Jerzyńska Joanna, Stelmach Włodzimierz, Majak Pawel, Brzozowska Agnieszka, Sobocińska Agnieszka, Stelmach Iwona
Department of Pediatrics and Allergy, Medical University of Lodz, Poland.
Allergy Asthma Proc. 2008 May-Jun;29(3):274-9. doi: 10.2500/aap.2008.29.3112.
There is no general agreement among investigators regarding the effect of specific immunotherapy (SIT) on T-cell reactivity. The aim of this study was to investigate the serum levels of IL-1beta, IL-6, and TNF-alpha of children with allergic asthma before and after 3 and 12 months of SIT. Additionally, after 12 months of SIT, we investigated the bronchial hyperresponsiveness. The secondary end points were clinical parameters. Thirty-two children with moderate asthma allergic to house-dust mites (study group) and 10 healthy children (control group) participated in this trial. At each visit blood samples were drawn from all asthmatic patients and at the prestudy visit in controls for determination of parameters. All asthmatic patients received SIT. At the second study visit, baseline spirometry and methacholine challenge tests were performed. Serum TNF-alpha during SIT tended to increase after 3 months with respect to baseline, whereas after 12 months of SIT, serum TNF-alpha decreased. The correlation coefficient (r) between the changes in TNF-alpha values between 3 and 12 months of SIT and provocative concentrations of methacholine to cause a 20% fall in FEV(1) (PC20M) after 12 months of SIT was positive (r = 0.76; p < 0.0001); the greater the changes in TNF-alpha level, the higher the PC20. No modification of IL-1beta and IL-6 was observed. Clinical symptoms also improved after 12 months of SIT in children with asthma. In summary, our results showed the variations in serum levels of TNF-alpha during SIT in asthmatic children and confirm anti-inflammatory properties of SIT.
关于特异性免疫疗法(SIT)对T细胞反应性的影响,研究者之间尚未达成普遍共识。本研究的目的是调查过敏性哮喘患儿在SIT治疗3个月和12个月前后血清白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)和肿瘤坏死因子-α(TNF-α)的水平。此外,在SIT治疗12个月后,我们调查了支气管高反应性。次要终点为临床参数。32名对屋尘螨过敏的中度哮喘患儿(研究组)和10名健康儿童(对照组)参与了本试验。每次就诊时均采集所有哮喘患者的血样,并在对照组研究前就诊时采集血样以测定参数。所有哮喘患者均接受SIT治疗。在第二次研究就诊时,进行了基线肺活量测定和乙酰甲胆碱激发试验。SIT治疗3个月后,血清TNF-α相对于基线水平有升高趋势,而在SIT治疗12个月后,血清TNF-α降低。SIT治疗3个月至12个月期间TNF-α值的变化与SIT治疗12个月后使第一秒用力呼气容积(FEV₁)下降20%的乙酰甲胆碱激发浓度(PC20M)之间的相关系数(r)为正(r = 0.76;p < 0.0001);TNF-α水平变化越大,PC20越高。未观察到IL-1β和IL-6的改变。哮喘患儿在SIT治疗12个月后临床症状也有所改善。总之,我们的结果显示了哮喘患儿在SIT治疗期间血清TNF-α水平的变化,并证实了SIT的抗炎特性。