Wysocki Jacek, Brzostek Jerzy, Konior Ryszard, Panzer Falko G, François Nancy A, Ravula Sudheer M, Kolhe Devayani A, Song Yue, Dieussaert Ilse, Schuerman Lode, Borys Dorota
a Department of Preventive Medicine , Poznan University School of Medical Sciences , Poznan , Poland.
b Pediatrics Department , Zespol Opieki Zdrowotnej w Debicy , Debica , Poland.
Hum Vaccin Immunother. 2017 Mar 4;13(3):661-675. doi: 10.1080/21645515.2016.1241919. Epub 2016 Oct 13.
To investigate long-term antibody persistence following the administration of the 10-valent pneumococcal non-typeable Haemophilus influenzae protein D conjugate vaccine (PHiD-CV), we present results of 2 follow-up studies assessing antibody persistence following 2 3+1 schedules up to 4 (NCT00624819 - Study A) and 5 years (NCT00891176 - Study B) post-booster vaccination. In Study A, antibody persistence was measured one, 2 and 4 years post-booster in children previously primed and boosted with PHiD-CV, or primed with the 7-valent pneumococcal conjugate vaccine (7vCRM) and boosted with either PHiD-CV or 7vCRM. In Study B, PHiD-CV was co-administered with meningococcal vaccines, and pneumococcal antibody persistence was measured 2, 3 and 5 years post-booster. An age-matched control group, unvaccinated against Streptococcus pneumoniae, was enrolled in Study A, allowing assessment of immunologic memory by administration of one dose of PHiD-CV to both primed (4 years post-booster) and unprimed 6-year-old children. Four years post-booster (Study A), antibody concentrations and opsonophagocytic activity (OPA) titers remained higher compared to the pre-booster timepoint, with no major differences between the 3 primed groups. Antibody persistence was also observed in Study B, with minimal differences between groups. The additional PHiD-CV dose administered 4 years post-booster in Study A elicited more robust immune responses in primed children than in unprimed children. Long-term serotype-specific antibody persistence and robust immunologic memory responses observed in these 2 studies suggest induction of long-term protection against pneumococcal disease after PHiD-CV vaccination.
为了研究10价肺炎球菌非分型流感嗜血杆菌蛋白D结合疫苗(PHiD-CV)接种后的长期抗体持久性,我们展示了两项随访研究的结果,这两项研究评估了在加强免疫后长达4年(NCT00624819 - 研究A)和5年(NCT00891176 - 研究B)的两种3+1接种程序后的抗体持久性。在研究A中,对先前用PHiD-CV进行过基础免疫和加强免疫的儿童,或用7价肺炎球菌结合疫苗(7vCRM)进行过基础免疫并随后用PHiD-CV或7vCRM进行加强免疫的儿童,在加强免疫后1年、2年和4年测量抗体持久性。在研究B中,PHiD-CV与脑膜炎球菌疫苗联合接种,并在加强免疫后2年、3年和5年测量肺炎球菌抗体持久性。研究A纳入了一个未接种肺炎链球菌疫苗的年龄匹配对照组,通过对已进行基础免疫(加强免疫后4年)和未进行基础免疫的6岁儿童接种一剂PHiD-CV来评估免疫记忆。加强免疫后4年(研究A),与加强免疫前的时间点相比,抗体浓度和调理吞噬活性(OPA)滴度仍然更高,3个已进行基础免疫的组之间没有重大差异。在研究B中也观察到了抗体持久性,各群组之间差异极小。研究A中在加强免疫后4年给予的额外一剂PHiD-CV在已进行基础免疫的儿童中引发的免疫反应比未进行基础免疫的儿童更强。在这两项研究中观察到的长期血清型特异性抗体持久性和强大的免疫记忆反应表明,接种PHiD-CV后可诱导对肺炎球菌疾病的长期保护。