Article

Activation of T-cells from allergic patients and volunteers by p-phenylenediamine and Bandrowski's base.

Department of Pharmacology, The University of Liverpool, Liverpool, UK.
Journal of Investigative Dermatology (impact factor: 6.31). 05/2008; 128(4):897-905. DOI:10.1038/sj.jid.5701071 pp.897-905
Source: PubMed

ABSTRACT Allergic contact dermatitis is commonly associated with exposure to p-phenylenediamine. The aim of this study was to determine whether p-phenylenediamine (PPD) and/or Bandrowski's base (BB) stimulate T cells from allergic patients and volunteers, and to explore the relationship between T-cell immunogenicity and allergy. Lymphocytes from allergic patients proliferated with PPD and BB (n=8). Lymphocytes from 14/16 non-allergic individuals also proliferated following stimulation, but only with BB; cord blood lymphocytes failed to respond (n=6). Glutathione, which prevented BB formation, but not binding of PPD to cells and serum, did not prevent p-phenylenediamine-specific stimulation of patient lymphocytes. T-cell clones generated from allergic patients were stimulated separately with PPD and BB, while clones from volunteers proliferated with BB alone. Patient and volunteer clones secreted IL-4, IL-5, IL-13, TNF-alpha, MIP-1alpha, MIP-1beta, and RANTES. These data show that activation of T lymphocytes from allergic individuals alone with PPD represents an important discrimination between allergic and non-allergic groups. BB-specific T cells are found in both allergic patients and volunteers, but not in cord blood. Their presence seems to reflect an acquired immune response, which is not translated into an allergic reaction.

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Keywords

14/16 non-allergic individuals
 
acquired immune response
 
allergic
 
Allergic contact dermatitis
 
allergic individuals
 
allergic patients
 
allergic patients proliferated
 
allergic reaction
 
Bandrowski's base
 
BB-specific T cells
 
cord blood lymphocytes
 
non-allergic groups
 
p-phenylenediamine-specific stimulation
 
patient lymphocytes
 
prevented BB formation
 
T lymphocytes
 
T-cell clones
 
T-cell immunogenicity
 
volunteer clones secreted IL-4
 
volunteers proliferated