Literature DB >> 11544479

Gene polymorphism in Netherton and common atopic disease.

A J Walley1, S Chavanas, M F Moffatt, R M Esnouf, B Ubhi, R Lawrence, K Wong, G R Abecasis, E Y Jones, J I Harper, A Hovnanian, W O Cookson.   

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.

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Year:  2001        PMID: 11544479     DOI: 10.1038/ng728

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  82 in total

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