BREAKTHROUGH OF IMMUNE SELF-TOLERANCE TO CALRETICULIN INDUCED BY CpG-OLIGODEOXYNUCLEOTIDES AS ADJUVANT
Reportedly, bacterial DNA containing unmethylated cytosine-guanosine dinucleotide motif-containing oligodeoxynucleotides (CpG-ODNs) can induce Th1-type adjuvant effects. We produced autoantibodies and induced hepatitis in mice using extracted proteins from human hepatocytes with CpG-ODNs as adjuvant...
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creator | ABE, KAZUMICHI OHIRA, HIROMASA KOBAYASHI, HIROKO SAITO, HIRONOBU TAKAHASHI, ATSUSHI RAI, TSUYOSHI KANNO, YUKIKO MONOE, KYOKO WATANABE, HIROSHI IRISAWA, ATSUSHI SATO, YUKIO |
description | Reportedly, bacterial DNA containing unmethylated cytosine-guanosine dinucleotide motif-containing oligodeoxynucleotides (CpG-ODNs) can induce Th1-type adjuvant effects. We produced autoantibodies and induced hepatitis in mice using extracted proteins from human hepatocytes with CpG-ODNs as adjuvant. Western blot analysis was performed of sera from immunized mice and two patients with autoimmune hepatitis (AIH). When a common band was detected, N-terminal amino acid sequencing was performed to determine its site. For detection of antibodies against the identified protein (calreticulin), ELISA was performed of sera of 50 patients with AIH: 45 with primary biliary cirrhosis (PBC), 24 with chronic hepatitis C (CH), and 24 healthy controls. Mice were immunized with calreticulin protein with CpG-ODNs as adjuvant. Several reacted bands were detected in their sera; in addition, a common band to the sera of patients with AIH was detected at 60 kDa. Subsequent N-terminal amino acid sequencing revealed that the protein was human calreticulin. ELISA showed that, of patients with AIH, PBC, and CH, 30.0% (15/50), 17.8% (8/45), and 12.5% (3/24), respectively, were positive for anti-calreticulin antibodies. Splenocytes from immunized mice produced IFN-γ after they were pulsed with calreticulin protein. Histological analyses of liver specimens taken from mice immunized with calreticulin protein together with CpG-ODN s showed spotty and focal necrosis. Immunofluorescence analysis showed increased expression of calreticulin in the liver treated with CpG-ODNs. These results suggest that a breakthrough of immune self-tolerance to calreticulin is induced with CpG-ODNs as adjuvant and that calreticulin protein might be a target antigen in this model. |
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We produced autoantibodies and induced hepatitis in mice using extracted proteins from human hepatocytes with CpG-ODNs as adjuvant. Western blot analysis was performed of sera from immunized mice and two patients with autoimmune hepatitis (AIH). When a common band was detected, N-terminal amino acid sequencing was performed to determine its site. For detection of antibodies against the identified protein (calreticulin), ELISA was performed of sera of 50 patients with AIH: 45 with primary biliary cirrhosis (PBC), 24 with chronic hepatitis C (CH), and 24 healthy controls. Mice were immunized with calreticulin protein with CpG-ODNs as adjuvant. Several reacted bands were detected in their sera; in addition, a common band to the sera of patients with AIH was detected at 60 kDa. Subsequent N-terminal amino acid sequencing revealed that the protein was human calreticulin. ELISA showed that, of patients with AIH, PBC, and CH, 30.0% (15/50), 17.8% (8/45), and 12.5% (3/24), respectively, were positive for anti-calreticulin antibodies. Splenocytes from immunized mice produced IFN-γ after they were pulsed with calreticulin protein. Histological analyses of liver specimens taken from mice immunized with calreticulin protein together with CpG-ODN s showed spotty and focal necrosis. Immunofluorescence analysis showed increased expression of calreticulin in the liver treated with CpG-ODNs. These results suggest that a breakthrough of immune self-tolerance to calreticulin is induced with CpG-ODNs as adjuvant and that calreticulin protein might be a target antigen in this model.