Cui Ming, Wang Shan, Ye Ying-Jiang, Cui Zhi-Rong, Ke Yang
Department of Gastroenterological Surgery, Peking University People's Hospital, Beijing, China.
Zhonghua Yi Xue Za Zhi. 2007 Jan 2;87(1):16-9.
To analyze the effect of tumor burden on the differentiation of T1 and T2 cells and its implication in patients with colorectal cancer.
Peripheral venous blood samples were obtained from 20 patients with primary colorectal cancer before and 7 days after the operation, radical operation in 17 patients and palliative resection in 3 patients. Twenty sex and age-matched patients with benign diseases treated in the same period were used as controls. T1 and T2 cells in the peripheral blood were evaluated by detecting the intracellular interferon-gamma and interleukin-4 production with 4-color flow cytometry. Lymphocyte subsets in the peripheral blood were also measured by flow cytometry.
At the time of diagnosis, the percentage of T1 and T2 cells in the peripheral lymphocytes of the case group was lower significantly than that of the control group (P = 0.006, and P = 0.017). There was no significant difference in the T, CD4(+) T, CD8(+) T, B, and NK cells between the two groups. After getting rid of the tumor burden, the percentage of T1 cells increased, however, not significantly (P > 0.05). And the percentage of T2 cells increased significantly (P = 0.020). The percentages of T1 cell of the patients with the tumor > or = 5 cm and of the patients with poorly differentiated tumors were significantly lower than those of the patients with the tumor < 5 cm and of the patients with well or moderately differentiated tumors (P = 0.064, and P = 0.072). The percentage of T1 cells in the patients with lymph node metastasis and stage III approximately IV tumor were lower significantly than those of the patients without lymph node metastasis and those with stage I approximately II tumor (P = 0.033 and P = 0.033). No significant differences were found between the population of T1 cells and such factors as tumor size, serosa invasion, and distant metastasis.
Tumor load suppresses the differentiation of T1 and T2 cells in the patients with colorectal cancer significantly, and may be an important factor in the development of immunosuppression. After getting rid of the tumor burden, the percentages of T1 and T2 increase in a short time, and the immunologic function is improved. Determination of T1 may be helpful to indicate the prognosis of colorectal cancer.
分析肿瘤负荷对T1和T2细胞分化的影响及其在结直肠癌患者中的意义。
采集20例原发性结直肠癌患者手术前及术后7天的外周静脉血样本,其中17例行根治性手术,3例行姑息性切除。同期选取20例年龄和性别匹配的良性疾病患者作为对照。采用四色流式细胞术检测外周血中细胞内γ干扰素和白细胞介素-4的产生,评估外周血中的T1和T2细胞。同时用流式细胞术检测外周血淋巴细胞亚群。
诊断时,病例组外周淋巴细胞中T1和T2细胞的百分比显著低于对照组(P = 0.006,P = 0.017)。两组间T、CD4(+)T、CD8(+)T、B和NK细胞无显著差异。去除肿瘤负荷后,T1细胞百分比升高,但差异不显著(P > 0.05),而T2细胞百分比显著升高(P = 0.020)。肿瘤≥5 cm的患者和低分化肿瘤患者的T1细胞百分比显著低于肿瘤<5 cm的患者以及高分化或中分化肿瘤患者(P = 0.064,P = 0.072)。有淋巴结转移和Ⅲ期至Ⅳ期肿瘤患者的T1细胞百分比显著低于无淋巴结转移和Ⅰ期至Ⅱ期肿瘤患者(P = 0.033和P = 0.033)。T1细胞数量与肿瘤大小、浆膜侵犯及远处转移等因素之间未发现显著差异。
肿瘤负荷显著抑制结直肠癌患者T1和T2细胞的分化,并可能是免疫抑制发生发展的重要因素。去除肿瘤负荷后,T1和T2细胞百分比在短时间内升高,免疫功能得到改善。检测T1可能有助于判断结直肠癌的预后。