National Institute for Communicable Diseases - Division of National Health Laboratory Service, Centre for Vaccines and Immunology, Sandringham, South Africa.
Vaccine. 2013 Jan 21;31(5):777-83. doi: 10.1016/j.vaccine.2012.11.076. Epub 2012 Dec 8.
The immunogenicity of pneumococcal conjugate vaccine (PCV) has not been evaluated in HIV-infected infants following the first and second PCV-doses. We studied antibody kinetics of serotypes included in 7-valent PCV in HIV-infected and HIV-uninfected infants prior to and following each of three PCV-doses.
HIV-uninfected infants born to HIV-uninfected (HUU) and HIV-infected mothers (HEU); and perinatal HIV-infected children with CD(4+)<25% randomized to initiate antiretroviral treatment (ART) when clinically and/or immunologically indicated (ART-) or immediately (ART+) were enrolled. Vaccination occurred at approximately 7.4, 11.5 and 15.5 weeks of age. Serotype-specific antibody was measured by ELISA following each PCV-dose and opsonophagocytic activity (OPA) to three serotypes following the second and third doses.
Pre-vaccination, antibody geometric mean concentrations (GMCs) were higher in HUU compared to HIV-exposed groups for most serotypes. GMCs and proportion of infants with antibody ≥0.35 μg/ml were similar in HUU compared to other groups following the second PCV-dose. In all groups, GMCs were greater following the third compared to post-second dose; and a higher proportion within each group had antibody ≥0.35 μg/ml to 6B and 23F. OPA GMTs increased after the third compared to post-second dose for studied-serotypes; as did the proportion with OPA ≥8 to 23F.
A two-dose primary-series of PCV probably confers similar protection against invasive pneumococcal disease in HIV-infected compared to HUU children. The inferior response to serotypes 6B and 23F, and lower GMCs and OPA GMTs, following two compared to after three PCV-doses may have implications in the prevention of pneumococcal disease in high-burden countries.
尚未评估 HIV 感染婴儿在接种第一和第二剂肺炎球菌结合疫苗(PCV)后,PCV 的免疫原性。我们研究了在接受每 3 剂 PCV 之前和之后,7 价 PCV 中包含的血清型在 HIV 感染和未感染婴儿中的抗体动力学。
HIV 未感染婴儿(HUU)和 HIV 感染母亲(HEU)出生的婴儿;以及 CD(4+)<25%的围产期 HIV 感染儿童,在临床和/或免疫上需要时(ART-)或立即(ART+)开始抗逆转录病毒治疗(ART),随机分组。疫苗接种于约 7.4、11.5 和 15.5 周龄进行。在接受每剂 PCV 后,通过 ELISA 测量血清型特异性抗体,在接受第二和第三剂后,测量三种血清型的调理吞噬活性(OPA)。
在接种前,对于大多数血清型,HUU 的抗体几何平均浓度(GMC)高于 HIV 暴露组。在接受第二剂 PCV 后,与 HIV 暴露组相比,HUU 的 GMC 和具有抗体≥0.35μg/ml 的婴儿比例相似。在所有组中,第三剂后的 GMC 均高于第二剂后;并且每组中具有抗体≥0.35μg/ml 的比例更高。在研究的血清型中,第三剂后的 OPA GMT 高于第二剂后;并且具有 OPA≥8 的比例也增加。
两剂初级 PCV 系列可能在预防 HIV 感染儿童与 HUU 儿童的侵袭性肺炎球菌病方面提供相似的保护。与接种三剂 PCV 后相比,接种两剂后 6B 和 23F 血清型的反应较差,GMC 和 OPA GMT 较低,这可能对高负担国家预防肺炎球菌病产生影响。