</description><identifier>ISSN: 0016-2590</identifier><identifier>EISSN: 2185-4610</identifier><identifier>DOI: 10.5387/fms.53.95</identifier><identifier>PMID: 18402289</identifier><language>eng</language><publisher>Japan: THE FUKUSHIMA SOCIETY OF MEDICAL SCIENCE</publisher><subject>Adjuvants, Immunologic - pharmacology ; Amino Acid Sequence ; Animals ; autoantibody ; autoimmune hepatitis ; Blotting, Western ; Calreticulin - immunology ; Enzyme-Linked Immunosorbent Assay ; Female ; Hepatitis, Autoimmune - immunology ; hepatocyte ; Humans ; Immune Tolerance ; Immunization ; Interferon-gamma - biosynthesis ; Interleukin-4 - biosynthesis ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Oligodeoxyribonucleotides - pharmacology ; primary biliary cirrhosis ; Western blot</subject><ispartof>FUKUSHIMA JOURNAL OF MEDICAL SCIENCE, 2007, Vol.53(2), pp.95-108</ispartof><rights>2007 The Fukushima Society of Medical Science</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4775-2201899bfdd3371abc6419b470a5b43eb64a04da519ecd21bf27880f151797f13</citedby><cites>FETCH-LOGICAL-c4775-2201899bfdd3371abc6419b470a5b43eb64a04da519ecd21bf27880f151797f13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1877,4010,27900,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18402289$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>ABE, KAZUMICHI</creatorcontrib><creatorcontrib>OHIRA, HIROMASA</creatorcontrib><creatorcontrib>KOBAYASHI, HIROKO</creatorcontrib><creatorcontrib>SAITO, HIRONOBU</creatorcontrib><creatorcontrib>TAKAHASHI, ATSUSHI</creatorcontrib><creatorcontrib>RAI, TSUYOSHI</creatorcontrib><creatorcontrib>KANNO, YUKIKO</creatorcontrib><creatorcontrib>MONOE, KYOKO</creatorcontrib><creatorcontrib>WATANABE, HIROSHI</creatorcontrib><creatorcontrib>IRISAWA, ATSUSHI</creatorcontrib><creatorcontrib>SATO, YUKIO</creatorcontrib><title>BREAKTHROUGH OF IMMUNE SELF-TOLERANCE TO CALRETICULIN INDUCED BY CpG-OLIGODEOXYNUCLEOTIDES AS ADJUVANT</title><title>FUKUSHIMA JOURNAL OF MEDICAL SCIENCE</title><addtitle>Fukushima J. Med. Sci.</addtitle><description>Reportedly, bacterial DNA containing unmethylated cytosine-guanosine dinucleotide motif-containing oligodeoxynucleotides (CpG-ODNs) can induce Th1-type adjuvant effects. We produced autoantibodies and induced hepatitis in mice using extracted proteins from human hepatocytes with CpG-ODNs as adjuvant. Western blot analysis was performed of sera from immunized mice and two patients with autoimmune hepatitis (AIH). When a common band was detected, N-terminal amino acid sequencing was performed to determine its site. For detection of antibodies against the identified protein (calreticulin), ELISA was performed of sera of 50 patients with AIH: 45 with primary biliary cirrhosis (PBC), 24 with chronic hepatitis C (CH), and 24 healthy controls. Mice were immunized with calreticulin protein with CpG-ODNs as adjuvant. Several reacted bands were detected in their sera; in addition, a common band to the sera of patients with AIH was detected at 60 kDa. Subsequent N-terminal amino acid sequencing revealed that the protein was human calreticulin. ELISA showed that, of patients with AIH, PBC, and CH, 30.0% (15/50), 17.8% (8/45), and 12.5% (3/24), respectively, were positive for anti-calreticulin antibodies. Splenocytes from immunized mice produced IFN-γ after they were pulsed with calreticulin protein. Histological analyses of liver specimens taken from mice immunized with calreticulin protein together with CpG-ODN s showed spotty and focal necrosis. Immunofluorescence analysis showed increased expression of calreticulin in the liver treated with CpG-ODNs. These results suggest that a breakthrough of immune self-tolerance to calreticulin is induced with CpG-ODNs as adjuvant and that calreticulin protein might be a target antigen in this model.