Plastic and Reconstructive Surgery, Global Open (Mar 2022)

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

  • 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

DOI
https://doi.org/10.1097/GOX.0000000000004148
Journal volume & issue
Vol. 10, no. 3
p. e4148

Abstract

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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.