Macchetti Alexandre Henrique, Marana Heitor Ricardo Cosiski, Silva João Santana, de Andrade Jurandyr Moreira, Ribeiro-Silva Alfredo, Bighetti Sérgio
Department of Gynecology and Obstetrics, Breast Service, Ribeirão Preto Medical School, University of São Paulo, Brazil.
Clinics (Sao Paulo). 2006 Jun;61(3):203-8. doi: 10.1590/s1807-59322006000300004. Epub 2006 Jun 30.
The role of immune system in the pathogenesis and progression of breast cancer is a subject of controversy, and this stimulated us to investigate the association of the immunophenotype of tumor-infiltrating lymphocytes in early breast cancer with the spread of tumor cells to axillary lymph nodes.
Tumor samples from 23 patients with early breast cancer from the Department of Gynecology and Obstetrics of Ribeirão Preto Medical School (USP) were obtained at the time of biopsy and submitted to an enzyme-digestion procedure for the extraction of tumor-infiltrating lymphocytes. The lymphocytes extracted were analyzed by dual-color flow cytometry with monoclonal antibodies in these combinations: CD3 FITC/CD19 PE, CD3 FITC/CD4 PE, CD3 FITC/CD8 PE, and CD16/56 PerCP, which are specific for immunophenotyping of T and B lymphocytes, helper and cytotoxic T lymphocytes, and natural killer (NK) cells. The mean percentage of these cells was used for comparing groups of patients with or without lymph node metastasis.
The mean value for T-lymphocyte infiltration was 24.72 +/- 17.37%; for B-lymphocyte infiltration, 4.22 +/- 6.27%; for NK-cell infiltration, 4.41 +/- 5.22%, and for CD4(+) and CD8(+) T-lymphocyte infiltration, 12.43 +/- 10.12% and 11.30 +/- 15.09%, respectively. Only mean values of T- and CD4(+) T-lymphocyte infiltration were higher in the group of patients with lymph node metastasis, while no differences were noted in the other lymphocyte subpopulations.
The association of tumor-infiltrating CD4(+) T lymphocytes with lymph node metastasis suggests a role for these cells in the spread of neoplasia to lymph nodes in patients with early breast cancer.
免疫系统在乳腺癌发病机制及进展中的作用存在争议,这促使我们研究早期乳腺癌中肿瘤浸润淋巴细胞的免疫表型与肿瘤细胞向腋窝淋巴结扩散之间的关联。
从里贝朗普雷图医学院(USP)妇产科获取23例早期乳腺癌患者的肿瘤样本,在活检时采集,并进行酶消化程序以提取肿瘤浸润淋巴细胞。提取的淋巴细胞通过双色流式细胞术,使用以下单克隆抗体组合进行分析:CD3 FITC/CD19 PE、CD3 FITC/CD4 PE、CD3 FITC/CD8 PE和CD16/56 PerCP,这些抗体分别用于T和B淋巴细胞、辅助性和细胞毒性T淋巴细胞以及自然杀伤(NK)细胞的免疫表型分析。这些细胞的平均百分比用于比较有或无淋巴结转移的患者组。
T淋巴细胞浸润的平均值为24.72±17.37%;B淋巴细胞浸润为4.22±6.27%;NK细胞浸润为4.41±5.22%,CD4(+)和CD8(+) T淋巴细胞浸润分别为12.43±10.12%和11.30±15.09%。只有T淋巴细胞和CD4(+) T淋巴细胞浸润的平均值在有淋巴结转移的患者组中较高,而其他淋巴细胞亚群未观察到差异。
肿瘤浸润性CD4(+) T淋巴细胞与淋巴结转移之间的关联表明,这些细胞在早期乳腺癌患者肿瘤向淋巴结扩散中发挥作用。