Basophil-derived amphiregulin is essential for UVB irradiation-induced immune suppression

Meulenbroeks C, Van Weelden H, Schwartz C, Vöhringer D, Redegeld FAM, Rutten VPMG, Willemse T, Sijts AJAM, Zaiss DMW (2015)


Publication Type: Journal article

Publication year: 2015

Journal

Book Volume: 135

Pages Range: 222-8

Journal Issue: 1

DOI: 10.1038/jid.2014.329

Abstract

UVB irradiation (290-320 nm) is used to treat skin diseases like psoriasis and atopic dermatitis, and is known to suppress contact hypersensitivity (CHS) reactions in mouse models. Regulatory T cells (Treg cells) have been shown to be responsible for this UVB-induced suppression of CHS. The epidermal growth factor (EGF)-like growth factor amphiregulin (AREG) engages EGFR on Treg cells and, in different disease models, it was shown that mast cell-derived AREG is essential for optimal Treg cell function in vivo. Here we determined whether AREG has a role in UVB-induced, Treg cell-mediated suppression of CHS reactions in the skin. Our data show that AREG is essential for UVB-induced CHS suppression. In contrast to the general assumption, however, mast cells were dispensable for UVB-induced immune suppression, whereas basophil-derived AREG was essential. These data reveal, to our knowledge, a previously unreported function for basophils in the homeostasis of immune responses in the skin. Basophils thus fulfill a dual function: they contribute to the initiation of effective type 2 immune responses and, by enhancing the suppressive capacity of local Treg cell populations, also to local immune regulation in the skin.

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APA:

Meulenbroeks, C., Van Weelden, H., Schwartz, C., Vöhringer, D., Redegeld, F.A.M., Rutten, V.P.M.G.,... Zaiss, D.M.W. (2015). Basophil-derived amphiregulin is essential for UVB irradiation-induced immune suppression. Journal of Investigative Dermatology, 135(1), 222-8. https://doi.org/10.1038/jid.2014.329

MLA:

Meulenbroeks, Chantal, et al. "Basophil-derived amphiregulin is essential for UVB irradiation-induced immune suppression." Journal of Investigative Dermatology 135.1 (2015): 222-8.

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