Burkot T R, Kwan-Lim G E, Maizels R M
Queensland Institute of Medical Research, Australia.
Infect Immun. 1996 Feb;64(2):485-8. doi: 10.1128/iai.64.2.485-488.1996.
CBA and BALB/c mice produced polyspecific and monospecific polyclonal antibody responses, respectively, following immunization with Wuchereria bancrofti stage-3 larvae. Two monoclonal antibodies (MAbs) were produced from the immunized BALB/c mouse. These MAbs (both isotype M) recognized a previously undescribed highly expressed W. bancrofti antigen present in stage-3 larvae. The epitopes bound by the MAbs appear to be species specific for W. bancrofti since the MAbs did not bind to antigens of either nine other nematode species or two vector species in Western blots (immunoblots). Phosphorylcholine epitopes, responsible for immunological cross-reactivity among nematodes, were identified only on a 200-kDa antigen and not on the 95-kDa molecule. The targets of these immunoglobulin M MAbs are not carbohydrate epitopes.
用班氏吴策线虫三期幼虫免疫后,CBA小鼠和BALB/c小鼠分别产生了多特异性和单特异性多克隆抗体反应。从免疫后的BALB/c小鼠中制备了两种单克隆抗体(MAb)。这些单克隆抗体(均为M型)识别出一种先前未描述的、在三期幼虫中高度表达的班氏吴策线虫抗原。由于在蛋白质免疫印迹法(免疫印迹)中,这些单克隆抗体不与其他九种线虫物种或两种媒介物种的抗原结合,因此它们所结合的表位似乎是班氏吴策线虫特有的。仅在一种200 kDa的抗原上鉴定出负责线虫间免疫交叉反应的磷酰胆碱表位,而在95 kDa的分子上未鉴定出。这些免疫球蛋白M单克隆抗体的靶标不是碳水化合物表位。