Braun D P, Harris J E
J Natl Cancer Inst. 1981 Oct;67(4):809-14.
Leukocytes were quantitated in peripheral blood from 35 solid-tumor cancer patients and related to levels of phytohemagglutinin (PHA)-induced DNA synthesis. Levels of glass-adherent, indomethacin-sensitive, or 24-hour preculture-sensitive immunoregulatory activity were evaluated in PHA-stimulated peripheral blood mononuclear cells (PBMC). Cancer patients and patients with depressed PHA responses had significantly greater monocyte percentages in their PBMC than did healthy subjects; patients with normal PHA responses did not. Patients with disseminated disease had significantly greater monocyte percentages and depressed T-cell percentages than did controls; patients with at most minimum residual disease did not. When monocyte and lymphocyte percentages were correlated by linear regression analysis to PHA responsiveness, no significant correlation was found. A highly significant negative correlation was noted between PHA responsiveness and levels of immunoregulatory cell function. Abnormal immunoregulatory function, apart from alterations in peripheral blood leukocyte percentages and numbers contributes to impaired T-cell function in cancer patients.
对35例实体肿瘤癌症患者外周血中的白细胞进行定量分析,并将其与植物血凝素(PHA)诱导的DNA合成水平相关联。在PHA刺激的外周血单核细胞(PBMC)中评估玻璃黏附、吲哚美辛敏感或24小时预培养敏感的免疫调节活性水平。癌症患者和PHA反应低下的患者其PBMC中的单核细胞百分比显著高于健康受试者;PHA反应正常的患者则不然。患有播散性疾病的患者其单核细胞百分比显著高于对照组,T细胞百分比则低于对照组;而残留疾病最少的患者则无此差异。通过线性回归分析将单核细胞和淋巴细胞百分比与PHA反应性进行关联时,未发现显著相关性。PHA反应性与免疫调节细胞功能水平之间存在高度显著的负相关。除外周血白细胞百分比和数量的改变外,异常的免疫调节功能也导致癌症患者T细胞功能受损。