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Immunotherapy with CpG DNA conjugated with T-cell epitope peptide of an allergenic Cry j 2 protein is useful for control of allergic conditions in mice
Immunotherapy using T-cell epitope peptides or CpG DNA conjugated with allergenic protein is useful, although the mechanisms of these therapies differ. However, the combination of CpG DNA and peptide, but not protein, had not been documented. Therefore, we investigated CpG DNA conjugated with peptid...
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Published in: | International immunopharmacology 2007-01, Vol.7 (1), p.46-54 |
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description | Immunotherapy using T-cell epitope peptides or CpG DNA conjugated with allergenic protein is useful, although the mechanisms of these therapies differ. However, the combination of CpG DNA and peptide, but not protein, had not been documented. Therefore, we investigated CpG DNA conjugated with peptide to obtain positive synergistic effects. In the first experiment, mice were vaccinated with a conjugate of CpG DNA and Cry j 2 T-cell epitope peptide p246-259 (CpG-peptide); a mixture of CpG DNA and peptide (CpG+peptide); peptide alone, or PBS alone, and immunized with Cry j 2. In the second experiment, mice were immunized with Cry j 2 and injected with CpG-peptide, CpG+peptide, peptide only, or PBS only. In both experiments, Cry j 2-specific IgE, IL-4, and IL-5 were significantly lower in mice given CpG-peptide, versus those given CpG+peptide, peptide alone, or PBS alone. However, IgG2a, IgG2b and IFN-γ did not increase in mice injected with CpG-peptide. In the third experiment, CpG-peptide significantly attenuated nasal symptoms (sneezing and nasal rubbing) compared to CpG+peptide, peptide alone, or PBS alone. Mice were also injected with a conjugate of CpG DNA and Cry j 2 protein (CpG-Cry j 2) or CpG-peptide to compare prime responses. Mice vaccinated with CpG-Cry j 2 generated Cry j 2-specific IgG1, whereas those vaccinated with CpG-peptide did not produce IgG1. This study demonstrated, for the first time, that immunotherapy with CpG DNA conjugated with a T-cell peptide is useful in preventing and treating allergic conditions. |
doi_str_mv | 10.1016/j.intimp.2006.08.010 |
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However, the combination of CpG DNA and peptide, but not protein, had not been documented. Therefore, we investigated CpG DNA conjugated with peptide to obtain positive synergistic effects. In the first experiment, mice were vaccinated with a conjugate of CpG DNA and Cry j 2 T-cell epitope peptide p246-259 (CpG-peptide); a mixture of CpG DNA and peptide (CpG+peptide); peptide alone, or PBS alone, and immunized with Cry j 2. In the second experiment, mice were immunized with Cry j 2 and injected with CpG-peptide, CpG+peptide, peptide only, or PBS only. In both experiments, Cry j 2-specific IgE, IL-4, and IL-5 were significantly lower in mice given CpG-peptide, versus those given CpG+peptide, peptide alone, or PBS alone. However, IgG2a, IgG2b and IFN-γ did not increase in mice injected with CpG-peptide. In the third experiment, CpG-peptide significantly attenuated nasal symptoms (sneezing and nasal rubbing) compared to CpG+peptide, peptide alone, or PBS alone. Mice were also injected with a conjugate of CpG DNA and Cry j 2 protein (CpG-Cry j 2) or CpG-peptide to compare prime responses. Mice vaccinated with CpG-Cry j 2 generated Cry j 2-specific IgG1, whereas those vaccinated with CpG-peptide did not produce IgG1. This study demonstrated, for the first time, that immunotherapy with CpG DNA conjugated with a T-cell peptide is useful in preventing and treating allergic conditions.