Oikawa Y, Ikeda T, Horii Y, Fujita K, Tsukidate S
Department of Medical Zoology, Kanazawa Medical University, Ishikawa, Japan.
Exp Parasitol. 1992 Aug;75(1):146-54. doi: 10.1016/0014-4894(92)90130-3.
Monoclonal antibodies against infective third-stage larvae (L3) of Brugia pahangi were generated from mice immunized with L3 antigens. The monoclonal antibodies were L3 stage-specific or stage-nonspecific. A BpG1 monoclonal antibody (IgG1 subclass) showing L3 stage-specificity was examined in detail. BpG1 recognized the surface of B. pahangi L3 and also reacted with the surface of Brugia malayi L3 but not with the surface of filarial worms of other genera, such as Acanthocheilonema viteae and Litomosoides carinii. BpG1 promoted cellular adhesion to the surface of B. pahangi L3. BpG1 bound on living L3 was shed but the shedding rate was relatively slow. The surface antigen recognized by BpG1 had a molecular weight of 58 kDa. It was stable to heat and periodate treatments but sensitive to trypsin digestion and was released from living L3 by SDS but not by Triton X-100 or CTAB. Preincubation of L3 with BpG1 significantly reduced the recovery rate of worms compared with the preincubation with a monoclonal antibody (IgG1 subclass) against the inner tissues of B. pahangi L3 or control supernatant of P3U1 myeloma cells. This result suggests that the antigen containing the BpG1 epitope may be one of the targets of a protective immune response against Brugia infection.
用彭亨丝虫感染性三期幼虫(L3)抗原免疫小鼠,产生了针对该幼虫的单克隆抗体。这些单克隆抗体具有L3阶段特异性或非阶段特异性。对一种显示L3阶段特异性的BpG1单克隆抗体(IgG1亚类)进行了详细研究。BpG1识别彭亨丝虫L3的表面,也与马来丝虫L3的表面发生反应,但不与其他属的丝虫表面反应,如旋盘尾丝虫和卡里尼丝虫。BpG1促进细胞黏附于彭亨丝虫L3的表面。结合在活L3上的BpG1会脱落,但脱落速率相对较慢。BpG1识别的表面抗原分子量为58 kDa。它对加热和高碘酸盐处理稳定,但对胰蛋白酶消化敏感,可通过SDS从活L3中释放出来,但不能通过Triton X-100或CTAB释放。与用针对彭亨丝虫L3内部组织的单克隆抗体(IgG1亚类)或P3U1骨髓瘤细胞的对照上清液预孵育相比,用BpG1预孵育L3显著降低了虫体回收率。这一结果表明,含有BpG1表位的抗原可能是针对丝虫感染的保护性免疫反应的靶点之一。