Diallo Aldiouma, Sow Samba O, Idoko Olubukola T, Hirve Siddhivinayak, Findlow Helen, Preziosi Marie-Pierre, Elie Cheryl, Kulkarni Prasad S, Parulekar Varsha, Diarra Bou, Cheick Haidara Fadima, Diallo Fatoumata, Tapia Milagritos, Akinsola Adebayo K, Adegbola Richard A, Bavdekar Ashish, Juvekar Sanjay, Chaumont Julie, Martellet Lionel, Marchetti Elisa, LaForce Marc F, Plikaytis Brian D, Enwere Godwin C, Tang Yuxiao, Borrow Ray, Carlone George, Viviani Simonetta
Institut de Recherche pour le Développement, Niakhar, Sénégal.
Centre pour le Développement des Vaccins, Ministère de la Santé, Bamako, Mali.
Clin Infect Dis. 2015 Nov 15;61 Suppl 5(Suppl 5):S521-30. doi: 10.1093/cid/civ518.
Mass vaccination campaigns of the population aged 1-29 years with 1 dose of group A meningococcal (MenA) conjugate vaccine (PsA-TT, MenAfriVac) in African meningitis belt countries has resulted in the near-disappearance of MenA. The vaccine was tested in clinical trials in Africa and in India and found to be safe and highly immunogenic compared with the group A component of the licensed quadrivalent polysaccharide vaccine (PsACWY). Antibody persistence in Africa and in India was investigated.
A total of 900 subjects aged 2-29 years were followed up for 4 years in Senegal, Mali, and The Gambia (study A). A total of 340 subjects aged 2-10 years were followed up for 1 year in India (study B). In study A, subjects were randomized in a 2:1 ratio, and in study B a 1:1 ratio to receive either PsA-TT or PsACWY. Immunogenicity was evaluated by measuring MenA serum bactericidal antibody (SBA) with rabbit complement and by a group A-specific immunoglobulin G (IgG) enzyme-linked immunosorbent assay.
In both studies, substantial SBA decay was observed at 6 months postvaccination in both vaccine groups, although more marked in the PsACWY group. At 1 year and 4 years (only for study A) postvaccination, SBA titers were relatively sustained in the PsA-TT group, whereas a slight increasing trend, more pronounced among the youngest, was observed in the participants aged <18 years in the PsACWY groups. The SBA titers were significantly higher in the PsA-TT group than in the PsACWY group at any time point, and the majority of subjects in the PsA-TT group had SBA titers ≥128 and group A-specific IgG concentrations ≥2 µg/mL at any point in time in both the African and Indian study populations.
Four years after vaccination with a single dose of PsA-TT vaccine in Africa, most subjects are considered protected from MenA disease.
PsA-TT-003 (ISRCTN87739946); PsA-TT-003a (ISRCTN46335400).
在非洲脑膜炎带国家,对1至29岁人群开展单剂A群脑膜炎球菌(MenA)结合疫苗(PsA-TT,MenAfriVac)大规模疫苗接种运动后,A群脑膜炎球菌几乎消失。该疫苗在非洲和印度进行了临床试验,与已获许可的四价多糖疫苗(PsACWY)的A群成分相比,被发现安全且具有高度免疫原性。对非洲和印度的抗体持久性进行了研究。
在塞内加尔、马里和冈比亚,对900名2至29岁的受试者进行了4年的随访(研究A)。在印度,对340名2至10岁的受试者进行了1年的随访(研究B)。在研究A中,受试者按2:1的比例随机分组,在研究B中按1:1的比例随机分组,以接受PsA-TT或PsACWY。通过用兔补体测量MenA血清杀菌抗体(SBA)以及通过A群特异性免疫球蛋白G(IgG)酶联免疫吸附测定来评估免疫原性。
在两项研究中,两个疫苗组在接种疫苗后6个月均观察到SBA显著下降,尽管在PsACWY组中更为明显。在接种疫苗后1年和4年(仅针对研究A),PsA-TT组的SBA滴度相对稳定,而在PsACWY组中,<18岁的参与者中观察到轻微的上升趋势,在最年轻的参与者中更为明显。在任何时间点,PsA-TT组的SBA滴度均显著高于PsACWY组,并且在非洲和印度的研究人群中,PsA-TT组的大多数受试者在任何时间点的SBA滴度均≥128,且A群特异性IgG浓度≥2μg/mL。
在非洲接种单剂PsA-TT疫苗四年后,大多数受试者被认为对A群脑膜炎球菌病具有免疫力。
PsA-TT-003(ISRCTN87739946);PsA-TT-003a(ISRCTN46335400)。