Renzi P M, Turgeon J P, Yang J P, Drblik S P, Marcotte J E, Pedneault L, Spier S
Sainte-Justine, Research Center, University of Montreal, Quebec, Canada.
J Pediatr. 1997 Apr;130(4):584-93. doi: 10.1016/s0022-3476(97)70243-9.
To determine whether abnormalities of cellular immunity are present and linked to early wheezing after bronchiolitis.
We prospectively studied 26 infants hospitalized for a first episode of bronchiolitis and without any prior immune, cardiac, or respiratory disease. Blood was obtained at the time of enrollment and 5 months later for the assessment of the total cellular and differential counts, CD4+ (helper) and CD8+ (suppressor/cytotoxic) lymphocytes, and the activation markers CD23 (low-affinity immunoglobulin E receptor) and CD25 (interleukin-2 (IL-2) receptor). The cytokines interferon gamma (T-helper (TH) type-1 cytokine) and IL-4 (TH-2) were measured in plasma and in vitro after stimulation with IL-2 or with the house-dust mite (Dermatophagoides farinae) antigen. A daily log of episodes of wheezing was kept by parents after discharge.
We found an increase in blood eosinophils, an increased percentage of CD4+, CD25+, and CD23+ lymphocytes in subjects at 5 months compared with the time of bronchiolitis and with healthy subjects of the same age (p < 0.05). Plasma IL-4 levels, although not different from those of healthy subjects, also increased significantly. Peripheral blood lymphocytes from infants who wheezed produced more IL-4 in vitro, 5 months after bronchiolitis, in response to D. farinae antigen. In babies who wheezed, a positive correlation was found between the total number of days that wheezing occurred and the blood eosinophil count. Babies who wheezed more often (> 20 days) had more peripheral blood basophils and eosinophils, and peripheral blood lymphocytes obtained from these subjects at the time of bronchiolitis produced less interferon gamma on stimulation with IL-2.
Bronchiolitis is followed by activation of cellular immunity, and early wheezing in infants is associated with a TH-2 response.
确定细胞免疫异常是否存在并与毛细支气管炎后的早期喘息相关。
我们前瞻性地研究了26名因首次发作毛细支气管炎而住院且无任何既往免疫、心脏或呼吸系统疾病的婴儿。在入组时和5个月后采集血液,以评估细胞总数和分类计数、CD4 +(辅助性)和CD8 +(抑制性/细胞毒性)淋巴细胞,以及活化标志物CD23(低亲和力免疫球蛋白E受体)和CD25(白细胞介素-2(IL-2)受体)。在用IL-2或屋尘螨(粉尘螨)抗原刺激后,在血浆和体外测量细胞因子干扰素γ(T辅助(TH)1型细胞因子)和IL-4(TH-2)。出院后家长记录每日喘息发作情况。
我们发现,与毛细支气管炎发作时以及同龄健康受试者相比,5个月时受试者的血液嗜酸性粒细胞增多,CD4 +、CD25 +和CD23 +淋巴细胞百分比增加(p < 0.05)。血浆IL-4水平虽然与健康受试者无差异,但也显著升高。毛细支气管炎后5个月,喘息婴儿的外周血淋巴细胞在体外对粉尘螨抗原产生更多的IL-4。在喘息婴儿中,喘息发生的总天数与血液嗜酸性粒细胞计数之间存在正相关。喘息更频繁(> 20天)的婴儿外周血嗜碱性粒细胞和嗜酸性粒细胞更多,在毛细支气管炎发作时从这些受试者获得外周血淋巴细胞在用IL-2刺激后产生的干扰素γ较少。
毛细支气管炎后细胞免疫激活,婴儿早期喘息与TH-2反应相关。