Ptak W, Skowron-Cendrzak S
Transplantation. 1977 Jul;24(1):45-51.
The cell-mediated immune responses are significantly reduced in fetal and newborn mice, furthermore, spleen cells of these animals are able to suppress the immune responses of adult lymphocytes in a variety of situations. Newborn mice sensitized to picryl chloride within 24 hr after birth fail to develop contact sensitivity reaction when tested several weeks later, and fetal mice do not develop graft-versus-host reaction when given injections of parental lymphocytes. Spleen cells of fetal or newborn mice are able to suppress the passive transfer of contact sensitivity and the local graft-versus-host reaction elicited by immunized parental cells in F1 hybrid mice, and reduce significantly the severity of graft-versus-host reaction and mortality rate in cyclophosphamide-treated F1 recipients. In no experiment were thymus cells of either fetal or newborn mice found to be inhibitory. The possible mechanisms of action and biological significance of fetal suppressor cells are discussed.
在胎儿和新生小鼠中,细胞介导的免疫反应显著降低。此外,这些动物的脾细胞在多种情况下能够抑制成年淋巴细胞的免疫反应。出生后24小时内对氯化苦基致敏的新生小鼠,在数周后进行测试时未能产生接触敏感性反应,而给胎儿小鼠注射亲代淋巴细胞时,它们不会发生移植物抗宿主反应。胎儿或新生小鼠的脾细胞能够抑制接触敏感性的被动转移以及F1杂种小鼠中免疫亲代细胞引发的局部移植物抗宿主反应,并显著降低环磷酰胺处理的F1受体中移植物抗宿主反应的严重程度和死亡率。在任何实验中,均未发现胎儿或新生小鼠的胸腺细胞具有抑制作用。本文讨论了胎儿抑制细胞可能的作用机制和生物学意义。