Welsh K I, Dorval G, Nilsson K, Clements G B, Wigzell H
Scand J Immunol. 1977;6(4):265-71. doi: 10.1111/j.1365-3083.1977.tb00393.x.
Beta2-microglobulin (beta2m) participates as an integral part in molecules of the major histocompatibility complex (MHC) type. Absence of beta2m makes the residual heavy MHC chain largely inactive as antigen. Striking reductions in the density per unit surface area of beta2m in seven out of nine malignant lymphoid tumour lines in comparison with normal lymphocytes or "immortalized" Epstein-Barr-virus-transformed lymphoblastoid lines were found is this study. This would seemingly represent a specific reduction in the ability of the malignant cells to express actively produced beta2m, since their HLA antigenic determinants were not reduced to the same extent and no indications were obtained suggesting that free beta2m could transfer from one cell to another. However, that beta2m is important in conveying serological specificities of MHC type to cells was shown by fusion of beta2m-negative and beta2m-positive cells, yielding hybrid cells with synergistically increased numbers of detectable, HLA-related determinants. Whether the reduction of beta2m on malignant versus nonmalignant lymphoid cells bears any relevance as to emergence of the malignant clones and resistance to possible anti-tumour reactions would now be an issue for study.
β2-微球蛋白(β2m)作为主要组织相容性复合体(MHC)类型分子的一个组成部分发挥作用。β2m的缺失会使剩余的重链MHC作为抗原基本失去活性。在本研究中发现,与正常淋巴细胞或“永生化”的爱泼斯坦-巴尔病毒转化的淋巴母细胞系相比,9种恶性淋巴瘤细胞系中有7种的β2m单位表面积密度显著降低。这似乎代表恶性细胞主动表达β2m的能力出现了特异性降低,因为它们的HLA抗原决定簇并没有降低到相同程度,也没有迹象表明游离的β2m可以从一个细胞转移到另一个细胞。然而,β2m阴性细胞和β2m阳性细胞的融合产生了具有协同增加数量的可检测的HLA相关决定簇的杂交细胞,这表明β2m在将MHC类型的血清学特异性传递给细胞方面很重要。恶性与非恶性淋巴细胞上β2m的减少是否与恶性克隆的出现以及对可能的抗肿瘤反应的抗性有关,现在将是一个研究问题。