Ohtani H, Naito Y, Saito K, Nagura H
Department of Pathology, Tohoku University School of Medicine, Sendai, Japan.
Lab Invest. 1997 Sep;77(3):231-41.
Costimulatory molecules B7-1 (CD80) and B7-2 (CD86) are indispensable for T-cell activation. Recently, a paucity of these costimulatory molecules was reported in inflammatory cells in colon cancer, which may permit the immune evasion of the cancer. The present study uses immunohistochemistry to reveal the expression of these molecules in 43 cases of colorectal cancer tissue. B7-2 was expressed in mononuclear calls distributed along the invasive margin in 37 of 43 cases. B7-1 was positive in the same area in 22 cases. In contrast, the expression of B7-1/B7-2 was usually inconspicuous in the stroma within cancer. Most B7-1+ and B7-2+ cells were identified as macrophages because of the coexpression of CD68 antigen or acid phosphatase activity. CD4+ or CD8+ T cells were distributed in the same area and were in close contact to B7-1/B7-2+ cells. Both CD4+ and CD8+ T cells had a proliferative activity with a labeling index of Ki-67 of 1.5% and 2.5%, respectively. Conventional electron microscopy confirmed both the accumulation of macrophages along the invasive margin and the attachment of lymphocytes to them. Immunoelectron microscopy confirmed: (a) localization of B7-2/B7-1 along the cell membrane; (b) abundance of vacuoles and heterophagosomes (a finding indicative of phagocytosis of other cells) in the cytoplasm of these cells; and (c) direct cell-to-cell contact between these macrophages and lymphocytes. The present data, which suggest that an immune reaction occurs along the invasive margin of colorectal cancer, are in accordance with previous clinicopathologic studies suggesting that peritumoral lymphocytic infiltration is one of the favorable prognostic factors in this disease.
共刺激分子B7-1(CD80)和B7-2(CD86)对于T细胞活化不可或缺。最近,有报道称在结肠癌的炎症细胞中这些共刺激分子数量不足,这可能使癌症实现免疫逃逸。本研究采用免疫组织化学方法揭示这些分子在43例结直肠癌组织中的表达情况。在43例中的37例中,B7-2在沿浸润边缘分布的单核细胞中表达。22例在同一区域B7-1呈阳性。相比之下,癌内基质中B7-1/B7-2的表达通常不明显。由于CD68抗原共表达或酸性磷酸酶活性,大多数B7-1+和B7-2+细胞被鉴定为巨噬细胞。CD4+或CD8+ T细胞分布在同一区域,并与B7-1/B7-2+细胞紧密接触。CD4+和CD8+ T细胞均具有增殖活性,Ki-67标记指数分别为1.5%和2.5%。传统电子显微镜证实巨噬细胞沿浸润边缘聚集以及淋巴细胞与它们的附着情况。免疫电子显微镜证实:(a)B7-2/B7-1定位于细胞膜;(b)这些细胞的细胞质中有丰富的液泡和异噬体(这一发现表明吞噬了其他细胞);(c)这些巨噬细胞与淋巴细胞之间存在直接的细胞间接触。本研究数据表明结直肠癌浸润边缘发生免疫反应,这与之前的临床病理研究结果一致,即肿瘤周围淋巴细胞浸润是该疾病良好的预后因素之一。