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Different Transcriptional Profiles of Human Monocyte-Derived Dendritic Cells Infected with Distinct Strains of Mycobacterium tuberculosis and Mycobacterium bovis Bacillus Calmette-Guérin
In order to analyze dendritic cells (DCs) activation following infection with different mycobacterial strains, we studied the expression profiles of 165 genes of human monocyte-derived DCs infected with H37Rv, a virulent Mycobacterium tuberculosis (MTB) laboratory strain, CMT97, a clinical MTB isola...
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Published in: | Clinical & developmental immunology 2011-01, Vol.2011 (2011), p.1-14 |
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description | In order to analyze dendritic cells (DCs) activation following infection with different mycobacterial strains, we studied the expression profiles of 165 genes of human monocyte-derived DCs infected with H37Rv, a virulent Mycobacterium tuberculosis (MTB) laboratory strain, CMT97, a clinical MTB isolate, Mycobacterium bovis bacillus Calmette-Guérin (BCG), Aventis Pasteur, and BCG Japan, both employed as vaccine against tuberculosis. The analysis of the gene expression reveals that, despite a set of genes similarly modulated, DCs response resulted strain dependent. In particular, H37Rv significantly upregulated EBI3 expression compared with BCG Japan, while it was the only strain that failed to release a significant IL-10 amount. Of note, BCG Japan showed a marked increase in CCR7 and TNF-α expression regarding both MTB strains and it resulted the only strain failing in exponential intracellular growth. Our results suggest that DCs display the ability to elicit a tailored strain-specific immune response. |
doi_str_mv | 10.1155/2011/741051 |
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The analysis of the gene expression reveals that, despite a set of genes similarly modulated, DCs response resulted strain dependent. In particular, H37Rv significantly upregulated EBI3 expression compared with BCG Japan, while it was the only strain that failed to release a significant IL-10 amount. Of note, BCG Japan showed a marked increase in CCR7 and TNF-α expression regarding both MTB strains and it resulted the only strain failing in exponential intracellular growth. Our results suggest that DCs display the ability to elicit a tailored strain-specific immune response.</description><identifier>ISSN: 1740-2522</identifier><identifier>ISSN: 2314-8861</identifier><identifier>EISSN: 1740-2530</identifier><identifier>EISSN: 2314-7156</identifier><identifier>DOI: 10.1155/2011/741051</identifier><identifier>PMID: 21436989</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Puplishing Corporation</publisher><subject>Bacteria ; Dendritic Cells - immunology ; Dendritic Cells - metabolism ; Dendritic Cells - microbiology ; Dendritic Cells - pathology ; Gene expression ; Gene Expression Profiling ; Humans ; Immune system ; Immunology ; Immunophenotyping ; Interleukin-10 - genetics ; Interleukin-10 - metabolism ; Interleukins - genetics ; Interleukins - metabolism ; Minor Histocompatibility Antigens ; Monocytes - pathology ; Mycobacterium bovis ; Mycobacterium bovis - immunology ; Mycobacterium bovis - pathogenicity ; Mycobacterium tuberculosis ; Mycobacterium tuberculosis - immunology ; Mycobacterium tuberculosis - pathogenicity ; Neurosciences ; Receptors, CCR7 - genetics ; Receptors, CCR7 - metabolism ; Species Specificity ; Studies ; Tuberculosis - immunology ; Tuberculosis - microbiology ; Tuberculosis - prevention & control ; Tuberculosis Vaccines ; Tumor Necrosis Factor-alpha - genetics ; Tumor Necrosis Factor-alpha - metabolism ; Virulence</subject><ispartof>Clinical & developmental immunology, 2011-01, Vol.2011 (2011), p.1-14</ispartof><rights>Copyright © 2011 Nunzia Sanarico et al.</rights><rights>Copyright © 2011 Nunzia Sanarico et al. Nunzia Sanarico et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>Copyright © 2011 Nunzia Sanarico et al. 2011</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c525t-dc720fc698d672a97e97c7f3625ca09ea50628b9f2cbc5613d3fceef84ba365f3</citedby><cites>FETCH-LOGICAL-c525t-dc720fc698d672a97e97c7f3625ca09ea50628b9f2cbc5613d3fceef84ba365f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/879093439/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/879093439?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21436989$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Winter, Nathalie</contributor><creatorcontrib>Sanarico, Nunzia</creatorcontrib><creatorcontrib>Colone, Alessia</creatorcontrib><creatorcontrib>Grassi, Manuela</creatorcontrib><creatorcontrib>Speranza, Viviana</creatorcontrib><creatorcontrib>Giovannini, Daniela</creatorcontrib><creatorcontrib>Ciaramella, Antonio</creatorcontrib><creatorcontrib>Colizzi, Vittorio</creatorcontrib><creatorcontrib>Mariani, Francesca</creatorcontrib><title>Different Transcriptional Profiles of Human Monocyte-Derived Dendritic Cells Infected with Distinct Strains of Mycobacterium tuberculosis and Mycobacterium bovis Bacillus Calmette-Guérin</title><title>Clinical & developmental immunology</title><addtitle>Clin Dev Immunol</addtitle><description>In order to analyze dendritic cells (DCs) activation following infection with different mycobacterial strains, we studied the expression profiles of 165 genes of human monocyte-derived DCs infected with H37Rv, a virulent Mycobacterium tuberculosis (MTB) laboratory strain, CMT97, a clinical MTB isolate, Mycobacterium bovis bacillus Calmette-Guérin (BCG), Aventis Pasteur, and BCG Japan, both employed as vaccine against tuberculosis. 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The analysis of the gene expression reveals that, despite a set of genes similarly modulated, DCs response resulted strain dependent. In particular, H37Rv significantly upregulated EBI3 expression compared with BCG Japan, while it was the only strain that failed to release a significant IL-10 amount. Of note, BCG Japan showed a marked increase in CCR7 and TNF-α expression regarding both MTB strains and it resulted the only strain failing in exponential intracellular growth. Our results suggest that DCs display the ability to elicit a tailored strain-specific immune response.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Puplishing Corporation</pub><pmid>21436989</pmid><doi>10.1155/2011/741051</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Bacteria Dendritic Cells - immunology Dendritic Cells - metabolism Dendritic Cells - microbiology Dendritic Cells - pathology Gene expression Gene Expression Profiling Humans Immune system Immunology Immunophenotyping Interleukin-10 - genetics Interleukin-10 - metabolism Interleukins - genetics Interleukins - metabolism Minor Histocompatibility Antigens Monocytes - pathology Mycobacterium bovis Mycobacterium bovis - immunology Mycobacterium bovis - pathogenicity Mycobacterium tuberculosis Mycobacterium tuberculosis - immunology Mycobacterium tuberculosis - pathogenicity Neurosciences Receptors, CCR7 - genetics Receptors, CCR7 - metabolism Species Specificity Studies Tuberculosis - immunology Tuberculosis - microbiology Tuberculosis - prevention & control Tuberculosis Vaccines Tumor Necrosis Factor-alpha - genetics Tumor Necrosis Factor-alpha - metabolism Virulence |
title | Different Transcriptional Profiles of Human Monocyte-Derived Dendritic Cells Infected with Distinct Strains of Mycobacterium tuberculosis and Mycobacterium bovis Bacillus Calmette-Guérin |
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