Jennifer P. Wang, Tomoko Hayashi, Sandip K. Datta, Richard S. Kornbluth, Eyal Raz, Donald G. Guiney
{"title":"CpG寡核苷酸在人单核细胞来源的巨噬细胞中部分抑制结核分枝杆菌的生长,但不抑制沙门氏菌或李斯特菌的生长","authors":"Jennifer P. Wang, Tomoko Hayashi, Sandip K. Datta, Richard S. Kornbluth, Eyal Raz, Donald G. Guiney","doi":"10.1016/j.femsim.2005.05.007","DOIUrl":null,"url":null,"abstract":"<div><p><span><span>Immunostimulatory DNA sequences and their synthetic </span>oligonucleotide<span> analogs (CpG-ODN) activate innate immunity and can stimulate antibacterial effects against numerous intracellular pathogens. While it has been shown previously that CpG-ODN inhibit growth of </span></span><span><em>Mycobacterium avium</em></span> in murine and human macrophages, we now report that <span><em>Mycobacterium tuberculosis</em></span> growth can be inhibited by CpG-ODN treatment of human monocyte-derived macrophages (hMDM). This inhibitory effect was reversed by IFN-γ, which has been shown repeatedly to enhance the growth of virulent <em>M. tuberculosis</em> in cultured hMDM. The antibacterial effect of CpG-ODN in human macrophages was specific for <em>M. tuberculosis</em> when compared to other intracellular pathogens including <span><em>Listeria monocytogenes</em></span> and <em>Salmonella enterica</em> serovar Dublin. These data indicate that CpG-ODN can improve the ability of hMDM to contain growth of virulent <em>M. tuberculosis</em>.</p></div>","PeriodicalId":12220,"journal":{"name":"FEMS immunology and medical microbiology","volume":"45 2","pages":"Pages 303-310"},"PeriodicalIF":0.0000,"publicationDate":"2005-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.femsim.2005.05.007","citationCount":"15","resultStr":"{\"title\":\"CpG oligonucleotides partially inhibit growth of Mycobacterium tuberculosis, but not Salmonella or Listeria, in human monocyte-derived macrophages\",\"authors\":\"Jennifer P. Wang, Tomoko Hayashi, Sandip K. Datta, Richard S. Kornbluth, Eyal Raz, Donald G. Guiney\",\"doi\":\"10.1016/j.femsim.2005.05.007\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><span><span>Immunostimulatory DNA sequences and their synthetic </span>oligonucleotide<span> analogs (CpG-ODN) activate innate immunity and can stimulate antibacterial effects against numerous intracellular pathogens. While it has been shown previously that CpG-ODN inhibit growth of </span></span><span><em>Mycobacterium avium</em></span> in murine and human macrophages, we now report that <span><em>Mycobacterium tuberculosis</em></span> growth can be inhibited by CpG-ODN treatment of human monocyte-derived macrophages (hMDM). This inhibitory effect was reversed by IFN-γ, which has been shown repeatedly to enhance the growth of virulent <em>M. tuberculosis</em> in cultured hMDM. The antibacterial effect of CpG-ODN in human macrophages was specific for <em>M. tuberculosis</em> when compared to other intracellular pathogens including <span><em>Listeria monocytogenes</em></span> and <em>Salmonella enterica</em> serovar Dublin. These data indicate that CpG-ODN can improve the ability of hMDM to contain growth of virulent <em>M. tuberculosis</em>.</p></div>\",\"PeriodicalId\":12220,\"journal\":{\"name\":\"FEMS immunology and medical microbiology\",\"volume\":\"45 2\",\"pages\":\"Pages 303-310\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2005-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.femsim.2005.05.007\",\"citationCount\":\"15\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"FEMS immunology and medical microbiology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0928824405001264\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"FEMS immunology and medical microbiology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0928824405001264","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
CpG oligonucleotides partially inhibit growth of Mycobacterium tuberculosis, but not Salmonella or Listeria, in human monocyte-derived macrophages
Immunostimulatory DNA sequences and their synthetic oligonucleotide analogs (CpG-ODN) activate innate immunity and can stimulate antibacterial effects against numerous intracellular pathogens. While it has been shown previously that CpG-ODN inhibit growth of Mycobacterium avium in murine and human macrophages, we now report that Mycobacterium tuberculosis growth can be inhibited by CpG-ODN treatment of human monocyte-derived macrophages (hMDM). This inhibitory effect was reversed by IFN-γ, which has been shown repeatedly to enhance the growth of virulent M. tuberculosis in cultured hMDM. The antibacterial effect of CpG-ODN in human macrophages was specific for M. tuberculosis when compared to other intracellular pathogens including Listeria monocytogenes and Salmonella enterica serovar Dublin. These data indicate that CpG-ODN can improve the ability of hMDM to contain growth of virulent M. tuberculosis.