Gu X X, Tsai C M
Center for Biologics Evaluation and Research, Food and Drug Administration, Bethesda, Maryland 20892.
Infect Immun. 1993 May;61(5):1873-80. doi: 10.1128/iai.61.5.1873-1880.1993.
A method was developed for coupling carboxylic acid-containing oligosaccharides (OS) to proteins. An OS was isolated from Neisseria meningitidis group A strain A1 lipooligosaccharide (LOS). This LOS has no human glycolipid-like lacto-N-neotetraose structure and contains multiple immunotypes, including L8, found in group B and C strains. The carboxylic acid at 2-keto-3-deoxyoctulosonic acid of the OS was linked through adipic acid dihydrazide to tetanus toxoid. The molar ratio of the OS to tetanus toxoid in three conjugates ranged from 11:1 to 19:1. The antigenicity of the OS was conserved in these conjugates, as measured by an enzyme-linked immunosorbent assay (ELISA) and an inhibition ELISA with polyclonal and monoclonal antibodies to A1 LOS. These conjugates induced immunoglobulin G antibodies to A1 LOS in mice and rabbits. The immunogenicity of the conjugates in rabbits was enhanced by use of monophosphoryl lipid A plus trehalose dimycolate as an adjuvant. The resulting rabbit antisera cross-reacted with most of 12 prototype LOSs and with LOSs from two group B disease strains, 44/76 and BB431, in an ELISA and in Western blotting (immunoblotting), which revealed a 3.6-kDa reactive band in these LOSs. The rabbit antisera showed bactericidal activity against homologous strain A1 and heterologous strains 44/76 and BB431. These results indicate that conjugates derived from A1 LOS can induce antibodies against many LOS immunotypes from different organism serogroups, including group B. OS-protein conjugates derived from meningococcal LOSs may therefore be candidate vaccines to prevent meningitis caused by meningococci.
开发了一种将含羧酸的寡糖(OS)与蛋白质偶联的方法。从A群脑膜炎奈瑟菌A1株脂寡糖(LOS)中分离出一种OS。该LOS不具有人糖脂样乳糖-N-新四糖结构,且包含多种免疫型,包括在B群和C群菌株中发现的L8。OS的2-酮-3-脱氧辛糖酸上的羧酸通过己二酸二酰肼与破伤风类毒素相连。三种偶联物中OS与破伤风类毒素的摩尔比为11:1至19:1。通过酶联免疫吸附测定(ELISA)以及使用针对A1 LOS的多克隆和单克隆抗体的抑制ELISA测量发现,这些偶联物中OS的抗原性得以保留。这些偶联物在小鼠和兔子体内诱导产生了针对A1 LOS的免疫球蛋白G抗体。通过使用单磷酰脂质A加海藻糖二霉菌酸酯作为佐剂,增强了偶联物在兔子体内的免疫原性。在ELISA和蛋白质印迹法(免疫印迹)中,所得兔抗血清与12种原型LOS中的大多数以及来自两种B群疾病菌株44/76和BB431的LOS发生交叉反应,蛋白质印迹法显示这些LOS中有一条3.6 kDa的反应带。兔抗血清对同源菌株A1以及异源菌株44/76和BB431具有杀菌活性。这些结果表明,源自A1 LOS的偶联物可诱导产生针对来自不同生物体血清群(包括B群)的许多LOS免疫型的抗体。因此,源自脑膜炎球菌LOS的OS-蛋白质偶联物可能是预防脑膜炎球菌引起的脑膜炎的候选疫苗。