{"title":"INFLUENCE OF PERITONEAL INFLAMMATORY EXUDATE ON DEVELOPMENT OF A TRANSPLANTABLE MOUSE ASCITES TUMOR.","authors":"G BARSKI, J BELEHRADEK, J KAWAMATA","doi":"10.3181/00379727-119-30111","DOIUrl":null,"url":null,"abstract":"Summary Three daily peritoneal injections of 1:1000 glycogen solution induced in mice, during at least 10 days, a state of relative resistance to intraperitoneal but not subcutaneous inoculation of homotransplantable dL-46 ascites tumor cells. Removal of excess macrophages by peritoneal washing or their transfer to untreated mice did not influence the development of dL-46 ascites. Furthermore, elaboration of specific immune reaction by intraperitoneal inoculation of irradiated cells was not enhanced in glycogen treated mice.","PeriodicalId":20675,"journal":{"name":"Proceedings of the Society for Experimental Biology and Medicine","volume":" ","pages":"111-4"},"PeriodicalIF":0.0000,"publicationDate":"1965-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3181/00379727-119-30111","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Proceedings of the Society for Experimental Biology and Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3181/00379727-119-30111","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
Summary Three daily peritoneal injections of 1:1000 glycogen solution induced in mice, during at least 10 days, a state of relative resistance to intraperitoneal but not subcutaneous inoculation of homotransplantable dL-46 ascites tumor cells. Removal of excess macrophages by peritoneal washing or their transfer to untreated mice did not influence the development of dL-46 ascites. Furthermore, elaboration of specific immune reaction by intraperitoneal inoculation of irradiated cells was not enhanced in glycogen treated mice.