Measurement of CD4 and CD8 T-lymphocyte cytokine secretion and gene expression changes in p-phenylenediamine allergic patients and tolerant individuals

Eve M. Coulter, Claire Jenkinson, John Farrell, Sidonie N. Lavergne, Camilla Pease, Andrew White, Maja Aleksic, David Basketter, Dominic P. Williams, Clodagh King, Munir Pirmohamed, B. Kevin Park, Dean J. Naisbitt

Research output: Contribution to journalArticlepeer-review

Abstract

Factors predisposing to individual susceptibility to contact allergic dermatitis are ill defined. This study was designed to characterize the response of allergic and tolerant individuals T-lymphocytes after exposure to p-phenylenediamine (PPD). Peripheral blood mononuclear cells (PBMCs) from allergic patients proliferated when treated with PPD and Bandrowski's base (BB) and secreted IL-1α,-1Β,-4,-5,-6,-8,-10, and-13; IFN-γ; tumor necrosis factor-α; MIP-1α/Β; MCP-1 (monocyte chemotactic protein-1); and RANTES. PBMCs from tolerant individuals were stimulated to proliferate only with BB, and they secreted significantly lower levels of Th2 cytokines. Principal component analysis showed that genes are differentially expressed between the patient groups. A network-based analysis of microarray data showed upregulation of T helper type 2 (Th2) gene pathways, including IL-9, in allergic patients, but a regulatory gene profile in tolerant individuals. Real-time PCR confirmed the observed increase in Th2 cytokine gene transcription in allergic patients. Purified CD4 and CD8 T cells from allergic patients were stimulated to proliferate and secrete Th2 cytokines following antigen exposure. Only CD4 T cells from tolerant individuals were stimulated by BB, and levels of Th2 cytokines were 80% lower. The nature of the antigenic determinant stimulating PBMCs and levels of Th2 cytokines, including IL-9, was confirmed in a validation cohort. These studies show increased activity of Th2 cytokines in CD4 and CD8 T cells from individuals with allergic contact dermatitis.

Original languageEnglish (US)
Pages (from-to)161-174
Number of pages14
JournalJournal of Investigative Dermatology
Volume130
Issue number1
DOIs
StatePublished - Jan 2010

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Dermatology
  • Cell Biology

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