</description><identifier>ISSN: 1567-5769</identifier><identifier>EISSN: 1878-1705</identifier><identifier>DOI: 10.1016/j.intimp.2006.08.010</identifier><identifier>PMID: 17161816</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Allergy ; Animals ; Biological and medical sciences ; CpG DNA ; CpG Islands ; DNA - chemistry ; DNA - therapeutic use ; Epitopes, T-Lymphocyte - chemistry ; Epitopes, T-Lymphocyte - therapeutic use ; Immunoglobulin E - blood ; Immunotherapy ; Interleukin-4 - immunology ; Interleukin-5 - immunology ; Japanese cedar ; Medical sciences ; Mice ; Mice, Inbred BALB C ; Peptide therapy ; Peptides - chemistry ; Peptides - therapeutic use ; Pharmacology. Drug treatments ; Plant Proteins - chemistry ; Plant Proteins - therapeutic use ; Rhinitis, Allergic, Seasonal - therapy ; Sneezing ; Spleen - cytology ; Spleen - immunology</subject><ispartof>International immunopharmacology, 2007-01, Vol.7 (1), p.46-54</ispartof><rights>2006 Elsevier B.V.</rights><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c421t-f6ad86c9dfa2b3e018176b81592b9f63747acf6052fd95a4f2e4db33b8fbbb443</citedby><cites>FETCH-LOGICAL-c421t-f6ad86c9dfa2b3e018176b81592b9f63747acf6052fd95a4f2e4db33b8fbbb443</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18403224$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17161816$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Suzuki, Motohiko</creatorcontrib><creatorcontrib>Ohta, Nobuo</creatorcontrib><creatorcontrib>Min, Wei-Ping</creatorcontrib><creatorcontrib>Matsumoto, Tamami</creatorcontrib><creatorcontrib>Min, Rui</creatorcontrib><creatorcontrib>Zhang, Xusheng</creatorcontrib><creatorcontrib>Toida, Kazunori</creatorcontrib><creatorcontrib>Murakami, Shingo</creatorcontrib><title>Immunotherapy with CpG DNA conjugated with T-cell epitope peptide of an allergenic Cry j 2 protein is useful for control of allergic conditions in mice</title><title>International immunopharmacology</title><addtitle>Int Immunopharmacol</addtitle><description>Immunotherapy using T-cell epitope peptides or CpG DNA conjugated with allergenic protein is useful, although the mechanisms of these therapies differ. However, the combination of CpG DNA and peptide, but not protein, had not been documented. Therefore, we investigated CpG DNA conjugated with peptide to obtain positive synergistic effects. In the first experiment, mice were vaccinated with a conjugate of CpG DNA and Cry j 2 T-cell epitope peptide p246-259 (CpG-peptide); a mixture of CpG DNA and peptide (CpG+peptide); peptide alone, or PBS alone, and immunized with Cry j 2. In the second experiment, mice were immunized with Cry j 2 and injected with CpG-peptide, CpG+peptide, peptide only, or PBS only. In both experiments, Cry j 2-specific IgE, IL-4, and IL-5 were significantly lower in mice given CpG-peptide, versus those given CpG+peptide, peptide alone, or PBS alone. However, IgG2a, IgG2b and IFN-γ did not increase in mice injected with CpG-peptide. In the third experiment, CpG-peptide significantly attenuated nasal symptoms (sneezing and nasal rubbing) compared to CpG+peptide, peptide alone, or PBS alone. Mice were also injected with a conjugate of CpG DNA and Cry j 2 protein (CpG-Cry j 2) or CpG-peptide to compare prime responses. Mice vaccinated with CpG-Cry j 2 generated Cry j 2-specific IgG1, whereas those vaccinated with CpG-peptide did not produce IgG1. This study demonstrated, for the first time, that immunotherapy with CpG DNA conjugated with a T-cell peptide is useful in preventing and treating allergic conditions.