Lachenauer Catherine S, Baker Carol J, Baron Miriam J, Kasper Dennis L, Gravekamp Claudia, Madoff Lawrence C
Channing Laboratory and Division of Infectious Diseases, Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.
J Infect Dis. 2002 Feb 1;185(3):368-74. doi: 10.1086/338773. Epub 2002 Jan 17.
The beta C protein of group B streptococci (GBS) elicits antibody that is protective against GBS challenge in animals and is considered to be a potential component of a GBS conjugate vaccine. We developed a quantitative enzyme-linked immunosorbent assay to measure beta-specific serum immunoglobulin G (IgG) levels and used it to compare beta-specific IgG in a group of mothers of neonates with invasive type Ib/beta GBS disease and a group of mothers colonized with Ib/beta strains whose neonates remained well. beta-Specific IgG concentrations from these 2 groups were similar. To investigate differences in beta-specific antibody in animals and humans, protein fragments were generated that corresponded to major regions within the beta C protein. A single major region was predominantly recognized in human and rabbit serum samples. Thus, in contrast to immunized animals, no relationship was seen between levels of naturally acquired human beta-specific IgG and protection from neonatal disease. This difference was not explained by a major difference in epitope specificity.
B族链球菌(GBS)的βC蛋白可诱导产生抗体,该抗体在动物实验中对GBS攻击具有保护作用,被认为是GBS结合疫苗的潜在成分。我们开发了一种定量酶联免疫吸附测定法来测量β特异性血清免疫球蛋白G(IgG)水平,并使用该方法比较了一组患有侵袭性Ib/β型GBS疾病的新生儿母亲和一组携带Ib/β菌株但其新生儿健康的母亲体内的β特异性IgG。这两组母亲的β特异性IgG浓度相似。为了研究动物和人类β特异性抗体的差异,我们制备了与βC蛋白主要区域相对应的蛋白质片段。在人类和兔血清样本中,一个主要区域被优先识别。因此,与免疫动物不同,天然获得的人类β特异性IgG水平与预防新生儿疾病之间没有关联。这种差异不能用表位特异性的重大差异来解释。