Elkins W L, Pickard A, Pierson G R
Cancer Immunol Immunother. 1984;18(2):91-100. doi: 10.1007/BF00205741.
Leukemic cells from the blood and marrow of 25 cases of newly diagnosed acute leukemia were presented as target cells to alloreactive effector cells from unrelated normal donors in cell-mediated cytotoxicity assays. In three cases the leukemic targets were poorly killed relative to nonleukemic, HLA-identical target cells. The poor killing of the leukemic cells from one of these cases was shown by competitive inhibition to be due to deficient expression of normal class-I HLA antigens rather than resistance to lysis. Furthermore, the leukemic cells from these three patients were also deficient in binding monoclonal antibodies to nonpolymorphic determinants of class-I HLA and B2 microglobulin. Two additional cases were identified as having a less extensive deficit of HLA, and may be representative of a group with relatively subtle changes in these cell surface antigens. The possible significance of reduced expression of HLA in leukemic progression and in susceptibility to graft-vs-leukemia reactions after bone marrow transplantation is discussed.
在细胞介导的细胞毒性试验中,将25例新诊断急性白血病患者血液和骨髓中的白血病细胞作为靶细胞,与来自无关正常供体的同种异体反应性效应细胞进行反应。在3例患者中,相对于非白血病、HLA相同的靶细胞,白血病靶细胞的杀伤效果较差。其中1例患者白血病细胞杀伤效果差,通过竞争性抑制试验表明,这是由于正常I类HLA抗原表达缺陷,而非对裂解有抗性。此外,这3例患者的白血病细胞与针对I类HLA和β2微球蛋白非多态性决定簇的单克隆抗体结合也存在缺陷。另外2例患者被确定为HLA缺陷程度较轻,可能代表了一组细胞表面抗原发生相对细微变化的患者群体。本文讨论了HLA表达降低在白血病进展以及骨髓移植后移植物抗白血病反应易感性方面的可能意义。