{"title":"免疫刺激葡萄球菌脂磷胆酸阻止BALB/c小鼠肺肿瘤定植","authors":"Y. Ohshima, H.L. Ko, J. Beuth, G. Pulverer","doi":"10.1016/S0176-6724(88)80156-1","DOIUrl":null,"url":null,"abstract":"<div><p>Immunostimulating and antineoplastic activities of staphylococcal lipoteichoic acid (LTA) were studied in Balb/c-mice. Systemic administration of LTA (1 mg or 2 mg i.p., 7 and 4 days prior to challenge) significantly enhanced chemiluminescence response of peritoneal macrophages (p < 0.0125) and induced enlargement of the spleen (p < 0.025) as compared to non-treated controls. In vivo the number of lung colonies was significantly lower (p < 0.0125) in LTA-treated mice 14 days after challenge with L-1 sarcoma cells.</p></div>","PeriodicalId":101291,"journal":{"name":"Zentralblatt für Bakteriologie, Mikrobiologie und Hygiene. Series A: Medical Microbiology, Infectious Diseases, Virology, Parasitology","volume":"270 1","pages":"Pages 213-218"},"PeriodicalIF":0.0000,"publicationDate":"1988-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0176-6724(88)80156-1","citationCount":"9","resultStr":"{\"title\":\"Immunostimulating Staphylococcal Lipoteichoic Acid Prevents Pulmonary Tumor Colonization in BALB/c-Mice\",\"authors\":\"Y. Ohshima, H.L. Ko, J. Beuth, G. Pulverer\",\"doi\":\"10.1016/S0176-6724(88)80156-1\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Immunostimulating and antineoplastic activities of staphylococcal lipoteichoic acid (LTA) were studied in Balb/c-mice. Systemic administration of LTA (1 mg or 2 mg i.p., 7 and 4 days prior to challenge) significantly enhanced chemiluminescence response of peritoneal macrophages (p < 0.0125) and induced enlargement of the spleen (p < 0.025) as compared to non-treated controls. In vivo the number of lung colonies was significantly lower (p < 0.0125) in LTA-treated mice 14 days after challenge with L-1 sarcoma cells.</p></div>\",\"PeriodicalId\":101291,\"journal\":{\"name\":\"Zentralblatt für Bakteriologie, Mikrobiologie und Hygiene. Series A: Medical Microbiology, Infectious Diseases, Virology, Parasitology\",\"volume\":\"270 1\",\"pages\":\"Pages 213-218\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1988-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/S0176-6724(88)80156-1\",\"citationCount\":\"9\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Zentralblatt für Bakteriologie, Mikrobiologie und Hygiene. Series A: Medical Microbiology, Infectious Diseases, Virology, Parasitology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0176672488801561\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zentralblatt für Bakteriologie, Mikrobiologie und Hygiene. Series A: Medical Microbiology, Infectious Diseases, Virology, Parasitology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0176672488801561","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Immunostimulating Staphylococcal Lipoteichoic Acid Prevents Pulmonary Tumor Colonization in BALB/c-Mice
Immunostimulating and antineoplastic activities of staphylococcal lipoteichoic acid (LTA) were studied in Balb/c-mice. Systemic administration of LTA (1 mg or 2 mg i.p., 7 and 4 days prior to challenge) significantly enhanced chemiluminescence response of peritoneal macrophages (p < 0.0125) and induced enlargement of the spleen (p < 0.025) as compared to non-treated controls. In vivo the number of lung colonies was significantly lower (p < 0.0125) in LTA-treated mice 14 days after challenge with L-1 sarcoma cells.