Iwasaki T, Hallam J A, Joseph L J, Shearer G M
J Immunol. 1987 Jun 1;138(11):3604-10.
A severe, antigen-nonspecific, and long-lasting immune-deficient state can be induced in healthy, adult immune-competent F1 hybrid mice by a single i.v. injection of parental T lymphocytes. The present report demonstrates that this graft-vs-host-induced immune deficiency (GVHID) can be prevented in an antigen-specific way by immunization of the F1 mice with allogeneic cells before induction of GVHID. Thus, spleen cells from (A X B)F1 mice primed with allogeneic cells from strain C and then injected with parental spleen cells from A did not generate cytotoxic T lymphocyte responses to trinitophenyl-modified self cells or to allogeneic cells from third party strains D or E. However, spleen cells from the same mice generated normal levels of cytotoxic T lymphocyte activity to allogeneic cells from C, the strain used for immunization. Furthermore, mice exposed to murine cytomegalovirus before induction of GVHID were resistant to a subsequent challenge with murine cytomegalovirus, whereas GVHID mice that received only the murine cytomegalovirus challenge all died. These findings are discussed with respect to the possibilities that primed and unprimed T helper cells may be differentially susceptible to the suppressive effects of GVH.
通过静脉内单次注射亲代T淋巴细胞,可在健康的成年具有免疫能力的F1杂种小鼠中诱导出一种严重的、抗原非特异性的、持久的免疫缺陷状态。本报告表明,在诱导移植物抗宿主诱导的免疫缺陷(GVHID)之前,用同种异体细胞免疫F1小鼠,可以以抗原特异性的方式预防这种情况。因此,先用来自C品系的同种异体细胞致敏,然后注射来自A的亲代脾细胞的(A×B)F1小鼠的脾细胞,不会对三硝基苯基修饰的自身细胞或来自第三方品系D或E的同种异体细胞产生细胞毒性T淋巴细胞反应。然而,来自相同小鼠的脾细胞对来自用于免疫的C品系的同种异体细胞产生正常水平的细胞毒性T淋巴细胞活性。此外,在诱导GVHID之前暴露于鼠巨细胞病毒的小鼠对随后的鼠巨细胞病毒攻击具有抗性,而仅接受鼠巨细胞病毒攻击的GVHID小鼠全部死亡。就致敏和未致敏的T辅助细胞可能对GVH的抑制作用有不同敏感性的可能性进行了讨论。