Abstract

Mast cells (MCs) play a central role in the development of IgE-mediated allergic diseases, including allergic urticaria and food allergy. SCF/KIT signaling is essential for the differentiation, proliferation, survival, and activation of MCs. Thus, highly selective KIT inhibitors would have therapeutic potential for IgE/mast cell-mediated allergic diseases through homeostatic regulation of mast cells while minimizing side effects caused by the inhibition of non-KIT kinases, such as PDGFR and VEGFR.

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