Flexman J P, Shellam G R
Br J Cancer. 1980 Jul;42(1):41-51. doi: 10.1038/bjc.1980.201.
Differences were seen in the ability of 2 strains of C. parvum to augment cytotoxicity attributable to NK cells towards a rat lymphoma. Furthermore, 2 batches of the same strain of C. parvum prepared by different methods also differed in their ability to augment cytotoxicity. Other factors influencing cytotoxicity were dose, route of inoculation and time after injection at which the assay was performed. Although all preparations of C. parvum augmented the cytotoxicity of peritoneal-exudate cells when injected i.p., only the most stimulatory preparation consistently augmented splenic cytotoxicity when given by this route. I.v. administration of 1 mg of C. parvum produced peak levels of splenic cytotoxicity 2-3 days later, but this response was strictly dose-dependent, since 1 microgram depressed splenic cytotoxicity. This dose-dependent effect also extended to ADCC, since 1 mg stimulated cytotoxicity towards antibody-coated P815 cells, whilst 1 microgram depressed it in a manner similar to its effect on natural cytotoxicity. Whilst the cytotoxic cells of stimulated rats closely resembled the NK cells of normal rats, BN rats responded differently to C. parvum from W/Fu or WAG rats, in that marked lysis of P815 or RBL-5 cells was observed, though these targets are usually resistant to lysis by rat NK cells in short-term assays.
两株微小隐孢子虫增强自然杀伤细胞对大鼠淋巴瘤细胞毒性的能力存在差异。此外,用不同方法制备的同一株微小隐孢子虫的两批产品在增强细胞毒性的能力上也有所不同。影响细胞毒性的其他因素包括剂量、接种途径以及进行检测时注射后的时间。尽管所有微小隐孢子虫制剂经腹腔注射后都能增强腹腔渗出细胞的细胞毒性,但只有最具刺激作用的制剂经该途径给药时能持续增强脾细胞毒性。静脉注射1毫克微小隐孢子虫2 - 3天后可使脾细胞毒性达到峰值水平,但这种反应严格依赖剂量,因为1微克会降低脾细胞毒性。这种剂量依赖性效应也扩展到抗体依赖的细胞介导的细胞毒性(ADCC),因为1毫克刺激对抗体包被的P815细胞的细胞毒性,而1微克则以类似于其对自然细胞毒性的作用方式降低这种毒性。虽然受刺激大鼠的细胞毒性细胞与正常大鼠的自然杀伤细胞非常相似,但BN大鼠对微小隐孢子虫的反应与W/Fu或WAG大鼠不同,即观察到对P815或RBL - 5细胞的明显裂解,尽管在短期检测中这些靶细胞通常对大鼠自然杀伤细胞的裂解具有抗性。