Abstract
Mycosis fungoides (MF) is characterized by skin accumulation of CCR4+CCR7- effector memory T cells; however the mechanism for their recruitment is not clearly identified. Thymic Stromal Lymphopoietin (TSLP) is a keratinocyte-derived cytokine that triggers Th2 immunity and is associated with T cell recruitment to the skin in atopic dermatitis. Interleukin-16 (IL-16) is a chemoattractant and growth factor for CD4+ T cells. We hypothesized that TSLP and IL-16 could contribute to recruitment of malignant T cells in MF. We found elevated TSLP and IL-16 in very early stage patients' plasma and skin biopsies, prior to elevation in CCL22. Both TSLP and IL-16 induced migratory responses of CCR4+TSLPR+CD4+CCR7-CD31+ cells, characteristic of malignant T cells in the skin. Co-stimulation also resulted in significant proliferative responses. We conclude that TSLP and IL-16, expressed at early stages of disease, function to recruit malignant T cells to the skin and contribute to their enhanced proliferation.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 440-449 |
| Number of pages | 10 |
| Journal | Leukemia and Lymphoma |
| Volume | 56 |
| Issue number | 2 |
| DOIs | |
| State | Published - Feb 1 2015 |
Keywords
- Cutaneous T cell lymphoma (CTCL)
- Interleukin-16 (IL-16)
- Mycosis fungoides (MF)
- Thymic stromal lymphopoietin (TSLP)
ASJC Scopus subject areas
- Hematology
- Oncology
- Cancer Research
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