{"title":"胃癌树突状细胞、巨噬细胞和淋巴细胞的免疫组化研究。","authors":"H. Iwase, K. Morise","doi":"10.3960/JSLRT1961.32.235","DOIUrl":null,"url":null,"abstract":"Infiltration of dendritic cells, macrophages and lymphcytes into tumor tissues was immunohistochemically investigated using new monoclonal antibodies ID-1 for dendritic cells and CD68 for macrophages in 68 patients with gastric cancer. A serial section technique and double staining method were used for the phenotypic analysis. In the normal musosa, ID-1+ cells were located under the surface epithelium, while CD68+ cells were widely distributed in the lamina propria. Most of ID-1+ cells and CD68+ cells in the normal mucosa were negative for ICAM-1 and activated markers of CD25 and HLA-DR antigens. In cases of mucosal cancer, the numbers of ID-1+ cells and CD 68+ cells in the cancer tissue were similar to the normal mucosa. When cancer cells invaded the submucosa, ID-1+ cells and CD68+ cells were significantly increased in the cancer tissue except for the cases of signet ring cell carcinoma. The increased ID-1+ cells were positive for ICAM-1, HLA-DR, CD25 and CD11c, while most of CD68+ cells were negative for ICAM-1 and CD25 antigans. Further, ID-1+ cells were predominantly distributed adjacent to the tumor tissues with a marked infiltration of CD3+ cells. Conversely, CD68+ cells were distributed in the cancer stroma and necrotic tissues without CD3+ cell infiltration. These findings suggested that ID-1+ dendritic cells play a crucial role in the immune response agaist the cancer tissue.","PeriodicalId":237003,"journal":{"name":"Journal of the Japan Society of the Reticuloendothelial System","volume":"90 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Immunohistochemical study of dendritic cells, macrophages and lymphocytes in gastric cancer.\",\"authors\":\"H. Iwase, K. Morise\",\"doi\":\"10.3960/JSLRT1961.32.235\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Infiltration of dendritic cells, macrophages and lymphcytes into tumor tissues was immunohistochemically investigated using new monoclonal antibodies ID-1 for dendritic cells and CD68 for macrophages in 68 patients with gastric cancer. A serial section technique and double staining method were used for the phenotypic analysis. In the normal musosa, ID-1+ cells were located under the surface epithelium, while CD68+ cells were widely distributed in the lamina propria. Most of ID-1+ cells and CD68+ cells in the normal mucosa were negative for ICAM-1 and activated markers of CD25 and HLA-DR antigens. In cases of mucosal cancer, the numbers of ID-1+ cells and CD 68+ cells in the cancer tissue were similar to the normal mucosa. When cancer cells invaded the submucosa, ID-1+ cells and CD68+ cells were significantly increased in the cancer tissue except for the cases of signet ring cell carcinoma. The increased ID-1+ cells were positive for ICAM-1, HLA-DR, CD25 and CD11c, while most of CD68+ cells were negative for ICAM-1 and CD25 antigans. Further, ID-1+ cells were predominantly distributed adjacent to the tumor tissues with a marked infiltration of CD3+ cells. Conversely, CD68+ cells were distributed in the cancer stroma and necrotic tissues without CD3+ cell infiltration. These findings suggested that ID-1+ dendritic cells play a crucial role in the immune response agaist the cancer tissue.\",\"PeriodicalId\":237003,\"journal\":{\"name\":\"Journal of the Japan Society of the Reticuloendothelial System\",\"volume\":\"90 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1900-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of the Japan Society of the Reticuloendothelial System\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3960/JSLRT1961.32.235\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the Japan Society of the Reticuloendothelial System","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3960/JSLRT1961.32.235","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Immunohistochemical study of dendritic cells, macrophages and lymphocytes in gastric cancer.
Infiltration of dendritic cells, macrophages and lymphcytes into tumor tissues was immunohistochemically investigated using new monoclonal antibodies ID-1 for dendritic cells and CD68 for macrophages in 68 patients with gastric cancer. A serial section technique and double staining method were used for the phenotypic analysis. In the normal musosa, ID-1+ cells were located under the surface epithelium, while CD68+ cells were widely distributed in the lamina propria. Most of ID-1+ cells and CD68+ cells in the normal mucosa were negative for ICAM-1 and activated markers of CD25 and HLA-DR antigens. In cases of mucosal cancer, the numbers of ID-1+ cells and CD 68+ cells in the cancer tissue were similar to the normal mucosa. When cancer cells invaded the submucosa, ID-1+ cells and CD68+ cells were significantly increased in the cancer tissue except for the cases of signet ring cell carcinoma. The increased ID-1+ cells were positive for ICAM-1, HLA-DR, CD25 and CD11c, while most of CD68+ cells were negative for ICAM-1 and CD25 antigans. Further, ID-1+ cells were predominantly distributed adjacent to the tumor tissues with a marked infiltration of CD3+ cells. Conversely, CD68+ cells were distributed in the cancer stroma and necrotic tissues without CD3+ cell infiltration. These findings suggested that ID-1+ dendritic cells play a crucial role in the immune response agaist the cancer tissue.