No remarkable differences in rates of sensitization to common type I and IV allergens between FLG loss-of-function mutation carriers and wild-type subjects

Contact Dermatitis. 2014 Jan;70(1):27-34. doi: 10.1111/cod.12109. Epub 2013 Jul 15.

Abstract

Background: Loss-of-function mutations in the filaggrin gene (FLG) have been associated with reduced skin barrier function, possibly allowing increased penetration of irritants and allergens.

Objectives: To study whether FLG loss-of-function mutation carriers show different rates of sensitization to common type I and IV allergens among patients referred for occupational contact dermatitis of the hands.

Materials and methods: Four hundred and ninety-six Caucasian patients were genotyped for four FLG null mutations and patch tested with the European baseline series. In addition, 431 patients underwent prick testing with common type I allergens.

Results: Overall, 67 patients showed a heterozygous mutation in the FLG alleles R501X, R2447X, S3247X, and/or 2282del4. Sensitization rates for type I allergens from a European prick test series did not show significant differences between FLG loss-of-function mutation carriers and wild-type subjects. For type IV allergens, significantly more FLG loss-of-function carriers were found to be sensitized to lanolin and p-tert-butylphenol-formaldehyde resin.

Conclusions: Probably a variety of immunological mechanisms other than that resulting from the filaggrin system have an impact on allergic sensitization to a greater degree. Larger cohorts may be necessary to increase the statistical power of the findings presented regarding type I and IV sensitization.

Keywords: allergens; contact dermatitis; filaggrin gene; loss-of-function mutations; patch test; prick test.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Allergens / genetics*
  • Allergens / immunology
  • Cohort Studies
  • Dermatitis, Allergic Contact / diagnosis
  • Dermatitis, Allergic Contact / genetics*
  • Dermatitis, Allergic Contact / immunology
  • Dermatitis, Occupational / diagnosis
  • Dermatitis, Occupational / genetics*
  • Dermatitis, Occupational / immunology
  • Female
  • Filaggrin Proteins
  • Genetic Markers
  • Genetic Predisposition to Disease
  • Genotyping Techniques
  • Hand
  • Heterozygote
  • Humans
  • Intermediate Filament Proteins / deficiency
  • Intermediate Filament Proteins / genetics*
  • Logistic Models
  • Male
  • Middle Aged
  • Mutation
  • Skin Tests
  • Young Adult

Substances

  • Allergens
  • FLG protein, human
  • Filaggrin Proteins
  • Genetic Markers
  • Intermediate Filament Proteins