T-lymphocyte subsets in smoking and lung cancer: Analysis of monoclonal antibodies and flow cytometry.

T-lymphocyte subsets in smoking and lung cancer: Analysis of monoclonal antibodies and flow cytometry.
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吸烟和肺癌中的 T 淋巴细胞亚群:单克隆抗体和流式细胞术分析。

DOI:
10.1164/arrd.1982.126.2.265
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发表时间:
1982
期刊:
The American review of respiratory disease
影响因子:
--
通讯作者:
Kazemi,H
Kazemi,H
中科院分区:
--
文献类型:
--
作者:
Ginns,LC;Goldenheim,PD;Miller,LG;Burton,RC;Gillick,L;Colvin,RB;Goldstein,G;Kung,PC;Hurwitz,C;Kazemi,H

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为了确定免疫调节性t细胞是否在肺癌患者中发生异常,我们对26例未经治疗的肺癌患者的外周血t淋巴细胞进行了表征。将原发性鳞状癌(SC) (n = 10)、原发性腺癌(AC) (n = 7)和继发性肺转移(M) (n = 9)患者的结果相互比较,并与非癌症患者(n = 48)进行比较,包括不吸烟者(n = 29)和吸烟者(n = 19)。我们发现,在轻度至中度吸烟者中,OKT3+(成熟的外周)t淋巴细胞,包括OKT4+(诱导剂/辅助剂)和OKT8+(细胞毒性/抑制因子)淋巴细胞增加,而在重度吸烟者中,OKT4+细胞减少(p < 0.05)。反映免疫调节细胞平衡的OKT4+ / OKT8+(4/8)淋巴细胞比值在轻、中度吸烟者中正常,在重度吸烟者中下降(p < 0.05)。SC患者的循环t细胞谱与吸烟者相似。相比之下,在AC患者中,我们发现OKT8+细胞的百分比下降(p < 0.05)。AC患者的4/8比值升高(p < 0.05)。在M患者中,OKT3+细胞的比例在OKT4+和OKT8+亚群中均有所下降。M患者的4/8比例较低。因此,在吸烟者和肺癌患者中都发现了循环t细胞的一些异常。这些结果提示免疫调节异常参与肺癌的发病机制。
In order to determine whether abnormalities of immunoregulatory T-cells occur in patients with lung cancer, we characterized peripheral T-lymphocytes in 26 patients with untreated lung cancer. The results in patients with primary squamous cancer (SC) (n = 10), primary adenocarcinoma (AC) (n = 7), and secondary lung metastases (M) (n = 9) were compared with each other and to subjects without cancer (n = 48), including nonsmokers (n = 29) and smokers (n = 19). We found that OKT3+(mature, peripheral) T-lymphocytes, including both OKT4+(inducer/helper) and OKT8+(cytotoxic/suppressor) lymphocytes, were increased in light-to-moderate smokers, but that OKT4+cells were decreased in heavy smokers (p < 0.05). The ratio of OKT4+to OKT8+(4/8) lymphocytes, reflecting the balance of immunoregulatory cells, was normal in light-to-moderate smokers, but was decreased in heavy smokers (p < 0.05). The profile of circulating T-cells in patients with SC was similar to the smokers. In contrast, in patients with AC, we found a decreased percentage of OKT8+cells (p < 0.05). The 4/8 ratio was elevated in patients with AC (p < 0.05). In patients with M, there was a decreased percentage of OKT3+cells reflected in both OKT4+and OKT8+subsets. The 4/8 ratio in patients with M was low. Thus, a number of abnormalities in circulating T-cells was found both in smokers and in patients with lung cancer. These results suggest that immunoregulatory abnormalities contribute to the pathogenesis of lung cancer.