Campylobacter jejuni Lipooligosaccharides Modulate Dendritic Cell-Mediated T Cell Polarization in a Sialic Acid Linkage-Dependent Manner
Carbohydrate mimicry between Campylobacter jejuni lipooligosaccharides (LOS) and host neural gangliosides plays a crucial role in the pathogenesis of Guillain-Barré syndrome (GBS). Campylobacter jejuni LOS may mimic various gangliosides, which affects the immunogenicity and the type of neurological...
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Veröffentlicht in: | Infection and Immunity 2011-07, Vol.79 (7), p.2681-2689 |
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creator | Bax, Marieke Kuijf, Mark L Heikema, Astrid P van Rijs, Wouter Bruijns, Sven C.M García-Vallejo, Juan J Crocker, Paul R Jacobs, Bart C van Vliet, Sandra J van Kooyk, Yvette |
description | Carbohydrate mimicry between Campylobacter jejuni lipooligosaccharides (LOS) and host neural gangliosides plays a crucial role in the pathogenesis of Guillain-Barré syndrome (GBS). Campylobacter jejuni LOS may mimic various gangliosides, which affects the immunogenicity and the type of neurological deficits in GBS patients. Previous studies have shown the interaction of LOS with sialic acid-specific siglec receptors, although the functional consequences remain unknown. Cells that express high levels of siglecs include dendritic cells (DCs), which are crucial for initiation and differentiation of immune responses. We confirm that α2,3-sialylated GD1a/GM1a mimic and α2,8-sialylated GD1c mimic LOS structures interact with recombinant Sn and siglec-7, respectively. Although the linkage of the terminal sialic acid of LOS did not regulate expression of DC maturation markers, it displayed clear opposite expression levels of interleukin-12 (IL-12) and OX40L, molecules involved in DC-mediated Th cell differentiation. Accordingly, targeting DC-expressed siglec-7 with α2,8-linked sialylated LOS resulted in Th1 responses, whereas Th2 responses were induced by targeting with LOS containing α2,3-linked sialic acid. Thus, our data demonstrate for the first time that depending on the sialylated composition of Campylobacter jejuni LOS, specific Th differentiation programs are initiated, possibly through targeting of distinct DC-expressed siglecs. |
doi_str_mv | 10.1128/IAI.00009-11 |
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Campylobacter jejuni LOS may mimic various gangliosides, which affects the immunogenicity and the type of neurological deficits in GBS patients. Previous studies have shown the interaction of LOS with sialic acid-specific siglec receptors, although the functional consequences remain unknown. Cells that express high levels of siglecs include dendritic cells (DCs), which are crucial for initiation and differentiation of immune responses. We confirm that α2,3-sialylated GD1a/GM1a mimic and α2,8-sialylated GD1c mimic LOS structures interact with recombinant Sn and siglec-7, respectively. Although the linkage of the terminal sialic acid of LOS did not regulate expression of DC maturation markers, it displayed clear opposite expression levels of interleukin-12 (IL-12) and OX40L, molecules involved in DC-mediated Th cell differentiation. Accordingly, targeting DC-expressed siglec-7 with α2,8-linked sialylated LOS resulted in Th1 responses, whereas Th2 responses were induced by targeting with LOS containing α2,3-linked sialic acid. Thus, our data demonstrate for the first time that depending on the sialylated composition of Campylobacter jejuni LOS, specific Th differentiation programs are initiated, possibly through targeting of distinct DC-expressed siglecs.