Decreased IL-10-producing regulatory B cells in patients with advanced mycosis fungoides

Eur J Dermatol. 2018 Jun 1;28(3):314-319. doi: 10.1684/ejd.2018.3319.

Abstract

Background: Historically, B cells have been considered as positive regulators of humoral immune responses. Specific B-cell subsets, however, negatively regulate immune responses and are termed "regulatory B cells" (Bregs). Recently, Bregs have been linked to not only inflammatory and autoimmune diseases, but also malignancies via suppressing anti-tumour immunity.

Objectives: To investigate the involvement of Bregs in advanced mycosis fungoides (MF).

Materials & methods: The frequency of CD19+CD24hiCD27+ memory B cells and CD19+CD24hiCD38hi transitional B cells (which enrich IL-10-producing Bregs) was examined in peripheral blood from patients with advanced MF (n = 11) and healthy controls (n = 9) by flow cytometry. The frequency of IL-10-producing Bregs was also measured by flow cytometry. The correlation between frequency or number of B-cell subsets and disease severity markers was also analysed.

Results: The frequency of CD19+CD24hiCD27+ B cells, CD19+CD24hiCD38hi B cells, and IL-10-producing B cells was decreased in peripheral blood of advanced MF patients. The frequency and number of these B-cell subsets inversely correlated with serum soluble IL-2 receptor and serum lactate dehydrogenase levels.

Conclusions: The development of IL-10-producing Bregs is impaired in patients with advanced MF and a decrease in IL-10-producing Bregs may play an important role in the progression of advanced MF.

Keywords: B cells; IL-10; mycosis fungoides; regulatory B cells (Bregs).

MeSH terms

  • Adult
  • Aged
  • Antigens, CD / blood
  • B-Lymphocytes, Regulatory / immunology*
  • Disease Progression
  • Female
  • Humans
  • Interleukin-10 / blood*
  • L-Lactate Dehydrogenase / blood
  • Lymphocyte Count
  • Male
  • Middle Aged
  • Mycosis Fungoides / immunology*
  • Receptors, Interleukin-2 / blood
  • Skin / immunology
  • Skin Neoplasms / immunology*

Substances

  • Antigens, CD
  • Receptors, Interleukin-2
  • Interleukin-10
  • L-Lactate Dehydrogenase