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针对脑膜炎奈瑟菌PorA的鼠单克隆抗体在幼鼠感染模型中对B:15:P1.7,16亚型变体的体内保护活性降低。

Murine monoclonal antibodies to PorA of Neisseria meningitidis show reduced protective activity in vivo against B:15:P1.7,16 subtype variants in an infant rat infection model.

作者信息

Toropainen M, Saarinen L, van der Ley P, Kuipers B, Käyhty H

机构信息

National Public Health Institute, Helsinki, Finland.

出版信息

Microb Pathog. 2001 Mar;30(3):139-48. doi: 10.1006/mpat.2000.0419.

Abstract

The major outer membrane protein PorA of Neisseria meningitidis is the target for bactericidal serosubtyping antibodies and is currently considered as a potential vaccine candidate against group B meningococcal disease. Although the minor antigenic variability of the PorA has been increasingly recognized and described, its implication for vaccine design remains unclear. In this study, the protective activity of murine monoclonal PorA specific antibodies against four isogenic meningococcal P1.7,16 target strains, the prototype P1.7,16a and three loop 4 point mutation variants (designated P1.7,16b to d) constructed from reference strain H44/76 (B:15:P1.7,16a), was evaluated in the infant rat infection model. All monoclonal antibodies had been obtained by immunization of mice with outer membrane protein preparations from meningococcal serosubtype P1.7,16 reference strain H44/76. A challenge dose of 10(5)cfu/pup was given i.p. 1-2 h after the i.p. injection of 1:100 diluted antibodies, and the development of bacteremia was assessed by culturing blood samples taken 6 h after challenge. MN14C11.6, a reference monoclonal antibody for serosubtype P1.7 epitope located in predicted loop 1 (VR1) identical in all the variants, was equally protective against all loop 4 variants. The three P1.16 specific monoclonal antibodies tested (MN5C11G, MN12H2 and 62D12-8) all completely protected animals against the prototype P1.7,16a, variably against the P1.7,16b and P1.7,16c, but not against the P1.7,16d variant. Our findings therefore suggest that certain subtype variants may escape protection in vivo conferred by PorA specific antibodies.

摘要

脑膜炎奈瑟菌的主要外膜蛋白PorA是杀菌血清亚型分型抗体的靶点,目前被认为是预防B群脑膜炎球菌病的潜在疫苗候选物。尽管PorA的微小抗原变异性已得到越来越多的认识和描述,但其对疫苗设计的影响仍不清楚。在本研究中,在幼鼠感染模型中评估了鼠源单克隆PorA特异性抗体对四种同基因脑膜炎球菌P1.7,16靶菌株(原型P1.7,16a以及由参考菌株H44/76(B:15:P1.7,16a)构建的三个环4点突变变体(命名为P1.7,16b至d))的保护活性。所有单克隆抗体均通过用脑膜炎球菌血清亚型P1.7,16参考菌株H44/76的外膜蛋白制剂免疫小鼠获得。在腹腔注射1:100稀释抗体后1-2小时,腹腔给予10(5)cfu/只的攻击剂量,通过培养攻击后6小时采集的血样评估菌血症的发生情况。MN14C11.6是一种针对位于预测环1(VR1)中且在所有变体中均相同的P1.7血清型表位的参考单克隆抗体,对所有环4变体具有同等的保护作用。所测试的三种P1.16特异性单克隆抗体(MN5C11G、MN12H2和62D12-8)均能完全保护动物免受原型P1.7,16a的侵害,对P1.7,16b和P1.7,16c有不同程度的保护作用,但对P1.7,16d变体无保护作用。因此,我们的研究结果表明,某些亚型变体可能逃避PorA特异性抗体在体内赋予的保护作用。

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