Karampatsas Konstantinos, Hall Tom, Voysey Merryn, Carreras-Abad Clara, Cochet Madeleine, Ramkhelawon Laxmee, Peregrine Elisabeth, Andrews Nick, Heath Paul T, Le Doare Kirsty
Centre for Neonatal and Paediatric Infection, St. George's, University of London, London, United Kingdom.
Centre for Neonatal and Paediatric Infection, St. George's, University of London, London, United Kingdom.
Vaccine. 2024 May 10;42(13):3230-3238. doi: 10.1016/j.vaccine.2024.04.014. Epub 2024 Apr 15.
Capsular polysaccharide (CPS) serotype-specific Immunoglobulin G (IgG) in cord blood has been proposed as a correlate of protection against invasive Group B Streptococcus (iGBS) disease. Although protective levels are required in infants throughout the window of vulnerability up to 3 months of age, little is known regarding the kinetics of GBS-specific IgG over this period.
We enrolled 33 healthy infants born to mothers colonized with GBS. We collected cord blood and infant blood samples either at one (21-35 days), two (49-63 days), or three months of age (77-91 days). We measured GBS serotype-specific CPS IgG concentrations and calculated the decay rate using a mixed-effects model. We further explored whether the antibody kinetics were affected by common maternal and infant factors and estimated the correlation between IgG concentration at birth and one, two, and three months of age.
The half-life estimate of IgG concentration for homologous and non-homologous GBS serotypes in paired samples with detectable IgG levels at both time points was 27.4 (95 % CI: 23.5-32.9) days. The decay rate did not vary by maternal age (p = 0.7), ethnicity (p = 0.1), gravida (p = 0.1), gestation (p = 0.7), and infant sex (p = 0.1). Predicted IgG titres above the assay lower limit of quantification on day 30 strongly correlated with titres at birth (Spearman correlation coefficient 0.71 [95 % CI: 0.60-0.80]).
Our results provide a basis for future investigations into the use of antibody kinetics in defining a serocorrelate of protection against late-onset iGBS disease.
脐带血中荚膜多糖(CPS)血清型特异性免疫球蛋白G(IgG)被认为是预防侵袭性B族链球菌(iGBS)疾病的一个相关指标。尽管在长达3个月的易感染窗口期内,婴儿都需要有保护性水平的抗体,但在此期间GBS特异性IgG的动力学情况却鲜为人知。
我们招募了33名母亲为GBS定植菌携带者的健康婴儿。在婴儿1个月(21 - 35天)、2个月(49 - 63天)或3个月(77 - 91天)时采集脐带血和婴儿血样本。我们测量了GBS血清型特异性CPS IgG浓度,并使用混合效应模型计算衰减率。我们进一步探讨了抗体动力学是否受常见母婴因素的影响,并估计了出生时及1个月、2个月和3个月时IgG浓度之间的相关性。
在两个时间点均检测到可检测IgG水平的配对样本中(针对同源和非同源GBS血清型),IgG浓度的半衰期估计值为27.4(95%可信区间:23.5 - 32.9)天。衰减率不受母亲年龄(p = 0.7)、种族(p = 0.1)、孕次(p = 0.1)、孕周(p = 0.7)和婴儿性别(p = 0.1)的影响。出生后30天高于检测定量下限的预测IgG滴度与出生时的滴度密切相关(斯皮尔曼相关系数0.71 [95%可信区间:0.60 - 0.80])。
我们的结果为未来研究利用抗体动力学来定义预防迟发性iGBS疾病的血清学相关指标提供了依据。