“…In the presence of interleukin-3 (IL-3) -secreting T cells rodent mast cell progenitors undergo proliferation and specific differentiation toward the mucosal phenotype [1][2][3][4][5], which is considered a major mechanism of defense during parasite infestation [6][7][8][9][10]. On the other hand, it is well established that both rodent and human mast cells are one main source for several cytokines [tumor necrosis factor ␣ (TNF-␣), IL-3, IL-4, IL-5, IL-6, IL-8, IL-13] [11][12][13][14][15][16][17][18][19] and growth factors [20,21] that can regulate directly or indirectly, the development, phenotype, and function of T [22][23][24][25][26][27][28] and B cells [21]. Subsequently, mast cells and T cells seem to complement the functions of each other, thus contributing to the cytokine pool that leads to chronic inflammation.…”