Tissue Expander–associated T Cells: Relevance to Breast Implant–associated Anaplastic Large-cell Lymphoma

Background:. 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 diffe...

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Bibliographic Details
Main Authors: Ichiro Shiokawa, MD, Takuya Sato, MS, Youichi Ogawa, MD, PhD, Yuka Nagasaka, MD, Aoha Ishikawa, MD, Shinji Shimada, MD, PhD, Tatsuyoshi Kawamura, MD, PhD, Akira Momosawa, MD, PhD
Format: Article
Language:English
Published: Wolters Kluwer 2022-03-01
Series:Plastic and Reconstructive Surgery, Global Open
Online Access:http://journals.lww.com/prsgo/fulltext/10.1097/GOX.0000000000004148
Description
Summary:Background:. 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.
ISSN:2169-7574