Bartlett G L, Kreider J W
Immunol Commun. 1981;10(8):719-31. doi: 10.3109/08820138109051958.
In order to induce specific unresponsiveness to C. parvum mice were given seven daily i.v./i.p. injections of a high dose of the vaccine, or were given a single dose i.v. injection of C. parvum followed by an i.p. injection of cyclophosphamide (CY). Mice given the high-dose procedure had a significant level of residual footpad reactivity to C. parvum challenge, but subsequent sensitizing injections did not stimulate delayed hypersensitivity (DH). In contrast, mice given C. parvum and CY did not respond to challenge, and they could not be sensitized to C. parvum. Their unresponsiveness was antigenically specific and was stable for at least six weeks. Antibodies to C. parvum were induced by both pretreatment procedures. This is the first report of the production of mice specifically unable to mount DH to a bacterial immune stimulant.
为了诱导小鼠对微小隐孢子虫产生特异性无反应性,给小鼠每日静脉内/腹腔内注射高剂量疫苗,共注射7天,或者先静脉内注射单剂量微小隐孢子虫,随后腹腔内注射环磷酰胺(CY)。接受高剂量程序的小鼠对微小隐孢子虫攻击具有显著水平的残留足垫反应性,但随后的致敏注射并未刺激迟发型超敏反应(DH)。相比之下,接受微小隐孢子虫和CY的小鼠对攻击无反应,并且它们无法被微小隐孢子虫致敏。它们的无反应性是抗原特异性的,并且至少在六周内稳定。两种预处理程序均诱导出针对微小隐孢子虫的抗体。这是首次报道产生对细菌免疫刺激物特异性无法产生迟发型超敏反应的小鼠。