Gautam S C, Beckman K D, Wong H L, Battisto J R
Cell Immunol. 1984 Aug;87(1):23-34. doi: 10.1016/0008-8749(84)90127-8.
Two suppressor cell populations that interact to down-regulate in vivo development of the cytolytic T-cell (CTL) response to trinitrophenyl-modified syngeneic spleen cells (TNP-SC) have been further characterized. Suppressor cells induced by the iv injection of trinitrophenyl-modified syngeneic spleen cells possess Thy 1.2 antigen. Their precursors are insensitive to pretreatment of host animals with cyclophosphamide (CY). Suppressor cells that arise after dermal sensitization with trinitrochlorobenzene are also Thy 1.2 antigen positive but their precursors are sensitive to pretreatment with CY. These characteristics of the two suppressor T cells (Ts) are identical to those of the two Ts that are generated by similar methodologies and that together suppress contact sensitivity (CS) to picryl chloride. Neither the CS nor CTL response was suppressed when host animals possessed only one set of Ts. In contrast to suppression of CS at the efferent phase, development of CTL was suppressed only when the two Ts were present early during sensitization (afferent phase). Since the results point to several similarities between the two sets of Ts that are active in the down-regulation of the CS and CTL responses, it is suggested that the two dissimilar immune responses directed to the same hapten, namely CS and CTL, may be controlled by the same suppressor cells. Since it appears that the two sets of Ts interact to affect different phases of the CS and CTL responses, down-regulation of each must be accomplished through different mechanisms.
两种相互作用以下调对三硝基苯修饰的同基因脾细胞(TNP-SC)的细胞毒性T细胞(CTL)应答的体内发育的抑制细胞群体已得到进一步表征。经静脉注射三硝基苯修饰的同基因脾细胞诱导产生的抑制细胞具有Thy 1.2抗原。它们的前体对用环磷酰胺(CY)预处理宿主动物不敏感。经三硝基氯苯皮肤致敏后产生的抑制细胞也为Thy 1.2抗原阳性,但其前体对CY预处理敏感。这两种抑制性T细胞(Ts)的这些特征与通过类似方法产生且共同抑制对苦味酰氯的接触敏感性(CS)的两种Ts的特征相同。当宿主动物仅拥有一组Ts时,CS和CTL应答均未受到抑制。与在传出阶段抑制CS相反,仅当两种Ts在致敏早期(传入阶段)存在时,CTL的发育才受到抑制。由于结果表明在下调CS和CTL应答中起作用的两组Ts之间存在若干相似性,因此表明针对同一半抗原的两种不同免疫应答,即CS和CTL,可能由相同的抑制细胞控制。由于似乎两组Ts相互作用以影响CS和CTL应答的不同阶段,因此每种应答的下调必须通过不同机制来完成。