Vella P P, Marburg S, Staub J M, Kniskern P J, Miller W, Hagopian A, Ip C, Tolman R L, Rusk C M, Chupak L S
Department of Cellular & Molecular Biology, Merck Sharp & Dohme Research Laboratories, West Point, Pennsylvania 19486.
Infect Immun. 1992 Dec;60(12):4977-83. doi: 10.1128/iai.60.12.4977-4983.1992.
In an effort to prepare pneumococcal (Pn) capsular polysaccharide (Ps) vaccines that would be immunogenic in infants, covalent conjugates were prepared for Pn types 6B, 14, 19F, and 23F. Each Ps type was covalently bound to an outer membrane protein complex from Neisseria meningitidis serogroup B and evaluated for immunogenicity in mice and infant monkeys. The conjugates induced specific anti-Ps antibody responses in mice and in infant rhesus and African green monkeys; a conjugate of 6B and outer membrane protein complex was immunogenic at Ps doses as low as 20 ng. Although low levels of the Pn group-common cell wall polysaccharide were present in all type-specific Ps preparations, anti-cell wall polysaccharide responses induced by covalent conjugates were < 1% of the total anti-Ps response after two doses of vaccine. In contrast, the anti-cell wall polysaccharide response of a noncovalent conjugate represented 41% of the anti-Ps response after two doses. Relative T-cell dependence, a requirement for the human target population of infants less than 18 months old, was demonstrated for all four Pn Ps conjugates in an athymic mouse model. Therefore, these Pn Ps-outer membrane protein complex conjugate vaccines are excellent candidates for evaluation in human infants.
为制备对婴儿具有免疫原性的肺炎球菌(Pn)荚膜多糖(Ps)疫苗,制备了6B、14、19F和23F型Pn的共价结合物。每种Ps类型都与B群脑膜炎奈瑟菌的外膜蛋白复合物共价结合,并在小鼠和幼猴中评估其免疫原性。这些结合物在小鼠、恒河猴幼猴和非洲绿猴中诱导了特异性抗Ps抗体反应;6B与外膜蛋白复合物的结合物在低至20 ng的Ps剂量下具有免疫原性。尽管在所有型特异性Ps制剂中都存在低水平的Pn组共同细胞壁多糖,但两剂疫苗后,共价结合物诱导的抗细胞壁多糖反应占总抗Ps反应的比例不到1%。相比之下,非共价结合物的抗细胞壁多糖反应在两剂后占抗Ps反应的41%。在无胸腺小鼠模型中,对所有四种Pn Ps结合物都证明了相对T细胞依赖性,这是18个月以下婴儿这一人类目标群体所需要的。因此,这些Pn Ps-外膜蛋白复合物结合疫苗是在人类婴儿中进行评估的优秀候选疫苗。