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Gene polymorphism in Netherton and common atopic disease.

Authors :
Walley AJ
Chavanas S
Moffatt MF
Esnouf RM
Ubhi B
Lawrence R
Wong K
Abecasis GR
Jones EY
Harper JI
Hovnanian A
Cookson WO
Source :
Nature genetics [Nat Genet] 2001 Oct; Vol. 29 (2), pp. 175-8.
Publication Year :
2001

Abstract

Atopic dermatitis (AD) and asthma are characterized by IgE-mediated atopic (allergic) responses to common proteins (allergens), many of which are proteinases. Loci influencing atopy have been localized to a number of chromosomal regions, including the chromosome 5q31 cytokine cluster. Netherton disease is a rare recessive skin disorder in which atopy is a universal accompaniment. The gene underlying Netherton disease (SPINK5) encodes a 15-domain serine proteinase inhibitor (LEKTI) which is expressed in epithelial and mucosal surfaces and in the thymus. We have identified six coding polymorphisms in SPINK5 (Table 1) and found that a Glu420-->Lys variant shows significant association with atopy and AD in two independent panels of families. Our results implicate a previously unrecognized pathway for the development of common allergic illnesses.

Details

Language :
English
ISSN :
1061-4036
Volume :
29
Issue :
2
Database :
MEDLINE
Journal :
Nature genetics
Publication Type :
Academic Journal
Accession number :
11544479
Full Text :
https://doi.org/10.1038/ng728