Speirs R, Benson R W, Schiffman G
J Environ Pathol Toxicol. 1978 May-Jun;1(5):689-99.
This study characterizes the response of BALB/c mice to Type III pneumococcal polysaccharides (S3) administered alone or with a vaccine consisting of diphtheria toxoid, pertussis vaccine, and tetanus toxoid (DPT). The usefulness of this vaccine in toxicological protocols for determining immunocompetence is discussed. There were significant differences in antibody titers depending upon the route of injection and whether the S3 was administered in saline or mixed with DPT. Subcutaneous injections induced higher antibody titers to S3 than did intraperitoneal injections. The effect of DPT varied depending upon the manner of administration. Subcutaneous injections of DPT mixed with S3 increased the S3 antibody titers to a dose of 0.1 microgram S3, but had little or no effect at 0.25, 0.5, and 0.75 microgram. Antibody titers were suppressed only at the highest dose administered (1.0 microgram). On the other hand, when administered intraperitoneally DPT has a consistently suppressive effect on 5 day peak S3 antibody titers. Intraperitoneal injections of DPT appeared to delay the rate of antibody induction, since antibody titers at 14 and 21 days were higher in the DPT treated mice than in those animals receiving S3 alone.
本研究描述了BALB/c小鼠对单独给予的III型肺炎球菌多糖(S3)或与由白喉类毒素、百日咳疫苗和破伤风类毒素组成的疫苗(DPT)联合给予时的反应。讨论了这种疫苗在确定免疫能力的毒理学实验方案中的实用性。根据注射途径以及S3是用生理盐水给药还是与DPT混合给药,抗体滴度存在显著差异。皮下注射诱导的S3抗体滴度高于腹腔注射。DPT的效果因给药方式而异。皮下注射与S3混合的DPT可使S3抗体滴度在S3剂量为0.1微克时升高,但在0.25、0.5和0.75微克时几乎没有影响或没有影响。抗体滴度仅在最高给药剂量(1.0微克)时受到抑制。另一方面,当腹腔注射时,DPT对第5天的S3抗体滴度峰值始终具有抑制作用。腹腔注射DPT似乎延迟了抗体诱导速率,因为在第14天和第21天,接受DPT治疗的小鼠的抗体滴度高于仅接受S3的动物。