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Interleukin-5–producing group 2 innate lymphoid cells control eosinophilia induced by interleukin-2 therapy

机译:产生白细胞介素5的第2组先天淋巴样细胞控制由白细胞介素2治疗引起的嗜酸性粒细胞增多

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摘要

Interleukin (IL)-2 promotes regulatory T-cell development and function, and treatment with IL-2 is being tested as therapy for some autoimmune diseases. However, patients receiving IL-2 treatment also experience eosinophilia due to an unknown mechanism. Here, we show that patients receiving low-dose IL-2 have elevated levels of serum IL-5, and this correlates with their degree of eosinophilia. In mice, low-dose IL-2–anti-IL-2 antibody complexes drove group 2 innate lymphoid cells (ILC2) to produce IL-5 and proliferate. Using genetic approaches in mice, we demonstrate that activation of ILC2 was responsible for the eosinophilia observed with IL-2 therapy. These observations reveal a novel cellular network that is activated during IL-2 treatment. A better understanding of the cross talk between these cell populations may lead to more effective targeting of IL-2 to treat autoimmune disease.
机译:白介素(IL)-2促进调节性T细胞的发育和功能,目前正在测试用IL-2作为某些自身免疫性疾病的治疗方法。但是,由于未知的机制,接受IL-2治疗的患者也会出现嗜酸性粒细胞增多。在这里,我们显示接受低剂量IL-2的患者血清IL-5水平升高,这与他们的嗜酸性粒细胞增多程度相关。在小鼠中,低剂量的IL-2-抗IL-2抗体复合物驱使第2组先天性淋巴样细胞(ILC2)产生IL-5并增殖。使用小鼠中的遗传学方法,我们证明了IL-2的激活是IL-2治疗观察到的嗜酸性粒细胞的原因。这些观察结果揭示了在IL-2治疗期间被激活的新型细胞网络。更好地了解这些细胞群之间的串扰可能会导致更有效地靶向IL-2来治疗自身免疫性疾病。

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