Riggs M W, Cama V A, Leary H L, Sterling C R
Department of Veterinary Science, University of Arizona, Tucson 85721.
Infect Immun. 1994 May;62(5):1927-39. doi: 10.1128/iai.62.5.1927-1939.1994.
Control of cryptosporidiosis is currently hampered by the absence of drugs or vaccines proven consistently effective against Cryptosporidium parvum. On the basis of observations that anti-C. parvum antibody has therapeutic effect against cryptosporidiosis, cows were immunized with C. parvum to produce hyperimmune colostral antibody. An antibody-rich fraction was prepared and differentiated from control (nonhyperimmune) antibody by enzyme-linked immunosorbent assay, immunofluorescence assay, immunoelectron microscopy, and in vitro neutralizing titer against DEAE-cellulose-isolated C. parvum sporozoites. Oocyst, purified sporozoite, and merozoite antigens recognized by hyperimmune antibody were defined by Western blot (immunoblot). Hyperimmune antibody recognized antigens common to oocysts, sporozoites, and merozoites, as well as stage-specific antigens. Upon incubation with hyperimmune antibody, sporozoites underwent distinct morphologic changes characterized by progressive formation and eventual release of membranous sporozoite surface antigen-antibody complexes, similar to the malaria circumsporozoite precipitate reaction. The infectivity of sporozoites having undergone this reaction was neutralized. The reaction was minimal or absent on sporozoites incubated with control antibody. To determine therapeutic effect in vivo, persistent C. parvum infection was established in adult severe combined immune-deficient (SCID) mice by oral inoculation with 10(7) oocysts. At 5 weeks postinfection, infected mice were treated for 10 days with hyperimmune or control antibody by inclusion in drinking water and daily gavage. Fecal oocyst shedding and infection scores in the gastrointestinal tract and gall bladder/common bile duct in hyperimmune antibody-treated mice were significantly lower than those in the control antibody-treated mice. Hyperimmune bovine antibody prepared against C. parvum may provide a first-generation therapy for control of cryptosporidiosis. Additionally, the defined antigens can be evaluated as subunit immunogens to produce better-characterized polyclonal antibody for control of cryptosporidiosis or as targets for monoclonal antibody-based immunotherapy.
目前,由于缺乏经证实对微小隐孢子虫持续有效的药物或疫苗,隐孢子虫病的控制受到阻碍。基于抗微小隐孢子虫抗体对隐孢子虫病具有治疗作用的观察结果,用微小隐孢子虫对奶牛进行免疫以产生超免疫初乳抗体。制备了富含抗体的组分,并通过酶联免疫吸附测定、免疫荧光测定、免疫电子显微镜以及针对DEAE - 纤维素分离的微小隐孢子虫子孢子的体外中和效价,将其与对照(非超免疫)抗体区分开来。通过蛋白质印迹法(免疫印迹)确定超免疫抗体识别的卵囊、纯化子孢子和裂殖子抗原。超免疫抗体识别卵囊、子孢子和裂殖子共有的抗原以及阶段特异性抗原。与超免疫抗体孵育后,子孢子经历了明显的形态学变化,其特征是膜性子孢子表面抗原 - 抗体复合物逐渐形成并最终释放,类似于疟疾环子孢子沉淀反应。经历此反应的子孢子的感染性被中和。与对照抗体孵育的子孢子上该反应极小或不存在。为了确定体内治疗效果,通过口服接种10^7个卵囊,在成年重度联合免疫缺陷(SCID)小鼠中建立持续性微小隐孢子虫感染。在感染后5周,通过将超免疫或对照抗体加入饮用水中并每日灌胃,对感染小鼠进行10天的治疗。超免疫抗体治疗的小鼠粪便中卵囊排出量以及胃肠道和胆囊/胆总管中的感染评分显著低于对照抗体治疗的小鼠。针对微小隐孢子虫制备的超免疫牛抗体可为隐孢子虫病的控制提供第一代治疗方法。此外,确定的抗原可作为亚单位免疫原进行评估,以产生特性更好的多克隆抗体用于控制隐孢子虫病,或作为基于单克隆抗体的免疫治疗的靶点。