From the *Department of Allergy and Immunology, National Research Institute for Child Health and Development; the †Atopy Research Center, Juntendo University; and the ‡Department of Otolaryngology, Division of Rhinology and Allergy, Nippon Medical School, Tokyo, Japan.
World Allergy Organ J. 2008 Jan;1(1):9-14. doi: 10.1097/wox.0b013e3181629ae3.
Regulatory T (Treg) cells are considered to inhibit the development of both type 1 (Th1) and type 2 helper T (Th2) cells. However, it is recently reported that there are reduced numbers of Treg cells in patients with allergic diseases as compared with individuals who have high levels of serum immunoglobulin E and blood eosinophils but are asymptomatic. Therefore, Treg cells may suppress the onset of allergic disease by down-regulating other types of immune cells besides Th1 and Th2 cells. The newly discovered interleukin 17-producing helper T cells that are responsible for autoimmune inflammatory diseases may counteract Treg cells even in allergic diseases. The Th2 cells that are capable of producing of high levels of tumor necrosis factor-α may also be involved in inflammation in allergic diseases. In this review, we further discuss the role of Th1, Th2, interleukin 17-producing helper T cells, and Treg cells in allergic diseases by using the balancing square model and the factors differentiating between patients with clinical manifestations of allergic symptomatic and atopic individuals who are sensitized but asymptomatic.
调节性 T(Treg)细胞被认为可以抑制 1 型(Th1)和 2 型辅助 T(Th2)细胞的发展。然而,最近有报道称,与高血清免疫球蛋白 E 和血嗜酸性粒细胞但无症状的个体相比,过敏性疾病患者的 Treg 细胞数量减少。因此,Treg 细胞可能通过下调除 Th1 和 Th2 细胞以外的其他类型免疫细胞来抑制过敏性疾病的发生。新发现的产生白细胞介素 17 的辅助 T 细胞负责自身免疫性炎症性疾病,即使在过敏性疾病中也可能与 Treg 细胞对抗。能够产生高水平肿瘤坏死因子-α的 Th2 细胞也可能参与过敏性疾病的炎症反应。在这篇综述中,我们进一步讨论了 Th1、Th2、产生白细胞介素 17 的辅助 T 细胞和 Treg 细胞在过敏性疾病中的作用,使用了平衡方模型和区分有临床表现的过敏症状患者和致敏但无症状的特应性个体的因素。