Department of Pediatric and Adolescent Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Postgrad Med. 2010 Sep;122(5):116-24. doi: 10.3810/pgm.2010.09.2208.
Asthma has been reported to be associated with an increased risk of invasive pneumococcal disease (IPD).
We compared serotype-specific antibody responses with pneumococcal polysaccharide antigens of individuals with and without asthma.
A cross-sectional study was conducted for 16 subjects with asthma and 14 subjects without asthma from the community of Rochester, MN. Asthma was determined by predetermined criteria based on comprehensive medical record reviews. Serotype-specific antibody to 23 pneumococcal polysaccharide antigens was measured by enzyme-linked immunosorbent assay, and seropositivity was considered ≥ 1.3 μg/mL. Interferon-γ (IFN-γ) and interleukin-5 (IL-5) were measured from peripheral blood mononuclear cells cultured with house dust mites and staphylococcal enterotoxin B.
Of the 30 subjects, 16 (53%) were male, 21 (70%) were white, and the median age was 26 years. The median numbers of positive serotype-specific antibodies for asthmatics and nonasthmatics were 8.5 and 15.5, respectively (P = 0.034). There was an inverse relationship between the ratio of log-transformed IL-5/IFN-γ and the number of positive serotype-specific antibodies (r = -0.36; P = 0.052). As potential covariates and confounders, a history of pneumococcal vaccination (P = 0.84), having a high-risk condition for IPD (P = 0.68), and taking asthma medications, including inhaled/systemic corticosteroids (P = 0.79), were not associated with the number of positive serotype-specific antibodies.
Asthmatics had significantly lower serotype-specific pneumococcal antibody levels than nonasthmatics. House dust mite-induced T-helper 2 (Th2) cytokine immune profile may be related to the association. This may account for an increased risk of IPD in asthmatics and deserves further investigation.
据报道,哮喘与侵袭性肺炎球菌病(IPD)的风险增加有关。
我们比较了有和没有哮喘的个体对肺炎球菌多糖抗原的血清型特异性抗体反应。
在明尼苏达州罗彻斯特的社区中,对 16 名哮喘患者和 14 名非哮喘患者进行了横断面研究。哮喘通过基于全面病历回顾的预定标准确定。通过酶联免疫吸附试验测量针对 23 种肺炎球菌多糖抗原的血清型特异性抗体,并且将血清阳性定义为≥1.3μg/mL。用屋尘螨和葡萄球菌肠毒素 B 培养外周血单个核细胞,测量干扰素-γ(IFN-γ)和白细胞介素-5(IL-5)。
在 30 名受试者中,16 名(53%)为男性,21 名(70%)为白人,中位年龄为 26 岁。哮喘患者和非哮喘患者的阳性血清型特异性抗体中位数分别为 8.5 和 15.5(P=0.034)。哮喘患者和非哮喘患者的对数转换后 IL-5/IFN-γ 比值与阳性血清型特异性抗体数量之间存在负相关(r=-0.36;P=0.052)。作为潜在的协变量和混杂因素,肺炎球菌疫苗接种史(P=0.84)、具有 IPD 高危因素(P=0.68)以及使用哮喘药物,包括吸入/全身皮质类固醇(P=0.79)与阳性血清型特异性抗体数量无关。
哮喘患者的血清型特异性肺炎球菌抗体水平明显低于非哮喘患者。屋尘螨诱导的辅助性 T 细胞(Th2)细胞因子免疫谱可能与这种关联有关。这可能解释了哮喘患者 IPD 风险增加的原因,值得进一步研究。