Efremidis A P, Haubenstock H S, Papadopoulos N M, Holland J F, Bekesi J G
J Immunopharmacol. 1986;8(2):129-44. doi: 10.3109/08923978609028612.
Immunological and biochemical markers of leukemia/lymphoma cells have provided valuable insight into hematopoietic malignancy and normal differentiation. The general assumption is that as early lymphoid cells become committed towards terminal differentiation they lose their capacity for bimodal differentiation and cells become restricted to B or T cell development and function. We have observed that phenotypically "late" leukemic B cells close to secretory stage can spontaneously express mature T cell antigens (T11, T4 and T8) after culture in vitro. In further studies of these cells, it was found that the biochemical marker lactate Dehydrogenase (LD) follows the intermediate pattern expressed by thymocytes rather than that of typical B cells. The expression of T cell antigens can be blocked by incubating these cells with the phorbol ester TPA (12-0-tetradecanoyl phorbol 13 acetate) which promotes unidirectional B cell maturation to plasmacytoid cells in a way that mimics normal B cell differentiation. These observations indicate that presecretory malignant B cells are still programmed to express T cell biochemical and antigenic markers and this expression can be influenced by environmental conditions in vitro.
白血病/淋巴瘤细胞的免疫和生化标志物为造血系统恶性肿瘤及正常分化提供了有价值的见解。一般认为,随着早期淋巴细胞向终末分化发展,它们失去了双峰分化的能力,细胞局限于B细胞或T细胞的发育和功能。我们观察到,表型上接近分泌阶段的“晚期”白血病B细胞在体外培养后可自发表达成熟T细胞抗原(T11、T4和T8)。在对这些细胞的进一步研究中发现,生化标志物乳酸脱氢酶(LD)呈现胸腺细胞表达的中间模式,而非典型B细胞的模式。通过用佛波酯TPA(12 - O - 十四酰佛波醇13 - 乙酸酯)孵育这些细胞,可阻断T细胞抗原的表达,TPA以模拟正常B细胞分化的方式促进B细胞单向成熟为浆细胞样细胞。这些观察结果表明,分泌前的恶性B细胞仍被编程表达T细胞生化和抗原标志物,且这种表达可受体外环境条件的影响。