</description><identifier>ISSN: 0019-9567</identifier><identifier>EISSN: 1098-5522</identifier><identifier>DOI: 10.1128/IAI.00009-11</identifier><identifier>PMID: 21502591</identifier><identifier>CODEN: INFIBR</identifier><language>eng</language><publisher>Washington, DC: American Society for Microbiology</publisher><subject>Bacteriology ; Biological and medical sciences ; Campylobacter jejuni ; Campylobacter jejuni - chemistry ; Campylobacter jejuni - immunology ; Campylobacter jejuni - metabolism ; Carbohydrate Conformation ; Cell Differentiation ; Cell Line ; Cell Polarity ; dendritic cells ; Dendritic Cells - immunology ; Dendritic Cells - metabolism ; Enzyme-Linked Immunosorbent Assay ; Flow Cytometry ; Fundamental and applied biological sciences. Psychology ; G(M1) Ganglioside - chemistry ; gangliosides ; Gangliosides - chemistry ; Gangliosides - immunology ; Gangliosides - metabolism ; Guillain-Barre Syndrome ; Guillain-Barre Syndrome - immunology ; Guillain-Barre Syndrome - microbiology ; HEK293 Cells ; Host Response and Inflammation ; Humans ; immune response ; interleukin-12 ; Interleukin-12 - biosynthesis ; Interleukin-12 - genetics ; Interleukin-12 - immunology ; Lectins - metabolism ; lipooligosaccharides ; Lipopolysaccharides - chemistry ; Lipopolysaccharides - immunology ; Lipopolysaccharides - metabolism ; Microbiology ; Miscellaneous ; Molecular Mimicry ; N-Acetylneuraminic Acid - chemistry ; N-Acetylneuraminic Acid - immunology ; N-Acetylneuraminic Acid - metabolism ; OX40 Ligand - biosynthesis ; OX40 Ligand - genetics ; pathogenesis ; patients ; Polymerase Chain Reaction ; receptors ; Sialic Acid Binding Immunoglobulin-like Lectins ; T-Lymphocytes - immunology ; T-Lymphocytes - metabolism ; Th1 Cells - immunology ; Th2 Cells - immunology</subject><ispartof>Infection and Immunity, 2011-07, Vol.79 (7), p.2681-2689</ispartof><rights>2015 INIST-CNRS</rights><rights>Copyright © 2011, American Society for Microbiology 2011 American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c463t-4901212b3f3f997815269b5226ad26267a2eb26c9f2ed0e4c661e9643a6949563</citedby><cites>FETCH-LOGICAL-c463t-4901212b3f3f997815269b5226ad26267a2eb26c9f2ed0e4c661e9643a6949563</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3191980/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3191980/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,3175,3176,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24332815$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21502591$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bax, Marieke</creatorcontrib><creatorcontrib>Kuijf, Mark L</creatorcontrib><creatorcontrib>Heikema, Astrid P</creatorcontrib><creatorcontrib>van Rijs, Wouter</creatorcontrib><creatorcontrib>Bruijns, Sven C.M</creatorcontrib><creatorcontrib>García-Vallejo, Juan J</creatorcontrib><creatorcontrib>Crocker, Paul R</creatorcontrib><creatorcontrib>Jacobs, Bart C</creatorcontrib><creatorcontrib>van Vliet, Sandra J</creatorcontrib><creatorcontrib>van Kooyk, Yvette</creatorcontrib><title>Campylobacter jejuni Lipooligosaccharides Modulate Dendritic Cell-Mediated T Cell Polarization in a Sialic Acid Linkage-Dependent Manner</title><title>Infection and Immunity</title><addtitle>Infect Immun</addtitle><description>Carbohydrate mimicry between Campylobacter jejuni lipooligosaccharides (LOS) and host neural gangliosides plays a crucial role in the pathogenesis of Guillain-Barré syndrome (GBS). Campylobacter jejuni LOS may mimic various gangliosides, which affects the immunogenicity and the type of neurological deficits in GBS patients. Previous studies have shown the interaction of LOS with sialic acid-specific siglec receptors, although the functional consequences remain unknown. Cells that express high levels of siglecs include dendritic cells (DCs), which are crucial for initiation and differentiation of immune responses. We confirm that α2,3-sialylated GD1a/GM1a mimic and α2,8-sialylated