Sato H, Diena B B, Greenberg L
Bull World Health Organ. 1967;37(6):973-81.
The authors have attempted to prepare lysed BCG vaccines retaining the protective antigens of the BCG cell wall and yet eliciting in experimental animals limited sensitivity to the tuberculin substances, the advantage sought being to retain the usefulness of the tuberculin following vaccination as an indicator of superinfection.Experimental vaccines were prepared by growing and lysing BCG in both Dubos and Aldridge liquid media with glycine, lysosyme and lithium chloride; vaccines were also prepared by autolysis in Aldridge nitrogen-deficient, chemically defined medium.Glycine, lysozyme and lithium chloride significantly reduced both the protective and allergenic properties of the lysates. The best protection was afforded by BCG cells autolysed in Aldridge medium. Treatment of the BCG autolysates with lysozyme alone did not affect the protective capability of the vaccines and almost completely eliminated the allergenicity. It is suggested that these BCG lysates contain metabolically inactive cells, which do not multiply in vitro but may still provide sufficient antigen in vivo to ensure protection.
作者们试图制备经裂解的卡介苗疫苗,保留卡介苗细胞壁的保护性抗原,同时使实验动物对结核菌素物质的敏感性受限,这样做所追求的优势是在接种疫苗后保留结核菌素作为再感染指标的效用。通过在杜博斯和奥尔德里奇液体培养基中利用甘氨酸、溶菌酶和氯化锂培养并裂解卡介苗来制备实验性疫苗;疫苗也通过在奥尔德里奇缺氮化学限定培养基中自溶来制备。甘氨酸、溶菌酶和氯化锂显著降低了裂解物的保护和致敏特性。在奥尔德里奇培养基中自溶的卡介苗细胞提供了最佳保护。仅用溶菌酶处理卡介苗自溶物不影响疫苗的保护能力,且几乎完全消除了致敏性。有人提出,这些卡介苗裂解物含有代谢不活跃的细胞,这些细胞在体外不增殖,但在体内仍可能提供足够的抗原以确保保护作用。