Malaghan Institute of Medical Research, Wellington, New Zealand.
Eur J Immunol. 2014 Jul;44(7):1976-80. doi: 10.1002/eji.201344400. Epub 2014 May 19.
A keenly sought therapeutic approach for the treatment of allergic disease is the identification and neutralization of the cytokine that regulates the differentiation of T helper 2 (Th2) cells. Th2 cells are exciting targets for asthma therapies. Recently, the cytokine IL-25 has been shown to enhance Th2-type immune activity and play important roles in mediating allergic inflammatory responses. To investigate this further, we crossed IL-25(-/-) C57BL/6 mice with G4 IL-4 C57BL/6 reporter mice and developed an assay for in vitro and in vivo IL-4-independent Th2-cell differentiation. These assays were used to determine whether IL-25 was critical for the formation of Th2 cells. We found there was no physiological role for IL-25 in either the differentiation of Th2 cells or their development to effector or memory Th2-cell subsets. Importantly, this data challenges the newly found and growing status of the cytokine IL-25 and its proposed role in promoting Th2-cell responses.
一种备受关注的治疗过敏疾病的方法是鉴定和中和调节 T 辅助细胞 2(Th2)细胞分化的细胞因子。Th2 细胞是哮喘治疗的理想靶点。最近,细胞因子 IL-25 已被证明可以增强 Th2 型免疫活性,并在介导过敏炎症反应中发挥重要作用。为了进一步研究这一点,我们将 IL-25(-/-) C57BL/6 小鼠与 G4 IL-4 C57BL/6 报告小鼠杂交,并开发了一种用于体外和体内 IL-4 非依赖性 Th2 细胞分化的测定方法。这些测定用于确定 IL-25 是否对 Th2 细胞的形成至关重要。我们发现 IL-25 在 Th2 细胞的分化或其向效应或记忆 Th2 细胞亚群的发育中没有生理作用。重要的是,这一数据挑战了新发现的细胞因子 IL-25 的不断增长的地位及其在促进 Th2 细胞反应中的作用。