GD1c mimic LOS structures interact with recombinant Sn and siglec-7, respectively. Although the linkage of the terminal sialic acid of LOS did not regulate expression of DC maturation markers, it displayed clear opposite expression levels of interleukin-12 (IL-12) and OX40L, molecules involved in DC-mediated Th cell differentiation. Accordingly, targeting DC-expressed siglec-7 with α2,8-linked sialylated LOS resulted in Th1 responses, whereas Th2 responses were induced by targeting with LOS containing α2,3-linked sialic acid. Thus, our data demonstrate for the first time that depending on the sialylated composition of Campylobacter jejuni LOS, specific Th differentiation programs are initiated, possibly through targeting of distinct DC-expressed siglecs.</description><subject>Bacteriology</subject><subject>Biological and medical sciences</subject><subject>Campylobacter jejuni</subject><subject>Campylobacter jejuni - chemistry</subject><subject>Campylobacter jejuni - immunology</subject><subject>Campylobacter jejuni - metabolism</subject><subject>Carbohydrate Conformation</subject><subject>Cell Differentiation</subject><subject>Cell Line</subject><subject>Cell Polarity</subject><subject>dendritic cells</subject><subject>Dendritic Cells - immunology</subject><subject>Dendritic Cells - metabolism</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Flow Cytometry</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>G(M1) Ganglioside - chemistry</subject><subject>gangliosides</subject><subject>Gangliosides - chemistry</subject><subject>Gangliosides - immunology</subject><subject>Gangliosides - metabolism</subject><subject>Guillain-Barre Syndrome</subject><subject>Guillain-Barre Syndrome - immunology</subject><subject>Guillain-Barre Syndrome - microbiology</subject><subject>HEK293 Cells</subject><subject>Host Response and Inflammation</subject><subject>Humans</subject><subject>immune response</subject><subject>interleukin-12</subject><subject>Interleukin-12 - biosynthesis</subject><subject>Interleukin-12 - genetics</subject><subject>Interleukin-12 - immunology</subject><subject>Lectins - metabolism</subject><subject>lipooligosaccharides</subject><subject>Lipopolysaccharides - chemistry</subject><subject>Lipopolysaccharides - immunology</subject><subject>Lipopolysaccharides - metabolism</subject><subject>Microbiology</subject><subject>Miscellaneous</subject><subject>Molecular Mimicry</subject><subject>N-Acetylneuraminic Acid - chemistry</subject><subject>N-Acetylneuraminic Acid - immunology</subject><subject>N-Acetylneuraminic Acid - metabolism</subject><subject>OX40 Ligand - biosynthesis</subject><subject>OX40 Ligand - genetics</subject><subject>pathogenesis</subject><subject>patients</subject><subject>Polymerase Chain Reaction</subject><subject>receptors</subject><subject>Sialic Acid Binding Immunoglobulin-like Lectins</subject><subject>T-Lymphocytes - immunology</subject><subject>T-Lymphocytes - metabolism</subject><subject>Th1 Cells - immunology</subject><subject>Th2 Cells - immunology</subject><issn>0019-9567</issn><issn>1098-5522</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkk1v1DAQhiMEokvhxhnMAXEhxR-JE1-QVls-VtoVSG3P1sRxdr1k7dROQOUX8LOZdpcCvlhjP349M-9k2XNGzxjj9bvlfHlGcamcsQfZjFFV52XJ-cNsRilTuSpldZI9SWmHYVEU9ePshLOS8lKxWfZrAfvhpg8NmNFGsrO7yTuyckMIvduEBMZsIbrWJrIO7dTDaMm59W10ozNkYfs-X9vW4XFLLu9i8jX0-OInjC544jwBcuGgR3puXIvS_htsbH5uB5SxfiRr8N7Gp9mjDvpknx330-zq44fLxed89eXTcjFf5aaQYswLRRlnvBGd6JSqalZyqRosV0LLJZcVcNtwaVTHbUttYaRkVslCgFQFtkKcZu8PusPU7G1rMIMIvR6i20O80QGc_v_Gu63ehO9aMMVUTVHgzVEghuvJplHvXTJYOHgbpqTrSghWlhVD8u2BNDGkFG13_wuj-tY7jd7pO-8wRPzFv5ndw3_MQuD1EYBkoO8ieOPSX64QgmNDkHt14LZus_3hotWQ9tphZZXSleayvtV6eWA6CBo2EXWuLjgOCA5JVQsqxW-MMLa_</recordid><startdate>20110701</startdate><enddate>20110701</enddate><creator>Bax, Marieke</creator><creator>Kuijf, Mark