Tursunov S S, Shchetkin V Iu
Med Parazitol (Mosk). 1994 Oct-Dec(4):23-6.
The authors describe a procedure for producing the antigen by using a promastigotic suspension of the high-virulent inoculative strain Leishmania major. A Leishmania culture medium was improved to enhance the yield of parasites up to 1-3 billion cells in a flask. The grown culture was washed off with isotonic sodium chloride solution, from the medium residues and concentrated up to 1 billion cells per ml of the cvolume. The cell concentrate contained no rabbit blood additive, as evidenced by the gel double diffusion test. The combinations of destruction via multiple freezing-unfreezing or lyophilization, followed by ultrasound treatment were found to be the best modes of promastigotic disintegration. The antigenic suspension generally displayed 3-5 precipitation lines with hyperimmune rabbit sera and 1-3 precipitation lines with sera from the infected animals. The number of precipitation lines is higher in the suspension from the high-virulent Leishmania strains. Fractions of protective antigens have not been detected so far.
作者描述了一种通过使用高毒力接种株硕大利什曼原虫的前鞭毛体悬液来制备抗原的方法。对利什曼原虫培养基进行了改进,以提高烧瓶中寄生虫产量,使其达到10亿至30亿个细胞。将生长的培养物用等渗氯化钠溶液从培养基残渣中冲洗掉,并浓缩至每毫升体积含10亿个细胞。凝胶双向扩散试验证明,细胞浓缩物中不含兔血添加剂。发现通过多次冻融或冻干破坏,随后进行超声处理的组合是前鞭毛体解体的最佳方式。抗原悬液通常与超免疫兔血清显示3 - 5条沉淀线,与感染动物的血清显示1 - 3条沉淀线。来自高毒力利什曼原虫菌株的悬液中沉淀线的数量更多。到目前为止,尚未检测到保护性抗原组分。