Dwyer J M, Parker D, Turk J L
Immunology. 1981 Apr;42(4):549-59.
Effector mechanisms that produce delayed hypersensitivity reactions to tuberculin are subject to positive immunoregulation. Two different immunoregulatory mechanisms can be demonstrated. One is specific and the other, antigenic competition, is non-specific; both are sensitive to cyclophosphamide (CY). Delayed hypersensitivity to purified protein derivative PPD in guinea-pigs can be enhanced by the administration of cyclophosphamide 3 days before but not after immunization. The enhanced response seems to result from the reduced influence on effector cells of CY-sensitive suppressor cells. Passive transfer of delayed hypersensitivity to PPD is facilitated by the use of cells from CY treated animals. The response to both immunization and skin testing with ovalbumin in animals immunized with this antigen in Freud's complete adjuvant (FCA) produces a marked, non-specific reduction in the delayed hypersensitivity response to PPD. CY given 3 days before or 1 day after immunization prevents this suppression of the PPD response by antigenic competition. The data suggests that in the generation of both the specific suppressor cells for tuberculin and the non-specific suppressor cells of antigenic competition, that can influence effector cells for tuberculin, a period of rapid cell proliferation occurs that renders both mechanisms sensitive to cyclophosphamide.
对结核菌素产生迟发型超敏反应的效应机制受到正向免疫调节。可以证明存在两种不同的免疫调节机制。一种是特异性的,另一种是抗原竞争,是非特异性的;两者都对环磷酰胺(CY)敏感。在豚鼠免疫前3天而非免疫后给予环磷酰胺,可增强其对纯化蛋白衍生物PPD的迟发型超敏反应。增强的反应似乎是由于CY敏感的抑制细胞对效应细胞的影响减弱所致。使用来自CY处理动物的细胞有助于将对PPD的迟发型超敏反应进行被动转移。在用卵白蛋白在弗氏完全佐剂(FCA)中免疫的动物中,对该抗原的免疫和皮肤试验的反应会使对PPD的迟发型超敏反应产生明显的非特异性降低。免疫前3天或免疫后1天给予CY可防止抗原竞争对PPD反应的这种抑制。数据表明,在产生结核菌素特异性抑制细胞和可影响结核菌素效应细胞的抗原竞争非特异性抑制细胞的过程中,会发生一段快速细胞增殖期,这使得两种机制都对环磷酰胺敏感。