Do Genetic Mutations and Genotypes Contribute to Onychomycosis?

被引:15
作者
Gupta, Aditya K. [1 ,2 ]
Simpson, Fiona C. [2 ]
Brintnell, William C. [2 ]
机构
[1] Univ Toronto, Dept Med, Div Dermatol, Toronto, ON, Canada
[2] Mediprobe Res Inc, London, ON, Canada
关键词
Genetic mutations; Genotypes; Genetic susceptibility; Onychomycosis; TOENAIL ONYCHOMYCOSIS; SUSCEPTIBILITY; DERMATOPHYTES; EPIDEMIOLOGY; PREVALENCE; NAIL; RECOGNITION; DEFICIENCY; STRATEGIES; PATTERN;
D O I
10.1159/000358586
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: The variability in susceptibility to onychomycosis for individuals exposed to the same environmental risk factors raises the possibility that there may be individuals with a genetic predisposition to dermatophyte infection. Objective: To determine whether there are genetic mutations or genotypes which contribute to onychomycosis. Methods:The PubMed database was searched for examples of immune deficiencies resulting in dermatophyte infections. Results:There are mutations in the innate immune receptors Dectin-1 and its adaptor protein CARD9 which result in familial mucocutaneous infections. There are also specific human leukocyte antigen genotypes that are more common in individuals and families with a high prevalence of onychomycosis. In addition, some patients have been reported with insufficient levels of CD4+CD25+ regulatory T cells. These deficits impair a full innate and adaptive immune response and may result in chronic or recurrent infections. Conclusions:There are documented mutations and genotypes that contribute to familial and individual susceptibility to onychomycosis. (C) 2014 S. Karger AG, Basel
引用
收藏
页码:207 / 210
页数:4
相关论文
共 32 条
  • [31] HLA-Associated susceptibility to chronic onychomycosis in Brazilian Ashkenazic Jews
    Zaitz, C
    Campbell, I
    Moraes, JR
    Moraes, ME
    Gouvea, C
    Romero, M
    Gouvea, N
    Sadahiro, A
    Chamone, D
    Dorlhiac, P
    [J]. INTERNATIONAL JOURNAL OF DERMATOLOGY, 1996, 35 (09) : 681 - 682
  • [32] Familial chronic nail candidiasis with ICAM-1 deficiency: a new form of chronic mucocutaneous candidiasis
    Zuccarello, D
    Salpietro, DC
    Gangemi, S
    Toscano, V
    Merlino, MV
    Briuglia, S
    Bisignano, G
    Mangino, M
    Mingarelli, R
    Dallapiccola, B
    [J]. JOURNAL OF MEDICAL GENETICS, 2002, 39 (09) : 671 - 675