</description><subject>Adjuvants, Immunologic - pharmacology</subject><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>autoantibody</subject><subject>autoimmune hepatitis</subject><subject>Blotting, Western</subject><subject>Calreticulin - immunology</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Female</subject><subject>Hepatitis, Autoimmune - immunology</subject><subject>hepatocyte</subject><subject>Humans</subject><subject>Immune Tolerance</subject><subject>Immunization</subject><subject>Interferon-gamma - biosynthesis</subject><subject>Interleukin-4 - biosynthesis</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Inbred C57BL</subject><subject>Oligodeoxyribonucleotides - pharmacology</subject><subject>primary biliary cirrhosis</subject><subject>Western blot</subject><issn>0016-2590</issn><issn>2185-4610</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkEFLwzAYhoMobk4P_gHJSfBQTdJkacBL12ZbtWugtqKnkrapbmxuNtvBf29lU-GD7-Xl4Tm8AFxidMtcj981K9uFW8GOQJ9gjzl0iNEx6COEhw5hAvXAmbULhKjgCJ2CHvYoIsQTfdCMUuk_ZtNU5ZMpVGMYzWZ5IuGTjMdOpmKZ-kkgYaZg4MepzKIgj6MERkmYBzKEo1cYbCaOiqOJCqV6eU3yIJYqi0L5BP3uwof82U-yc3DS6KU1F4c_APlYZsHUidUk6sxORTlnDiEIe0KUTV27Lse6rIYUi5JypFlJXVMOqUa01gwLU9UElw3hnocazDAXvMHuAFzvvZt2_bkzdlus5rYyy6X-MOudLTjCLsNUdODNHqzatbWtaYpNO1_p9qvAqPgZtehG7UIhWMdeHaS7cmXqf_KwYgfc74GF3eo38wfodjuvluZXRfa-v7p6121hPtxvFlR_MQ</recordid><startdate>2007</startdate><enddate>2007</enddate><creator>ABE, KAZUMICHI</creator><creator>OHIRA, HIROMASA</creator><creator>KOBAYASHI, HIROKO</creator><creator>SAITO, HIRONOBU</creator><creator>TAKAHASHI, ATSUSHI</creator><creator>RAI, TSUYOSHI</creator><creator>KANNO, YUKIKO</creator><creator>MONOE, KYOKO</creator><creator>WATANABE, HIROSHI</creator><creator>IRISAWA, ATSUSHI</creator><creator>SATO, YUKIO</creator><general>THE FUKUSHIMA SOCIETY OF MEDICAL SCIENCE</general><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></search><sort><creationdate>2007</creationdate><title>BREAKTHROUGH OF IMMUNE SELF-TOLERANCE TO CALRETICULIN INDUCED BY CpG-OLIGODEOXYNUCLEOTIDES AS ADJUVANT</title><author>ABE, KAZUMICHI ; OHIRA, HIROMASA ; KOBAYASHI, HIROKO ; SAITO, HIRONOBU ; TAKAHASHI, ATSUSHI ; RAI, TSUYOSHI ; KANNO, YUKIKO ; MONOE, KYOKO ; WATANABE, HIROSHI ; IRISAWA, ATSUSHI ; SATO, YUKIO</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4775-2201899bfdd3371abc6419b470a5b43eb64a04da519ecd21bf27880f151797f13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adjuvants, Immunologic - pharmacology</topic><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>autoantibody</topic><topic>autoimmune hepatitis</topic><topic>Blotting, Western</topic><topic>Calreticulin - immunology</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Female</topic><topic>Hepatitis, Autoimmune - immunology</topic><topic>hepatocyte</topic><topic>Humans</topic><topic>Immune Tolerance</topic><topic>Immunization</topic><topic>Interferon-gamma - biosynthesis</topic><topic>Interleukin-4 - biosynthesis</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Inbred C57BL</topic><topic>Oligodeoxyribonucleotides - pharmacology</topic><topic>primary biliary cirrhosis</topic><topic>Western