Halper J P, Fu S M, Gottlieb A B, Winchester R J, Kunkel H G
J Clin Invest. 1979 Nov;64(5):1141-8. doi: 10.1172/JCI109567.
The human Ia-like antigens, selectively expressed on B lymphocytes, are now recognized to be closely associated with, or identical to, the gene products of the major histocompatibility complex responsible for stimulation in the mixed lymphocyte reaction. The leukemic B lymphocytes of patients with chronic lymphocytic leukemia express these antigens very well. In the present study they were readily detected by several techniques utilizing both allo- and heteroantisera. However, the leukemic B cells from most patients were found to be extremely poor stimulating cells in the mixed lymphocyte reaction. This was particularly apparent when comparisons were made on a B-cell basis with isolated normal B lymphocytes. Leukemic cell death, abnormal kinetics of leukemic cell-mediated stimulation, and serum or cellular suppressor factors do not appear to explain these findings. Studies comparing cells from a leukemic patient with those of her HLA identical sibling and results of mixed lymphocyte reactions between normal and leukemic subjects discordant for D-region-associated Ia antigens ruled out genetic explanations for the differences observed. Experiments with normal peripheral blood mononuclear cells depleted of T cells and monocytes exclude the quantitative deficiency of monocytes which is found in the peripheral blood of most leukemic patients as an explanation. The present results with chronic lymphocytic leukemia cells indicate that the mere expression of the Ia-like antigens by cell populations does not render them effective stimulators. The accumulated evidence obtained indicate that abnormalities, particularly of membrane function and metabolism, known to occur in chronic lymphocytic leukemia lymphocytes may be involved in the poor stimulatory capacity of the leukemic B cells.
人类Ia样抗原选择性地表达于B淋巴细胞,目前已认识到它们与主要组织相容性复合体的基因产物密切相关或完全相同,该复合体的基因产物在混合淋巴细胞反应中负责刺激作用。慢性淋巴细胞白血病患者的白血病B淋巴细胞能很好地表达这些抗原。在本研究中,利用同种异体和异种抗血清的几种技术很容易检测到它们。然而,发现大多数患者的白血病B细胞在混合淋巴细胞反应中是极弱的刺激细胞。当与分离的正常B淋巴细胞在B细胞基础上进行比较时,这一点尤为明显。白血病细胞死亡、白血病细胞介导的刺激的异常动力学以及血清或细胞抑制因子似乎都不能解释这些发现。将白血病患者的细胞与其HLA相同的同胞的细胞进行比较,以及对D区相关Ia抗原不一致的正常人和白血病患者之间的混合淋巴细胞反应结果,排除了对所观察到的差异的遗传学解释。用去除了T细胞和单核细胞的正常外周血单个核细胞进行的实验排除了大多数白血病患者外周血中存在的单核细胞数量不足作为解释。目前关于慢性淋巴细胞白血病细胞的结果表明,细胞群体仅仅表达Ia样抗原并不能使其成为有效的刺激细胞。所获得的累积证据表明,已知发生在慢性淋巴细胞白血病淋巴细胞中的异常,特别是膜功能和代谢异常,可能与白血病B细胞的弱刺激能力有关。