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缓解期淋巴细胞对自身白血病成髓细胞的反应。

Response of remission lymphocytes to autochthonous leukaemic myeloblasts.

作者信息

Taylor G M, Freeman C B, Harris R

出版信息

Br J Cancer. 1976 May;33(5):501-11. doi: 10.1038/bjc.1976.81.

Abstract

Thymidine incorporation in vitro by remission lymphocytes from a total of 6 patients with acute myeloid leukaemia (AML) was measured following stimulation by autochthonous and allogeneic AML blasts and cell lines. The early peak response to autochthonous blasts in 2 of these patients (48-72 h) is consistent with the concept of a population of lymphocytes pre-immunized to antigens carried by the blasts. Although stimulation in one patient was increased in the presence of more stimulating (S) blasts than responding (R) lymphocytes, positive responses in other tests were obtained at an S : R ratio of 1 : 1-5. When different methods of treatment of the stimulating autochthonous blasts were compared with untreated cells, mitomycin C gave the highest stimulation indices 2 out of 3 tests. Tissue culture medium in which autochthonous blasts had been incubated for 3-5 days failed to stimulate either remission lymphocytes alone, or combined cultures of lymphocytes with autochthonous or allogeneic blasts, suggesting that mitogenic factors released from autochthonous blasts are not responsible for lymphocyte stimulation. Treatment of autochthonous or allogeneic AML blasts with glycine-HC1(pH 3-0) to remove putative "blocking" factors failed to increase the stimulatory capacity of the leukaemic blasts.

摘要

在自体和同种异体急性髓系白血病(AML)原始细胞及细胞系的刺激下,对总共6例急性髓系白血病患者缓解期淋巴细胞的体外胸苷掺入情况进行了测定。其中2例患者对自体原始细胞的早期峰值反应(48 - 72小时)与对原始细胞携带抗原预先免疫的淋巴细胞群体概念相符。尽管在一名患者中,当刺激(S)原始细胞比反应(R)淋巴细胞多时刺激增强,但在其他试验中,当S:R比例为1:1 - 5时获得了阳性反应。当将刺激自体原始细胞的不同处理方法与未处理细胞进行比较时,在3次试验中的2次,丝裂霉素C给出了最高的刺激指数。曾在其中孵育过3 - 5天自体原始细胞的组织培养基,单独刺激缓解期淋巴细胞或淋巴细胞与自体或同种异体原始细胞的联合培养物均未成功,这表明从自体原始细胞释放的促有丝分裂因子并非淋巴细胞刺激的原因。用甘氨酸 - 盐酸(pH 3.0)处理自体或同种异体AML原始细胞以去除假定的“阻断”因子,并未增加白血病原始细胞的刺激能力。

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Human leukemia-associated anti-nuclear reactivity.人类白血病相关的抗核反应性。
Proc Natl Acad Sci U S A. 1974 Mar;71(3):685-9. doi: 10.1073/pnas.71.3.685.

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