Valtonen M V, Häyry P
Infect Immun. 1978 Jan;19(1):26-8. doi: 10.1128/iai.19.1.26-28.1978.
Immunosuppression by cyclophosphamide was used to make mice incapable of B-lymphocyte responses; they could not make an antibody response to NIP-Ficoll. These mice, as well as untreated mice, were challenged intraperitoneally with graded doses of isogenic O-4,12 or O-6,7 Salmonella typhimurium derivatives. The 50% lethal dose of the O-6,7 strains was 35- to 70-fold higher than that of the O-4,12 strains, both in the normal and the immunosuppressed animals, although the latter were approximately 1,000-fold more susceptible to the infection by either challenge organism. We conclude that the O-antigen-dependent difference in the mouse virulence of these sister strains is not mediated through differences in their capacity to evoke B-lymphocyte-mediated immune responses.
使用环磷酰胺进行免疫抑制,使小鼠无法产生B淋巴细胞反应;它们无法对NIP-菲可产生抗体反应。这些小鼠以及未处理的小鼠,用不同剂量的同基因鼠伤寒沙门氏菌O-4,12或O-6,7衍生物进行腹腔注射攻击。在正常和免疫抑制的动物中,O-6,7菌株的50%致死剂量比O-4,12菌株高35至70倍,尽管后者对任何一种攻击菌株的感染敏感性大约高1000倍。我们得出结论,这些姐妹菌株在小鼠毒力方面的O抗原依赖性差异不是通过它们诱发B淋巴细胞介导的免疫反应能力的差异来介导的。