Crosier P S
Aust N Z J Med. 1986 Jun;16(3):389-92. doi: 10.1111/j.1445-5994.1986.tb01194.x.
Surface membrane studies of cells from a patient with T-cell chronic lymphocytic leukemia (T-CLL) showed that they had an OKT3+, OKT4-, OKT8+ phenotype which is consistent with the phenotype of normal circulating peripheral blood suppressor/cytotoxic T-lymphocytes. The cells were HLA-DR+, anti-Tac-, SmIg- and E rosette+. Parallel studies in vitro showed that the T-CLL cells had a marked suppressive effect on both the mixed lymphocyte culture (MLC) proliferative response and the activation of cytotoxic T-lymphocytes. The T-CLL cells failed to respond or stimulate in MLC and were not directly cytotoxic to allogeneic peripheral blood lymphocyte targets. Both the suppression of the MLC and the cytotoxic responses depended on the presence of the T-CLL cells and not T-CLL culture supernatants. The T-CLL cells did not suppress the production of polyclonal antibody and did not produce interleukin-2 to levels above normal control lymphocytes.
对一名T细胞慢性淋巴细胞白血病(T-CLL)患者的细胞进行的表面膜研究表明,这些细胞具有OKT3 +、OKT4 -、OKT8 +表型,这与正常循环外周血抑制/细胞毒性T淋巴细胞的表型一致。这些细胞HLA-DR +、抗Tac -、SmIg -且E花环阳性。体外平行研究表明,T-CLL细胞对混合淋巴细胞培养(MLC)增殖反应和细胞毒性T淋巴细胞的激活均具有显著的抑制作用。T-CLL细胞在MLC中无反应或不刺激,并且对异基因外周血淋巴细胞靶标无直接细胞毒性。MLC的抑制和细胞毒性反应均取决于T-CLL细胞的存在,而非T-CLL培养上清液。T-CLL细胞不抑制多克隆抗体的产生,且产生的白细胞介素-2水平未高于正常对照淋巴细胞。