“…For example, eosinophil‐derived TGF‐β is linked to tissue remodeling and induction of the extracellular matrix protein periostin in patient biopsy specimens which increases eosinophil infiltration in the mucosal layer, thus facilitating disease pathogenesis 26, 27. Furthermore, as indicated above, granule proteins such as eosinophil cationic protein, Epx, and major basic protein released by activated eosinophils during inflammation can contribute to tissue damage (alter barrier function) and dysfunction (diarrhea with bleeding) 9, 10, 11, 12. Deficiency of eotaxin‐1, the eosinophil‐specific chemokine, or blockade of its receptor (CCR3) resulting in depletion of eosinophils has been shown to attenuate inflammation in experimental models of IBD,9, 28 thus supporting the overall importance of eosinophil involvement in EGID.…”