Shackelford P G, Granoff D M, Polmar S H, Scott M G, Goskowicz M C, Madassery J V, Nahm M H
Edward Mallinckrodt Department of Pediatrics, Washington University School of Medicine, St. Louis, MO 63110.
J Pediatr. 1990 Apr;116(4):529-38. doi: 10.1016/s0022-3476(05)81598-7.
To characterize more fully the immunologic basis for increased susceptibility to infection in patients with low serum concentrations of IgG2, we identified eight infection-prone children, 1 to 2 years of age, with serum IgG2 concentrations greater than 2 SD below the mean for age and followed their serologic and clinical courses for 1 to 3 years. Two of the eight children became clinically and immunologically normal and may have had transient IgG2 deficiency with an exaggerated developmental delay of this late-maturing subclass. The remaining six subjects had persistently subnormal or low-normal serum IgG2 levels and continued to experience frequent infections. All six of these children responded poorly to Haemophilus influenzae type b (Hib) polysaccharide, and four of six responded poorly to Streptococcus pneumoniae type 3 polysaccharide. Both IgG1 and IgG2-specific antibody responses to these vaccines were abnormal. Three of these six children also responded poorly to tetanus toxoid, an antigen that normally induces a predominant IgG1 response. Although five of these six children produced antibodies in response to Hib polysaccharide protein conjugate vaccine, three of four given Hib oligosaccharide CRM conjugate vaccine required booster doses to respond, a pattern of response characteristic of infants less than 6 months of age. Further, although serum concentrations of IgG1 were normal, peripheral blood mononuclear cells from four of six children tested produced extremely small amounts of IgG1 and IgG3 as well as IgG2. Finally, varied patterns of abnormalities of IgG, IgA, IgM, and IgG4 became apparent in five of the six children with persistently low serum IgG2 values. This study demonstrates that subnormal serum concentrations of IgG2 may be associated with varied patterns of immunologic dysfunction, some of which are evolving and may be responsible for increased susceptibility of these children to infection.
为了更全面地描述血清IgG2浓度低的患者易感染的免疫学基础,我们确定了8名1至2岁易感染的儿童,其血清IgG2浓度比年龄均值低2个标准差以上,并对他们的血清学和临床病程进行了1至3年的跟踪。8名儿童中有2名在临床和免疫学上恢复正常,可能患有短暂性IgG2缺乏症,且这种成熟较晚的亚类发育延迟过度。其余6名受试者的血清IgG2水平持续低于正常或略低于正常,并继续频繁感染。这6名儿童对b型流感嗜血杆菌(Hib)多糖的反应均较差,6名中有4名对3型肺炎链球菌多糖的反应也较差。对这些疫苗的IgG1和IgG2特异性抗体反应均异常。这6名儿童中有3名对破伤风类毒素的反应也较差,破伤风类毒素是一种通常诱导主要IgG1反应的抗原。尽管这6名儿童中有5名对Hib多糖蛋白结合疫苗产生了抗体,但在接种Hib寡糖CRM结合疫苗的4名儿童中,有3名需要加强剂量才能产生反应,这种反应模式是6个月以下婴儿的特征。此外,尽管IgG1的血清浓度正常,但在检测的6名儿童中有4名的外周血单个核细胞产生的IgG1、IgG3以及IgG2量极少。最后,在血清IgG2值持续偏低的6名儿童中,有5名出现了IgG、IgA、IgM和IgG4的各种异常模式。这项研究表明,血清IgG2浓度低于正常可能与多种免疫功能障碍模式相关,其中一些正在演变,可能是这些儿童易感染的原因。