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Editorial
. 2012 Jan;12(1):3.
doi: 10.1111/j.1600-6143.2011.03937.x.

Literature watch implications for transplantation. The anti-infectious role of the IL-17 pathway

Editorial

Literature watch implications for transplantation. The anti-infectious role of the IL-17 pathway

Maria-Luisa Alegre et al. Am J Transplant. 2012 Jan.
No abstract available

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Figures

Figure 1
Figure 1. Proposed model of how genetic mutations affect the Th17 pathway
The authors have identified a gain-of-function mutation in STAT1 that antagonizes STAT3-mediated Th17 differentiation (1.), a loss-of-function mutation in IL-17F (2.), a mutation in AIRE resulting in neutralizing anti-IL-17 antibodies (3.) and a loss-of-function mutation in the receptor for IL-17A/F (4.) that are all associated with CMC.

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References

    1. Puel A, Cypowyj S, Bustamante J, Wright JF, Liu L, Lim HK, et al. Chronic mucocutaneous candidiasis in humans with inborn errors of interleukin-17 immunity. Science. 2011;332(6025):65–68. - PMC - PubMed
    1. Liu L, Okada S, Kong XF, Kreins AY, Cypowyj S, Abhyankar A, et al. Gain-of-function human STAT1 mutations impair IL-17 immunity and underlie chronic mucocutaneous candidiasis. The Journal of experimental medicine. 2011;208(8):1635–1648. - PMC - PubMed
    1. Puel A, Doffinger R, Natividad A, Chrabieh M, Barcenas-Morales G, Picard C, et al. Autoantibodies against IL-17A, IL-17F, and IL-22 in patients with chronic mucocutaneous candidiasis and autoimmune polyendocrine syndrome type I. The Journal of experimental medicine. 2010;207(2):291–297. - PMC - PubMed

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