Dicko Alassane, Dicko Yahia, Barry Amadou, Sidibe Youssoufa, Mahamar Almahamoudou, Santara Gaoussou, Dolo Amagana, Diallo Aminata, Doumbo Ogobara, Shafi Fakrudeen, François Nancy, Yarzabal Juan Pablo, Strezova Ana, Borys Dorota, Schuerman Lode
a Malaria Research and Training Center; Faculty of Medicine; Pharmacy and Dentistry; University of Bamako ; Bamako , Mali.
Hum Vaccin Immunother. 2015;11(9):2207-14. doi: 10.1080/21645515.2015.1016679.
Pneumonia is still the leading cause of death among African children with pneumococcal serotypes 1 and 5 being dominant in the below 5 y of age group. The present study assessed the safety, reactogenicity and immunogenicity of a 2-dose catch-up vaccination with the 10-valent pneumococcal non-typeable Haemophilus influenzae Protein D conjugate vaccine (PHiD-CV) in Malian children. This phase III, open-label study (NCT00985465) was conducted in Ouelessebougou, Mali, between November 2009 and July 2010. The study population consisted of PHiD-CV unprimed Malian children previously enrolled in the control group of study NCT00678301 receiving a 2-dose catch-up vaccination with PHiD-CV in the second year of life. Adverse events were recorded following each PHiD-CV dose. Antibody responses and opsonophagocytic activity (OPA) were measured pre-vaccination and after the second PHiD-CV catch-up dose. Swelling and fever (axillary temperature ≥ 37.5°C) were the most frequently reported solicited symptoms following either PHiD-CV dose. Few grade 3 solicited symptoms were reported. Large swelling reactions and serious adverse events were not reported. Post-catch-up vaccination, for each vaccine pneumococcal serotype, at least 94.7% of subjects had antibody concentrations ≥ 0.2 μg/ml, except for serotypes 6B (82.5%) and 23F (87.7%). At least 94.0% of subjects had OPA titres ≥ 8, except for serotype 19F (89.4%). The geometric mean concentration for antibodies against protein D was 839.3 (95% CI: 643.5-1094.6) EL.U/ml. Two-dose PHiD-CV catch-up regimen in the second year of life was well-tolerated and immunogenic for all vaccine pneumococcal serotypes and NTHi protein D when administered to Malian children.
肺炎仍是非洲儿童死亡的主要原因,其中1型和5型肺炎球菌血清型在5岁以下年龄组中占主导地位。本研究评估了在马里儿童中使用10价肺炎球菌非分型流感嗜血杆菌蛋白D结合疫苗(PHiD-CV)进行2剂补种疫苗的安全性、反应原性和免疫原性。这项III期开放标签研究(NCT00985465)于2009年11月至2010年7月在马里的韦莱塞布古进行。研究人群包括之前参加NCT00678301研究对照组的未接种过PHiD-CV的马里儿童,这些儿童在生命的第二年接受了2剂PHiD-CV补种疫苗。每次接种PHiD-CV后记录不良事件。在接种前和第二次接种PHiD-CV补种疫苗后测量抗体反应和吞噬细胞杀菌活性(OPA)。肿胀和发热(腋下温度≥37.5°C)是接种任何一剂PHiD-CV后最常报告的预期症状。报告的3级预期症状很少。未报告大的肿胀反应和严重不良事件。补种疫苗后,对于每种疫苗肺炎球菌血清型,除6B型(82.5%)和23F型(87.7%)外,至少94.7%的受试者抗体浓度≥0.2μg/ml。除19F型(89.4%)外,至少94.0%的受试者OPA滴度≥8。抗蛋白D抗体的几何平均浓度为839.3(95%CI:643.5-1094.6)EL.U/ml。在马里儿童中,生命第二年的2剂PHiD-CV补种方案对所有疫苗肺炎球菌血清型和非典型流感嗜血杆菌蛋白D具有良好的耐受性和免疫原性。