also contain an oligo/monoclonal expansion of CD30 + cells that can make the diagnosis challenging. Since cytokines are key mediators of inflammation, we applied a multiplexed immuno-based assay to BI-ALCL seromas and to different types of reactive seromas to look for a potential diagnostic BI-ALCL-associated cytokine profile. We found that BI-ALCL is characterized by a Th2-type cytokine milieu associated with significant high levels of IL-10, IL-13 and Eotaxin which discriminate BI-ALCL from all types of reactive seroma. Moreover, we found a cutoff of IL10/IL-6 ratio of 0.104 is associated with specificity of 100% and sensitivity of 83% in recognizing BI-ALCL effusions. This study identifies promising biomarkers for initial screening of late seromas that can facilitate early diagnosis of BI-ALCL. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00262-020-02778-3) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2020-11-04 2021 /pmc/articles/PMC8053183/ /pubmed/33146828 http://dx.doi.org/10.1007/s00262-020-02778-3 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 | Original Article Di Napoli, Arianna Greco, Daniele Scafetta, Giorgia Ascenzi, Francesca Gulino, Alessandro Aurisicchio, Luigi Santanelli Di Pompeo, Fabio Bonifacino, Adriana Giarnieri, Enrico Morgan, John Mancini, Rita Kadin, Marshall E. IL-10, IL-13, Eotaxin and IL-10/IL-6 ratio distinguish breast implant-associated anaplastic large-cell lymphoma from all types of benign late seromas |
title | IL-10, IL-13, Eotaxin and IL-10/IL-6 ratio distinguish breast implant-associated anaplastic large-cell lymphoma from all types of benign late seromas |
title_full | IL-10, IL-13, Eotaxin and IL-10/IL-6 ratio distinguish breast implant-associated anaplastic large-cell lymphoma from all types of benign late seromas |
title_fullStr | IL-10, IL-13, Eotaxin and IL-10/IL-6 ratio distinguish breast implant-associated anaplastic large-cell lymphoma from all types of benign late seromas |
title_full_unstemmed | IL-10, IL-13, Eotaxin and IL-10/IL-6 ratio distinguish breast implant-associated anaplastic large-cell lymphoma from all types of benign late seromas |
title_short | IL-10, IL-13, Eotaxin and IL-10/IL-6 ratio distinguish breast implant-associated anaplastic large-cell lymphoma from all types of benign late seromas |
title_sort | il-10, il-13, eotaxin and il-10/il-6 ratio distinguish breast implant-associated anaplastic large-cell lymphoma from all types of benign late seromas |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8053183/ https://www.ncbi.nlm.nih.gov/pubmed/33146828 http://dx.doi.org/10.1007/s00262-020-02778-3 |
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