</description><subject>Allergy</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>CpG DNA</subject><subject>CpG Islands</subject><subject>DNA - chemistry</subject><subject>DNA - therapeutic use</subject><subject>Epitopes, T-Lymphocyte - chemistry</subject><subject>Epitopes, T-Lymphocyte - therapeutic use</subject><subject>Immunoglobulin E - blood</subject><subject>Immunotherapy</subject><subject>Interleukin-4 - immunology</subject><subject>Interleukin-5 - immunology</subject><subject>Japanese cedar</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Peptide therapy</subject><subject>Peptides - chemistry</subject><subject>Peptides - therapeutic use</subject><subject>Pharmacology. Drug treatments</subject><subject>Plant Proteins - chemistry</subject><subject>Plant Proteins - therapeutic use</subject><subject>Rhinitis, Allergic, Seasonal - therapy</subject><subject>Sneezing</subject><subject>Spleen - cytology</subject><subject>Spleen - immunology</subject><issn>1567-5769</issn><issn>1878-1705</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNqFkcFu1TAQRSMEoqXwBwh5A7sE20kcZ4NUPaBUqmBT1pZjj1tHiR1sp-h9Cb-L0zypO1jZGp17NXduUbwluCKYsI9jZV2y81JRjFmFeYUJflacE97xknS4fZ7_LevKtmP9WfEqxhHjPG_Iy-KMdIQRTth58ed6nlfn0z0EuRzRb5vu0WG5Qp-_XyLl3bjeyQR6n9-WCqYJwWKTXwAtsCSrAXmDpENymiDcgbMKHcIRjYiiJfgE1iEb0RrBrBMyPmyuKfjpUfaoyYo80zZZ7yLK_GwVvC5eGDlFeHN6L4qfX7_cHr6VNz-urg-XN6VqKEmlYVJzpnptJB1qwDlUxwZO2p4OvWF113RSGYZbanTfysZQaPRQ1wM3wzA0TX1RfNh987K_VohJzDZuMaUDv0bBeM1Yi-l_QYpZnY_KMtjsoAo-xgBGLMHOMhwFwWJrToxib05szQnMRW4uy96d_NdhBv0kOlWVgfcnQEYlJxOkUzY-cbzBNaVbok87B_lsDxaCiMqCU6BtAJWE9vbfm_wFeCi6uw</recordid><startdate>200701</startdate><enddate>200701</enddate><creator>Suzuki, Motohiko</creator><creator>Ohta, Nobuo</creator><creator>Min, Wei-Ping</creator><creator>Matsumoto, Tamami</creator><creator>Min, Rui</creator><creator>Zhang, Xusheng</creator><creator>Toida, Kazunori</creator><creator>Murakami, Shingo</creator><general>Elsevier B.V</general><general>Elsevier</general><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>7QO</scope><scope>7T5</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>200701</creationdate><title>Immunotherapy with CpG DNA conjugated with T-cell epitope peptide of an allergenic Cry j 2 protein is useful for control of allergic conditions in mice</title><author>Suzuki, Motohiko ; Ohta, Nobuo ; Min, Wei-Ping ; Matsumoto, Tamami ; Min, Rui ; Zhang, Xusheng ; Toida, Kazunori ; Murakami, Shingo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c421t-f6ad86c9dfa2b3e018176b81592b9f63747acf6052fd95a4f2e4db33b8fbbb443</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Allergy</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>CpG DNA</topic><topic>CpG Islands</topic><topic>DNA - chemistry</topic><topic>DNA - therapeutic use</topic><topic>Epitopes, T-Lymphocyte - chemistry</topic><topic>Epitopes, T-Lymphocyte - therapeutic use</topic><topic>Immunoglobulin E - blood</topic><topic>Immunotherapy</topic><topic>Interleukin-4 - immunology</topic><topic>Interleukin-5 - immunology</topic><topic>Japanese cedar</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Peptide therapy</topic><topic>Peptides - chemistry</topic><topic>Peptides - therapeutic use</topic><topic>Pharmacology. Drug treatments</topic><topic>Plant Proteins - chemistry</topic><topic>Plant Proteins - therapeutic use</topic><topic>Rhinitis, Allergic, Seasonal - therapy</topic><topic>Sneezing</topic><topic>Spleen - cytology</topic><topic>Spleen - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Suzuki, Motohiko</creatorcontrib><creatorcontrib>Ohta, Nobuo</creatorcontrib><creatorcontrib>Min, Wei-Ping</creatorcontrib><creatorcontrib>Matsumoto, Tamami</creatorcontrib><creatorcontrib>Min, Rui</creatorcontrib><creatorcontrib>Zhang, Xusheng</creatorcontrib><creatorcontrib>Toida, Kazunori</creatorcontrib><creatorcontrib>Murakami, Shingo</creatorcontrib><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>Biotechnology Research Abstracts</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>International immunopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Suzuki, Motohiko</au><au>Ohta, Nobuo</au><au>Min, Wei-Ping</au><au>Matsumoto, Tamami</au><au>Min, Rui</au><au>Zhang, Xusheng</au><au>Toida, Kazunori</au><au>Murakami, Shingo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immunotherapy with CpG DNA conjugated with T-cell epitope peptide of an allergenic Cry j 2 protein is useful for control of allergic conditions in mice</atitle><jtitle>International immunopharmacology</jtitle><addtitle>Int Immunopharmacol</addtitle><date>2007-01</date><risdate>2007</risdate><volume>7</volume><issue>1</issue><spage>46</spage><epage>54</epage><pages>46-54</pages><issn>1567-5769</issn><eissn>1878-1705</eissn><abstract>Immunotherapy using T-cell epitope peptides or CpG DNA conjugated with allergenic protein is useful, although the mechanisms of these therapies differ. However, the combination of CpG DNA and peptide, but not protein, had not been documented. Therefore, we investigated CpG DNA conjugated with peptide to obtain positive synergistic effects. In the first experiment, mice were vaccinated with a conjugate of CpG DNA and Cry j 2 T-cell epitope peptide p246-259 (CpG-peptide); a mixture of CpG DNA and peptide (CpG+peptide); peptide alone, or PBS alone, and immunized with Cry j 2. In the second experiment, mice were immunized with Cry j 2 and injected with CpG-peptide, CpG+peptide, peptide only, or PBS only. In both experiments, Cry j 2-specific IgE, IL-4, and IL-5 were significantly lower in mice given CpG-peptide, versus those given CpG+peptide, peptide alone, or PBS alone. However, IgG2a, IgG2b and IFN-γ did not increase in mice injected with CpG-peptide. In the third experiment, CpG-peptide significantly attenuated nasal symptoms (sneezing and nasal rubbing) compared to CpG+peptide, peptide alone, or PBS alone. Mice were also injected with a conjugate of CpG DNA and Cry j 2 protein (CpG-Cry j 2) or CpG-peptide to compare prime responses. Mice vaccinated with CpG-Cry j 2 generated Cry j 2-specific IgG1, whereas those vaccinated with CpG-peptide did not produce IgG1. This study demonstrated, for the first time, that immunotherapy with CpG DNA conjugated with a T-cell peptide is useful in preventing and treating allergic conditions.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>17161816</pmid><doi>10.1016/j.intimp.2006.08.010</doi><tpages>9</tpages></addata></record> |
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subjects | Allergy Animals Biological and medical sciences CpG DNA CpG Islands DNA - chemistry DNA - therapeutic use Epitopes, T-Lymphocyte - chemistry Epitopes, T-Lymphocyte - therapeutic use Immunoglobulin E - blood Immunotherapy Interleukin-4 - immunology Interleukin-5 - immunology Japanese cedar Medical sciences Mice Mice, Inbred BALB C Peptide therapy Peptides - chemistry Peptides - therapeutic use Pharmacology. Drug treatments Plant Proteins - chemistry Plant Proteins - therapeutic use Rhinitis, Allergic, Seasonal - therapy Sneezing Spleen - cytology Spleen - immunology |
title | Immunotherapy with CpG DNA conjugated with T-cell epitope peptide of an allergenic Cry j 2 protein is useful for control of allergic conditions in mice |
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