L</creator><creator>Heikema, Astrid P</creator><creator>van Rijs, Wouter</creator><creator>Bruijns, Sven C.M</creator><creator>García-Vallejo, Juan J</creator><creator>Crocker, Paul R</creator><creator>Jacobs, Bart C</creator><creator>van Vliet, Sandra J</creator><creator>van Kooyk, Yvette</creator><general>American Society for Microbiology</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20110701</creationdate><title>Campylobacter jejuni Lipooligosaccharides Modulate Dendritic Cell-Mediated T Cell Polarization in a Sialic Acid Linkage-Dependent Manner</title><author>Bax, Marieke ; Kuijf, Mark L ; Heikema, Astrid P ; van Rijs, Wouter ; Bruijns, Sven C.M ; García-Vallejo, Juan J ; Crocker, Paul R ; Jacobs, Bart C ; van Vliet, Sandra J ; van Kooyk, Yvette</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c463t-4901212b3f3f997815269b5226ad26267a2eb26c9f2ed0e4c661e9643a6949563</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Bacteriology</topic><topic>Biological and medical sciences</topic><topic>Campylobacter jejuni</topic><topic>Campylobacter jejuni - chemistry</topic><topic>Campylobacter jejuni - immunology</topic><topic>Campylobacter jejuni - metabolism</topic><topic>Carbohydrate Conformation</topic><topic>Cell Differentiation</topic><topic>Cell Line</topic><topic>Cell Polarity</topic><topic>dendritic cells</topic><topic>Dendritic Cells - immunology</topic><topic>Dendritic Cells - metabolism</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Flow Cytometry</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>G(M1) Ganglioside - chemistry</topic><topic>gangliosides</topic><topic>Gangliosides - chemistry</topic><topic>Gangliosides - immunology</topic><topic>Gangliosides - metabolism</topic><topic>Guillain-Barre Syndrome</topic><topic>Guillain-Barre Syndrome - immunology</topic><topic>Guillain-Barre Syndrome - microbiology</topic><topic>HEK293 Cells</topic><topic>Host Response and Inflammation</topic><topic>Humans</topic><topic>immune response</topic><topic>interleukin-12</topic><topic>Interleukin-12 - biosynthesis</topic><topic>Interleukin-12 - genetics</topic><topic>Interleukin-12 - immunology</topic><topic>Lectins - metabolism</topic><topic>lipooligosaccharides</topic><topic>Lipopolysaccharides - chemistry</topic><topic>Lipopolysaccharides - immunology</topic><topic>Lipopolysaccharides - metabolism</topic><topic>Microbiology</topic><topic>Miscellaneous</topic><topic>Molecular Mimicry</topic><topic>N-Acetylneuraminic Acid - chemistry</topic><topic>N-Acetylneuraminic Acid - immunology</topic><topic>N-Acetylneuraminic Acid - metabolism</topic><topic>OX40 Ligand - biosynthesis</topic><topic>OX40 Ligand - genetics</topic><topic>pathogenesis</topic><topic>patients</topic><topic>Polymerase Chain Reaction</topic><topic>receptors</topic><topic>Sialic Acid Binding Immunoglobulin-like Lectins</topic><topic>T-Lymphocytes - immunology</topic><topic>T-Lymphocytes - metabolism</topic><topic>Th1 Cells - immunology</topic><topic>Th2 Cells - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bax, Marieke</creatorcontrib><creatorcontrib>Kuijf, Mark L</creatorcontrib><creatorcontrib>Heikema, Astrid P</creatorcontrib><creatorcontrib>van Rijs, Wouter</creatorcontrib><creatorcontrib>Bruijns, Sven C.M</creatorcontrib><creatorcontrib>García-Vallejo, Juan J</creatorcontrib><creatorcontrib>Crocker, Paul R</creatorcontrib><creatorcontrib>Jacobs, Bart C</creatorcontrib><creatorcontrib>van Vliet, Sandra J</creatorcontrib><creatorcontrib>van Kooyk, Yvette</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Infection and Immunity</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bax, Marieke</au><au>Kuijf, Mark L</au><au>Heikema, Astrid P</au><au>van Rijs, Wouter</au><au>Bruijns, Sven