Obaro Stephen K, Deubzer Hedwig E, Newman Vanessa O, Adegbola Richard A, Greenwood Brian M, Henderson Don C
Imperial College, School of Science, Technology and Medicine, Department of Immunology, Chelsea and Westminster Hospital, London, United Kingdom.
Pediatr Infect Dis J. 2004 Nov;23(11):1023-9. doi: 10.1097/01.inf.0000143651.54880.09.
In breast-feeding populations, immunization during pregnancy with pneumococcal polysaccharide offers a potentially useful approach to preventing pneumococcal disease in young infants.
Breast milk samples were collected at 0, 2, 4 and 6 months after delivery from Gambian women vaccinated during pregnancy (24-32 weeks gestation) with Pneumovax II (n = 56) or Mengivax A&C (n = 57). Specimens were examined for secretory immunoglobulin A (s-IgA) concentration, subclass distribution and avidity specific to pneumococcal serotypes 4, 6B, 14, 19F and 23F and the antigen mixture in Pneumovax II by enzyme-linked immunosorbent assay. Colostral s-IgA and IgG concentrations in paired maternal sera were compared.
Colostral s-IgA concentrations specific to all pneumococcal polysaccharide antigens investigated were significantly higher (P < 0.05) among Pneumovax II vaccinees. Titers specific to serotypes 4, 6B and 14 and the vaccine formula remained significantly higher during 6 months, and those for 19F were higher during 4 months. Significantly higher concentrations of vaccine antigen-specific s-IgA antibody were sustained for 6 months after delivery (P = 0.011). Comparison of colostral s-IgA and IgG in serum revealed a significant correlation only among Mengivax A&C vaccinees for pneumococcal polysaccharide 23F (rs= 0.68; P < or = 0.0001). Vaccination elicited trends toward increased s-IgA2, reaching significance for serotype 14 and the vaccine formula. Immunization elicited significantly higher s-IgA avidities specific to all pneumococcal polysaccharide antigens studied during 6 months.
The public health value of immunization during pregnancy with pneumococcal polysaccharide vaccine in breast-feeding populations warrants further evaluation, particularly in populations with a high incidence of pneumococcal disease in early infancy.
在母乳喂养人群中,孕期接种肺炎球菌多糖疫苗为预防幼儿肺炎球菌疾病提供了一种潜在的有效方法。
从孕期(妊娠24 - 32周)接种了Pneumovax II(n = 56)或Mengivax A&C(n = 57)的冈比亚妇女产后0、2、4和6个月收集母乳样本。通过酶联免疫吸附测定法检测样本中分泌型免疫球蛋白A(s-IgA)浓度、亚类分布以及针对肺炎球菌4、6B、14、19F和23F血清型及Pneumovax II中抗原混合物的亲和力。比较配对母血清中初乳s-IgA和IgG浓度。
在接种Pneumovax II的人群中,所有研究的肺炎球菌多糖抗原特异性初乳s-IgA浓度显著更高(P < 0.05)。针对4、6B和14血清型以及疫苗配方的滴度在6个月内仍显著更高,针对19F的滴度在4个月内更高。产后6个月内,疫苗抗原特异性s-IgA抗体浓度持续显著更高(P = 0.011)。血清中初乳s-IgA和IgG的比较显示,仅在接种Mengivax A&C的人群中,肺炎球菌多糖23F存在显著相关性(rs = 0.68;P ≤ 0.0001)。接种疫苗引发s-IgA2增加趋势,14血清型和疫苗配方达到显著水平。免疫接种在6个月内引发所有研究的肺炎球菌多糖抗原特异性s-IgA亲和力显著更高。
孕期接种肺炎球菌多糖疫苗在母乳喂养人群中的公共卫生价值值得进一步评估,特别是在婴儿早期肺炎球菌疾病发病率高的人群中。