Variable levels of apoptotic signal-associated cytokines in the disease course of patients with Stevens-Johnson syndrome and toxic epidermal necrolysis

Australas J Dermatol. 2017 Aug;58(3):e61-e67. doi: 10.1111/ajd.12462. Epub 2016 Apr 3.

Abstract

Background/objectives: Keratinocyte death is a hallmark of Stevens-Johnson syndrome and toxic epidermal necrolysis (SJS/TEN). Apoptotic signal-associated cytokines, such as TNF-α, sFasL, granulysin, sTRAIL and IFN-γ have been reported to participate in keratinocyte apoptosis. However, their levels are variable, which hampers the elucidation of the role of these cytokines. We sought to determine whether cytokine levels vary with disease course.

Methods: The serum cytokine levels of 24 patients and blister fluid of 10 were analysed by enzyme-linked immunosorbent assay on the first day of their admission to hospital and were evaluated at different time points in the disease course. Meanwhile, surface markers (CD3, CD4, CD8, CD1a, CD14, CD16+56 and CD68) of blister fluid cells were measured by flow cytometry.

Results: The concentrations of all cytokines in the serum and blister fluid were higher than those in the controls and were more elevated in the blister fluid than in the serum. Moreover, sTRAIL, IFN-γ and TNF-α quantities were relatively stable, while those of sFasL and granulysin decreased rapidly in the disease course. On the first day, CD8+ T and natural killer cells were predominant in the blister fluid but their relative percentage diminished gradually, while that of CD14+ cells increased.

Conclusion: Our study confirmed there are high but variable levels of these cytokines in SJS/TEN, especially in the early phase and different tendencies are manifested in the disease course.

Keywords: Stevens-Johnson syndrome; apoptosis; keratinocyte; toxic epidermal necrolysis.

MeSH terms

  • Adult
  • Antigens, Differentiation / metabolism*
  • Apoptosis*
  • Blister / metabolism*
  • Case-Control Studies
  • Cytokines / blood*
  • Cytokines / metabolism
  • Female
  • Humans
  • Male
  • Middle Aged
  • Signal Transduction
  • Stevens-Johnson Syndrome / blood*
  • Stevens-Johnson Syndrome / metabolism
  • Young Adult

Substances

  • Antigens, Differentiation
  • Cytokines