Nanduri J, Kazura J W
Department of Medicine, Case Western Reserve University, Cleveland, OH 44106.
J Immunol. 1989 Nov 15;143(10):3359-63.
Progress in development of a vaccine against human filariasis has been hampered by lack of knowledge of the biochemical structure of specific Ag that induce protective immunity in experimental hosts. In the current study, antiserum to infective third-stage larvae of Brugia malayi was used to select potentially protective Ag shared by microfilariae (mf) and adult worms. A major Ag of 97 kDa (Bm 97) was identified by immunoblotting and isolated by electroelution. Immunization of mice with 2 micrograms electroeluted Bm 97 induced partial resistance to subsequent i.v. challenge with live B. malayi mf (40 to 60% reduction in parasitemia compared to controls, p less than 0.05). Immunoblot studies of B. malayi mf and adult worm lysates showed reactivity of a 97-kDa molecule with monospecific antiserum to Schistosoma mansoni paramyosin. In addition, mouse antibody to Bm 97 reacted with a 97-kDa molecule contained in wild-type Caenorhabditis elegans but not in two mutant strains deficient for paramyosin. Subcutaneous injection of mice with paramyosin (5 micrograms twice at a 2-wk interval) purified from C. elegans or B. malayi by salt precipitation induced resistance to microfilaremia (21 to 60% lower intensities than controls, p less than 0.01). These data indicate that the invertebrate muscle protein paramyosin enhances clearance of blood-borne stages of lymphatic filariae. Examination of the ability of paramyosin to induce resistance in third-stage larvae-challenged hosts is warranted.
针对人类丝虫病疫苗研发的进展,因缺乏对能在实验宿主中诱导保护性免疫的特定抗原生化结构的了解而受阻。在当前研究中,使用针对马来布鲁线虫感染性三期幼虫的抗血清来筛选微丝蚴(mf)和成虫共有的潜在保护性抗原。通过免疫印迹鉴定出一种97 kDa的主要抗原(Bm 97),并通过电洗脱法分离出来。用2微克电洗脱的Bm 97免疫小鼠,可诱导对随后静脉注射活的马来布鲁线虫mf产生部分抗性(与对照组相比,虫血症降低40%至60%,p<0.05)。对马来布鲁线虫mf和成虫裂解物的免疫印迹研究表明,一种97 kDa分子与曼氏血吸虫副肌球蛋白的单特异性抗血清发生反应。此外,小鼠针对Bm 97的抗体与野生型秀丽隐杆线虫中含有的一种97 kDa分子发生反应,但在两种缺乏副肌球蛋白的突变株中未发生反应。通过盐沉淀从秀丽隐杆线虫或马来布鲁线虫中纯化的副肌球蛋白(5微克,每隔2周注射两次)皮下注射小鼠,可诱导对微丝蚴血症产生抗性(强度比对照组低21%至60%,p<0.01)。这些数据表明,无脊椎动物肌肉蛋白副肌球蛋白可增强淋巴丝虫血源期的清除。有必要研究副肌球蛋白在三期幼虫攻击宿主中诱导抗性的能力。