A coding polymorphism in the CYSLT2 receptor with reduced affinity to LTD4 is associated with asthma

Sreekumar G. Pillai, Diane J. Cousens, Ashley A. Barnes, Peter T. Buckley, Mathias N. Chiano, Louise K. Hosking, Lee Ann Cameron, Mary E. Fling, James J. Foley, Andrew Green, Henry M. Sarau, Dulcie B. Schmidt, Catherine S. Sprankle, Malcolm N. Blumenthal, Jorgen Vestbo, Karen Kennedy-Wilson, William E. Wixted, Michael J. Wagner, Wayne H. Anderson, Diane M. IgnarPeter Helms, Karin Carlsen, John Tsanakas, Warren Lenney, Moira Whyte, Peter Sly, Michael Silverman, John Sundy, Kathleen Barnes, Jorrit Gerritsen, Andrea Von Berg

    Research output: Contribution to journalArticlepeer-review


    Background: Cysteinyl leukotrienes (CYSLTR) are potent biological mediators in the pathophysiology of asthma for which two receptors have been characterized, CYSLTR1 and CYSLTR2. The leukotriene modifying agents currently used to control bronchoconstriction and inflammation in asthmatic patients are CYSLTR1-specific leukotriene receptor antagonists. In this report, we investigated a possible role for therapeutic modulation of CYSLTR2 in asthma by investigating genetic association with asthma and further characterization of the pharmacology of a coding polymorphism. Methods: The association of CYSLTR2 polymorphisms with asthma was assessed by transmission disequilibrium test in two family-based collections (359 families from Denmark and Minnesota, USA and 384 families from the Genetics of Asthma International Newtwork). Results: A significant association of the coding polymorphism, 601A>G, with asthma was observed (P = 0.003). We replicated these findings in a collection of 384 families from the Genetics of Asthma International Network (P = 0.04). The G allele is significantly under-transmitted to asthmatics, indicating a possible role for this receptor in resistance to asthma. The potency of cysteinyl leukotrienes at the wild-type CYSLTR2 and the coding polymorphism 601A>G were assessed using a calcium mobilization assay. The potency of LTC4 and LTE4 was similar for both forms of the receptor and LTB4 was inactive, however, LTD4 was approximately five-fold less potent on 601A>G compared to wild-type CYSLTR2. Conclusions: Since 601A>G alters the potency of LTD4 and this variant allele may be associated with resistance to asthma, it is possible that modulation of the CYSLTR2 may be useful in asthma pharmacotherapy. © 2004 Lippincott Williams & Wilkins.
    Original languageEnglish
    Pages (from-to)627-633
    Number of pages6
    Issue number9
    Publication statusPublished - Sept 2004


    • Association
    • Asthma
    • Cysteinyl leukotrienes
    • Polymorphism
    • Transmission disequilibrium test


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