C.M</au><au>García-Vallejo, Juan J</au><au>Crocker, Paul R</au><au>Jacobs, Bart C</au><au>van Vliet, Sandra J</au><au>van Kooyk, Yvette</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Campylobacter jejuni Lipooligosaccharides Modulate Dendritic Cell-Mediated T Cell Polarization in a Sialic Acid Linkage-Dependent Manner</atitle><jtitle>Infection and Immunity</jtitle><addtitle>Infect Immun</addtitle><date>2011-07-01</date><risdate>2011</risdate><volume>79</volume><issue>7</issue><spage>2681</spage><epage>2689</epage><pages>2681-2689</pages><issn>0019-9567</issn><eissn>1098-5522</eissn><coden>INFIBR</coden><abstract>Carbohydrate mimicry between Campylobacter jejuni lipooligosaccharides (LOS) and host neural gangliosides plays a crucial role in the pathogenesis of Guillain-Barré syndrome (GBS). Campylobacter jejuni LOS may mimic various gangliosides, which affects the immunogenicity and the type of neurological deficits in GBS patients. Previous studies have shown the interaction of LOS with sialic acid-specific siglec receptors, although the functional consequences remain unknown. Cells that express high levels of siglecs include dendritic cells (DCs), which are crucial for initiation and differentiation of immune responses. We confirm that α2,3-sialylated GD1a/GM1a mimic and α2,8-sialylated GD1c mimic LOS structures interact with recombinant Sn and siglec-7, respectively. Although the linkage of the terminal sialic acid of LOS did not regulate expression of DC maturation markers, it displayed clear opposite expression levels of interleukin-12 (IL-12) and OX40L, molecules involved in DC-mediated Th cell differentiation. Accordingly, targeting DC-expressed siglec-7 with α2,8-linked sialylated LOS resulted in Th1 responses, whereas Th2 responses were induced by targeting with LOS containing α2,3-linked sialic acid. Thus, our data demonstrate for the first time that depending on the sialylated composition of Campylobacter jejuni LOS, specific Th differentiation programs are initiated, possibly through targeting of distinct DC-expressed siglecs.</abstract><cop>Washington, DC</cop><pub>American Society for Microbiology</pub><pmid>21502591</pmid><doi>10.1128/IAI.00009-11</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Bacteriology Biological and medical sciences Campylobacter jejuni Campylobacter jejuni - chemistry Campylobacter jejuni - immunology Campylobacter jejuni - metabolism Carbohydrate Conformation Cell Differentiation Cell Line Cell Polarity dendritic cells Dendritic Cells - immunology Dendritic Cells - metabolism Enzyme-Linked Immunosorbent Assay Flow Cytometry Fundamental and applied biological sciences. Psychology G(M1) Ganglioside - chemistry gangliosides Gangliosides - chemistry Gangliosides - immunology Gangliosides - metabolism Guillain-Barre Syndrome Guillain-Barre Syndrome - immunology Guillain-Barre Syndrome - microbiology HEK293 Cells Host Response and Inflammation Humans immune response interleukin-12 Interleukin-12 - biosynthesis Interleukin-12 - genetics Interleukin-12 - immunology Lectins - metabolism lipooligosaccharides Lipopolysaccharides - chemistry Lipopolysaccharides - immunology Lipopolysaccharides - metabolism Microbiology Miscellaneous Molecular Mimicry N-Acetylneuraminic Acid - chemistry N-Acetylneuraminic Acid - immunology N-Acetylneuraminic Acid - metabolism OX40 Ligand - biosynthesis OX40 Ligand - genetics pathogenesis patients Polymerase Chain Reaction receptors Sialic Acid Binding Immunoglobulin-like Lectins T-Lymphocytes - immunology T-Lymphocytes - metabolism Th1 Cells - immunology Th2 Cells - immunology |
title | Campylobacter jejuni Lipooligosaccharides Modulate Dendritic Cell-Mediated T Cell Polarization in a Sialic Acid Linkage-Dependent Manner |
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