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Published on: December 6, 2014
Phenotype of lymphocytes associated with the inflammatory reaction to silicone gel breast implants
W E Katzin1, L J Feng, M Abbuhl
1Department of Pathology, Mt. Sinai Medical Center, Cleveland, OH 44106, USA.
Insights
Silicone gel breast implants trigger an immune response, activating T cells (a type of lymphocyte) within the fibrous capsule. This immune activation suggests a potential for antibody production, warranting further study.
Area of Science:
- Immunology
- Biomaterials Science
- Pathology
Background:
- Silicone gel breast implants elicit a tissue response involving inflammatory cells.
- Lymphocytes are a key component of this inflammatory infiltrate.
- Understanding lymphocyte phenotype is crucial for assessing implant-associated immune responses.
Purpose of the Study:
- To investigate the phenotype of lymphocytes associated with silicone gel breast implants.
- To determine the activation status of these lymphocytes.
- To explore the potential clinical significance of the observed immune activation.
Main Methods:
- Collection of fluid and cells from the implant-capsule interface and fibrous capsule.
- Utilizing three-color flow cytometry to analyze lymphocyte populations.
- Characterization of T cell subsets (CD3+, CD4+, CD29+, CD45RO+) and HLA-DR expression.
Main Results:
- Implant-associated lymphocytes were predominantly T cells (89%).
- A significantly higher proportion of T cells expressed HLA-DR (25%) compared to peripheral blood (7.9%).
- A majority of T cells coexpressed CD4 and CD29 (68%), indicating an activated phenotype.
Conclusions:
- Silicone gel breast implants induce immune activation, characterized by specific T cell phenotypes.
- The presence of activated T cells suggests a potential for stimulating antigen-specific antibody production.
- Further research is needed to elucidate the clinical implications of this immune activation.
Abstract:
The tissue response to silicone gel breast implants typically includes an inflammatory infiltrate that consists of macrophages, foreign body-type giant cells, and a variable number of lymphocytes and plasma cells. The phenotype of the lymphocytic component was investigated with three-color flow cytometry. Lymphocytes were obtained by collecting fluid from the space between the implant and the fibrous capsule or by washing cells from the fibrous capsule at the time of implant removal with total capsulectomy. Eighty-nine percent of the implant-associated lymphocytes were T cells. Twenty-five percent of the CD3+ T cells coexpressed HLA-DR compared with only 7.9% of matched peripheral blood lymphocytes. Sixty-eight percent of the implant-associated T cells coexpressed CD4 and CD29, while only 3% of the T cells coexpressed CD4 and CD45RO. The expression of HLA-DR and the predominance of CD29+ CD4+ T cells indicate that there is immune activation with the potential for stimulating antigen-specific antibody production. The role of silicone gel breast implants in immune activation and its clinical significance require further investigation.
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