blot</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ABE, KAZUMICHI</creatorcontrib><creatorcontrib>OHIRA, HIROMASA</creatorcontrib><creatorcontrib>KOBAYASHI, HIROKO</creatorcontrib><creatorcontrib>SAITO, HIRONOBU</creatorcontrib><creatorcontrib>TAKAHASHI, ATSUSHI</creatorcontrib><creatorcontrib>RAI, TSUYOSHI</creatorcontrib><creatorcontrib>KANNO, YUKIKO</creatorcontrib><creatorcontrib>MONOE, KYOKO</creatorcontrib><creatorcontrib>WATANABE, HIROSHI</creatorcontrib><creatorcontrib>IRISAWA, ATSUSHI</creatorcontrib><creatorcontrib>SATO, YUKIO</creatorcontrib><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><jtitle>FUKUSHIMA JOURNAL OF MEDICAL SCIENCE</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>ABE, KAZUMICHI</au><au>OHIRA, HIROMASA</au><au>KOBAYASHI, HIROKO</au><au>SAITO, HIRONOBU</au><au>TAKAHASHI, ATSUSHI</au><au>RAI, TSUYOSHI</au><au>KANNO, YUKIKO</au><au>MONOE, KYOKO</au><au>WATANABE, HIROSHI</au><au>IRISAWA, ATSUSHI</au><au>SATO, YUKIO</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>BREAKTHROUGH OF IMMUNE SELF-TOLERANCE TO CALRETICULIN INDUCED BY CpG-OLIGODEOXYNUCLEOTIDES AS ADJUVANT</atitle><jtitle>FUKUSHIMA JOURNAL OF MEDICAL SCIENCE</jtitle><addtitle>Fukushima J. Med. Sci.</addtitle><date>2007</date><risdate>2007</risdate><volume>53</volume><issue>2</issue><spage>95</spage><epage>108</epage><pages>95-108</pages><issn>0016-2590</issn><eissn>2185-4610</eissn><abstract>Reportedly, bacterial DNA containing unmethylated cytosine-guanosine dinucleotide motif-containing oligodeoxynucleotides (CpG-ODNs) can induce Th1-type adjuvant effects. We produced autoantibodies and induced hepatitis in mice using extracted proteins from human hepatocytes with CpG-ODNs as adjuvant. Western blot analysis was performed of sera from immunized mice and two patients with autoimmune hepatitis (AIH). When a common band was detected, N-terminal amino acid sequencing was performed to determine its site. For detection of antibodies against the identified protein (calreticulin), ELISA was performed of sera of 50 patients with AIH: 45 with primary biliary cirrhosis (PBC), 24 with chronic hepatitis C (CH), and 24 healthy controls. Mice were immunized with calreticulin protein with CpG-ODNs as adjuvant. Several reacted bands were detected in their sera; in addition, a common band to the sera of patients with AIH was detected at 60 kDa. Subsequent N-terminal amino acid sequencing revealed that the protein was human calreticulin. ELISA showed that, of patients with AIH, PBC, and CH, 30.0% (15/50), 17.8% (8/45), and 12.5% (3/24), respectively, were positive for anti-calreticulin antibodies. Splenocytes from immunized mice produced IFN-γ after they were pulsed with calreticulin protein. Histological analyses of liver specimens taken from mice immunized with calreticulin protein together with CpG-ODN s showed spotty and focal necrosis. Immunofluorescence analysis showed increased expression of calreticulin in the liver treated with CpG-ODNs. These results suggest that a breakthrough of immune self-tolerance to calreticulin is induced with CpG-ODNs as adjuvant and that calreticulin protein might be a target antigen in this model.</abstract><cop>Japan</cop><pub>THE FUKUSHIMA SOCIETY OF MEDICAL SCIENCE</pub><pmid>18402289</pmid><doi>10.5387/fms.53.95</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adjuvants, Immunologic - pharmacology Amino Acid Sequence Animals autoantibody autoimmune hepatitis Blotting, Western Calreticulin - immunology Enzyme-Linked Immunosorbent Assay Female Hepatitis, Autoimmune - immunology hepatocyte Humans Immune Tolerance Immunization Interferon-gamma - biosynthesis Interleukin-4 - biosynthesis Mice Mice, Inbred BALB C Mice, Inbred C57BL Oligodeoxyribonucleotides - pharmacology primary biliary cirrhosis Western blot |
title | BREAKTHROUGH OF IMMUNE SELF-TOLERANCE TO CALRETICULIN INDUCED BY CpG-OLIGODEOXYNUCLEOTIDES AS ADJUVANT |
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