Dermal Periostin: A New Player in Itch of Prurigo Nodularis

Authors

  • Takashi Hashimoto
  • Leigh A. Nattkemper
  • Hei Sung Kim
  • Christina D. Kursewicz
  • Emilie Fowler
  • Serena M. Shah
  • Sonali Nanda
  • Rachel A. Fayne
  • Paolo Romanelli
  • Gil Yosipovitch Dr. Phillip Frost Department of Dermatology & Cutaneous Surgery, University of Miami Miller School of Medicine, 33136 Miami, FL, USA

DOI:

https://doi.org/10.2340/00015555-3702

Abstract

Abstract is missing (Short communication)

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References

Pereira MP, Hoffmann V, Weisshaar E, Wallengren J, Halvorsen JA, Garcovich S, et al. Chronic nodular prurigo: clinical profile and burden. A European cross-sectional study. J Eur Acad Dermatol Venereol 2020; 34: 2373-2383.

DOI: https://doi.org/10.1111/jdv.16309

Yosipovitch G. Prurigo nodularis: New treatments on the horizon. J Am Acad Dermatol 2020; 82: 1035-1036.

DOI: https://doi.org/10.1016/j.jaad.2019.02.061

Sonkoly E, Muller A, Lauerma AI, Pivarcsi A, Soto H, Kemeny L, et al. IL-31: A new link between T cells and pruritus in atopic skin inflammation. J Allergy Clin Immunol 2006; 117: 411-417.

DOI: https://doi.org/10.1016/j.jaci.2005.10.033

Zhong W, Wu X, Zhang W, Zhang J, Chen X, Chen S, et al. Aberrant expression of histamine-independent pruritogenic mediators in keratinocytes may be involved in the pathogenesis of prurigo nodularis. Acta Derm Venereol 2019; 99: 579-586.

DOI: https://doi.org/10.2340/00015555-3150

Mishra SK, Wheeler JJ, Pitake S, Ding H, Jiang C, Fukuyama T, et al. Periostin activation of integrin receptors on sensory neurons induces allergic itch. Cell Reports 2020; 31: 107472.

DOI: https://doi.org/10.1016/j.celrep.2020.03.036

Sanders KM, Nattkemper LA, Rosen JD, Andersen HH, Hsiang J, Romanelli P, et al. Non-histaminergic itch mediators elevated in the skin of a porcine model of scabies and of human scabies patients. J Invest Dermatol 2019; 139: 971-973.

DOI: https://doi.org/10.1016/j.jid.2018.09.032

Kanda Y. Investigation of the freely available easy-to-use software "EZR" for medical statistics. Bone Marrow Transpl 2013; 48: 452-458.

DOI: https://doi.org/10.1038/bmt.2012.244

Masuoka M, Shiraishi H, Ohta S, Suzuki S, Arima K, Aoki S, et al. Periostin promotes chronic allergic inflammation in response to Th2 cytokines. J Clin Invest 2012; 122: 2590-2600.

DOI: https://doi.org/10.1172/JCI58978

Hashimoto T, Satoh T, Yokozeki H. Pruritus in ordinary scabies: IL-31 from macrophages induced by overexpression of thymic stromal lymphopoietin and periostin. Allergy 2019; 74: 1727-1737.

DOI: https://doi.org/10.1111/all.13870

Hashimoto T, Kursewicz CD, Fayne RA, Nanda S, Shah SM, Nattkemper L, et al. Mechanisms of itch in stasis dermatitis: Significant role of IL-31 from macrophages. J Invest Dermatol 2020; 140: 850-859.

DOI: https://doi.org/10.1016/j.jid.2019.09.012

Hashimoto T, Kursewicz CD, Fayne RA, Nanda S, Shah SM, Nattkemper L, et al. Pathophysiological mechanisms of itch in bullous pemphigoid. J Am Acad Dermatol 2020; 83: 53-62.

DOI: https://doi.org/10.1016/j.jaad.2019.07.060

Park K, Mori T, Nakamura M, Tokura Y. Increased expression of mRNAs for IL-4, IL-17, IL-22 and IL-31 in skin lesions of subacute and chronic forms of prurigo. Eur J Dermatol 2011; 21: 135-136.

DOI: https://doi.org/10.1684/ejd.2010.1196

Shiraishi H, Masuoka M, Ohta S, Suzuki S, Arima K, Taniguchi K, et al. Periostin contributes to the pathogenesis of atopic dermatitis by inducing TSLP production from keratinocytes. Allergy Int 2012; 61: 563-572.

DOI: https://doi.org/10.2332/allergolint.10-OA-0297

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Published

2021-01-20

How to Cite

Hashimoto, T., Nattkemper, L. A., Kim, H. S., Kursewicz, C. D., Fowler, E., Shah, S. M., … Yosipovitch, G. (2021). Dermal Periostin: A New Player in Itch of Prurigo Nodularis. Acta Dermato-Venereologica, 101(1), adv00375. https://doi.org/10.2340/00015555-3702

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