Truitt G A, Rich R R, Rich S S
J Immunol. 1977 Jul;119(1):31-7.
Spleen cells obtained from BALB/c mice 4 days after allosensitization to C57BL/6 spleen cells via footpad injection suppressed the in vitro generation of BALB/c cytotoxic lymphocytes (CL) against C57BL/6 spleen cells in mixed leukocyte cultures (MLC). Suppressor activity was demonstrated by spleen cells at 4 and 7 days but not at 2, 10, or 14 days after allosensitization and was abolished by treatment with anti-Thy-1,2 serum and complement. A weak and transient cytotoxic response directed against the sensitizing alloantigen was associated with suppressor spleen cell populations, but was dissociated from suppressor function by two experimental approaches. First, increasing stimulatory cell concentration in MLC did not competitively diminish the suppressor activity; rather, the magnitude of suppression increased as the stimulatory cell concentration was increased. Second. BALB/c suppressor cells generated in vivo by either H-2b or H-2k alloantigens suppressed CL responses generated simultaneously against both alloantigens in vitro. CL responses generated against one or the other H-2 haplotype in vitro were suppressed only by suppressor cells activated by that haplotype. Therefore, splenic suppressor cells activated by alloantigen in vivo required antigen-specific restimulation in vitro; thereafter, responder cells syngeneic with the suppressor cell were rendered hyporesponsive to alloantigens by an antigen-nonspecific mechanism.
通过足垫注射对C57BL/6脾细胞进行同种致敏4天后,从BALB/c小鼠获得的脾细胞在混合淋巴细胞培养(MLC)中抑制了BALB/c细胞毒性淋巴细胞(CL)对C57BL/6脾细胞的体外生成。在同种致敏后第4天和第7天,脾细胞表现出抑制活性,但在第2天、第10天或第14天则没有,并且用抗Thy-1,2血清和补体处理后抑制活性被消除。针对致敏同种抗原的微弱且短暂的细胞毒性反应与抑制性脾细胞群体相关,但通过两种实验方法与抑制功能分离。首先,增加MLC中刺激细胞的浓度并不会竞争性地降低抑制活性;相反,随着刺激细胞浓度的增加,抑制程度会增加。其次,由H-2b或H-2k同种抗原在体内产生的BALB/c抑制细胞抑制了体外同时针对两种同种抗原产生的CL反应。体外针对一种或另一种H-2单倍型产生的CL反应仅被由该单倍型激活的抑制细胞所抑制。因此,体内被同种抗原激活的脾抑制细胞在体外需要抗原特异性再刺激;此后,与抑制细胞同基因的反应细胞通过一种抗原非特异性机制对同种抗原反应低下。