Ohashi Y, Nakai Y, Sakamoto H, Ohno Y, Sugiura Y, Okamoto H, Tanaka A, Kakinoki Y, Kishimoto K, Hayashi M
Department of Otolaryngology, Osaka City University Medical School, Japan.
Ann Allergy Asthma Immunol. 1996 Sep;77(3):203-8. doi: 10.1016/S1081-1206(10)63256-5.
Interleukin-2 receptor (IL-2R) exists in soluble form in sera, and the rate of release of the soluble form of IL-2R (soluble IL-2R) reflects T cell activation in vivo. Since T lymphocytes play a central role in respiratory allergic disorders, the measurement of serum levels of soluble IL-2R may be useful in analyzing the disease state of allergic disorders.
To investigate the serum concentrations of soluble IL-2R in 48 patients with perennial allergic rhinitis and 14 nonatopic healthy controls, with special reference to the possible changes following long-term immunotherapy.
This retrospective study included 48 patients who had had variable periods of long-term immunotherapy with Dermatophagoides farinae extracts. The duration of immunotherapy ranged from 5 to 15 years. Serum samples were collected twice from each patient, before the initiation of immunotherapy and at the time of clinical assessment of immunotherapy. All the serum samples were simultaneously used for determination of soluble IL-2R concentrations, by the use of an enzyme-linked immunosorbent assay. To serve as controls, 14 nonallergic subjects of the same age range and sex were chosen.
Patients with allergic rhinitis before immunotherapy had significantly higher serum levels of soluble IL-2R than nonatopic subjects. Elevated serum levels of soluble IL-2R decreased significantly following immunotherapy and the serum levels of soluble IL-2R in patients with allergic rhinitis after immunotherapy were not statistically different from those of nonatopic subjects. In addition, the percent decrease in serum soluble IL-2R correlated significantly with the duration of immunotherapy.
Hyperactivity of helper T cells of atopic patients is altered after long-term immunotherapy, and such immunoregulatory changes could be theoretically involved in the mechanisms of immunotherapy.
白细胞介素-2受体(IL-2R)以可溶性形式存在于血清中,可溶性IL-2R(sIL-2R)的释放速率反映体内T细胞的激活情况。由于T淋巴细胞在呼吸道过敏性疾病中起核心作用,测定血清sIL-2R水平可能有助于分析过敏性疾病的病情。
研究48例常年性变应性鼻炎患者和14例非特应性健康对照者血清sIL-2R的浓度,特别关注长期免疫治疗后可能出现的变化。
这项回顾性研究纳入了48例接受不同疗程粉尘螨提取物长期免疫治疗的患者。免疫治疗持续时间为5至15年。从每位患者身上采集两次血清样本,一次在免疫治疗开始前,另一次在免疫治疗临床评估时。所有血清样本同时用于通过酶联免疫吸附测定法测定sIL-2R浓度。选择14例年龄范围和性别相同的非过敏受试者作为对照。
免疫治疗前变应性鼻炎患者血清sIL-2R水平显著高于非特应性受试者。免疫治疗后血清sIL-2R升高水平显著下降,免疫治疗后变应性鼻炎患者血清sIL-2R水平与非特应性受试者无统计学差异。此外,血清可溶性IL-2R下降百分比与免疫治疗持续时间显著相关。
特应性患者辅助性T细胞的高活性在长期免疫治疗后发生改变,这种免疫调节变化理论上可能参与免疫治疗机制。