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Tissue Expander–associated T Cells: Relevance to Breast Implant–associated Anaplastic Large-cell Lymphoma
The generation of breast implant–associated anaplastic large-cell lymphoma (BIA-ALCL) is closely associated with textured implants. The phenotype of BIA-ALCL cells is well examined, but its cell of origin remains unknown. Here we investigate what types of T cells are recruited and differentiated in...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8942776/ https://www.ncbi.nlm.nih.gov/pubmed/35356046 http://dx.doi.org/10.1097/GOX.0000000000004148 |
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author | Shiokawa, Ichiro Sato, Takuya Ogawa, Youichi Nagasaka, Yuka Ishikawa, Aoha Shimada, Shinji Kawamura, Tatsuyoshi Momosawa, Akira |
author_facet | Shiokawa, Ichiro Sato, Takuya Ogawa, Youichi Nagasaka, Yuka Ishikawa, Aoha Shimada, Shinji Kawamura, Tatsuyoshi Momosawa, Akira |
author_sort | Shiokawa, Ichiro |
collection | PubMed |
description | The generation of breast implant–associated anaplastic large-cell lymphoma (BIA-ALCL) is closely associated with textured implants. The phenotype of BIA-ALCL cells is well examined, but its cell of origin remains unknown. Here we investigate what types of T cells are recruited and differentiated in the surrounding capsules and tissues as a consequence of continuous contact with a textured surface. METHODS: Capsule and pericapsule tissues were recovered from patients who had textured or smooth tissue expanders (TEs). These samples were enzymatically digested, and T cells in the samples were analyzed using flow cytometry. Peripheral blood mononuclear cells from the same donors were utilized as a control. RESULTS: Effector memory CD4(+) T cells predominantly infiltrated capsules and tissues without apparent differences between textured and smooth TEs. In these effector memory CD4(+) T cells, CD4(+) resident memory T cells were generated by smooth TEs but not by textured TEs. However, TNFRSF8/CD30 mRNA expression is higher in the CD69(−) effector memory CD4(+) T cells than in the CD69(+) ones. CONCLUSION: Textured and smooth TEs differentially recruit and/or differentiate T cells in situ. |
format | Online Article Text |
id | pubmed-8942776 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-89427762022-03-29 Tissue Expander–associated T Cells: Relevance to Breast Implant–associated Anaplastic Large-cell Lymphoma Shiokawa, Ichiro Sato, Takuya Ogawa, Youichi Nagasaka, Yuka Ishikawa, Aoha Shimada, Shinji Kawamura, Tatsuyoshi Momosawa, Akira Plast Reconstr Surg Glob Open Research The generation of breast implant–associated anaplastic large-cell lymphoma (BIA-ALCL) is closely associated with textured implants. The phenotype of BIA-ALCL cells is well examined, but its cell of origin remains unknown. Here we investigate what types of T cells are recruited and differentiated in the surrounding capsules and tissues as a consequence of continuous contact with a textured surface. METHODS: Capsule and pericapsule tissues were recovered from patients who had textured or smooth tissue expanders (TEs). These samples were enzymatically digested, and T cells in the samples were analyzed using flow cytometry. Peripheral blood mononuclear cells from the same donors were utilized as a control. RESULTS: Effector memory CD4(+) T cells predominantly infiltrated capsules and tissues without apparent differences between textured and smooth TEs. In these effector memory CD4(+) T cells, CD4(+) resident memory T cells were generated by smooth TEs but not by textured TEs. However, TNFRSF8/CD30 mRNA expression is higher in the CD69(−) effector memory CD4(+) T cells than in the CD69(+) ones. CONCLUSION: Textured and smooth TEs differentially recruit and/or differentiate T cells in situ. Lippincott Williams & Wilkins 2022-03-23 /pmc/articles/PMC8942776/ /pubmed/35356046 http://dx.doi.org/10.1097/GOX.0000000000004148 Text en Copyright © 2022 The Authors. Published by Wolters Kluwer Health, Inc. on behalf of The American Society of Plastic Surgeons. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Research Shiokawa, Ichiro Sato, Takuya Ogawa, Youichi Nagasaka, Yuka Ishikawa, Aoha Shimada, Shinji Kawamura, Tatsuyoshi Momosawa, Akira Tissue Expander–associated T Cells: Relevance to Breast Implant–associated Anaplastic Large-cell Lymphoma |
title | Tissue Expander–associated T Cells: Relevance to Breast Implant–associated Anaplastic Large-cell Lymphoma |
title_full | Tissue Expander–associated T Cells: Relevance to Breast Implant–associated Anaplastic Large-cell Lymphoma |
title_fullStr | Tissue Expander–associated T Cells: Relevance to Breast Implant–associated Anaplastic Large-cell Lymphoma |
title_full_unstemmed | Tissue Expander–associated T Cells: Relevance to Breast Implant–associated Anaplastic Large-cell Lymphoma |
title_short | Tissue Expander–associated T Cells: Relevance to Breast Implant–associated Anaplastic Large-cell Lymphoma |
title_sort | tissue expander–associated t cells: relevance to breast implant–associated anaplastic large-cell lymphoma |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8942776/ https://www.ncbi.nlm.nih.gov/pubmed/35356046 http://dx.doi.org/10.1097/GOX.0000000000004148 |
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