BP180 ELISA using bacterial recombinant NC16a protein as a diagnostic and monitoring tool for bullous pemphigoid
Bullous pemphigoid (BP) is an acquired autoimmune subepidermal blistering disease against hemidesmosomal cytoplasmic BP230 and transmembrane BP180 proteins. Epitope mapping studies have shown that the membrane-proximal noncollagenous (NC) 16a domain of BP180 harbors clusters of antigenic sites recog...
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Veröffentlicht in: | Journal of dermatological science 2002-12, Vol.30 (3), p.224-232 |
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creator | Kobayashi, Masakazu Amagai, Masayuki Kuroda-Kinoshita, Keiko Hashimoto, Takashi Shirakata, Yuji Hashimoto, Koji Nishikawa, Takeji |
description | Bullous pemphigoid (BP) is an acquired autoimmune subepidermal blistering disease against hemidesmosomal cytoplasmic BP230 and transmembrane BP180 proteins. Epitope mapping studies have shown that the membrane-proximal noncollagenous (NC) 16a domain of BP180 harbors clusters of antigenic sites recognized by the vast majority of BP sera. In this study, we developed an enzyme-linked immunosorbent assay (ELISA) using bacterial recombinant NC16a protein and evaluated its clinical benefit for diagnosis and monitoring disease activity. Fifty four (84.4%) of 64 sera from BP patients were positive, while only one (1.1%) of 91 sera from collagen disease patients and five (1.5%) of 336 sera from normal control barely exceeded the cut-off value. None of 69 pemphigus vulgaris sera and none of 42 pemphigus foliaceus sera exceeded the cut-off value. Thus, the sensitivity and specificity of NC16a ELISA were 84.4 and 98.9%, respectively. The correlation between ELISA scores and disease activity along the time course was examined using seven BP patients. NC16a ELISA scores tended to fluctuate in parallel with the disease activity along the time course and reflected the disease activity much better than indirect immunofluorescence. These findings indicate that NC16a ELISA will be a valuable tool not only for the diagnosis of patients with BP but also for the monitoring of the disease activity. |
doi_str_mv | 10.1016/s0923-1811(02)00109-3 |
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Epitope mapping studies have shown that the membrane-proximal noncollagenous (NC) 16a domain of BP180 harbors clusters of antigenic sites recognized by the vast majority of BP sera. In this study, we developed an enzyme-linked immunosorbent assay (ELISA) using bacterial recombinant NC16a protein and evaluated its clinical benefit for diagnosis and monitoring disease activity. Fifty four (84.4%) of 64 sera from BP patients were positive, while only one (1.1%) of 91 sera from collagen disease patients and five (1.5%) of 336 sera from normal control barely exceeded the cut-off value. None of 69 pemphigus vulgaris sera and none of 42 pemphigus foliaceus sera exceeded the cut-off value. Thus, the sensitivity and specificity of NC16a ELISA were 84.4 and 98.9%, respectively. The correlation between ELISA scores and disease activity along the time course was examined using seven BP patients. NC16a ELISA scores tended to fluctuate in parallel with the disease activity along the time course and reflected the disease activity much better than indirect immunofluorescence. These findings indicate that NC16a ELISA will be a valuable tool not only for the diagnosis of patients with BP but also for the monitoring of the disease activity.</description><identifier>ISSN: 0923-1811</identifier><identifier>DOI: 10.1016/s0923-1811(02)00109-3</identifier><identifier>PMID: 12443845</identifier><language>eng</language><publisher>Netherlands</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Autoantigens - chemistry ; Bacterial Proteins ; Carrier Proteins ; Case-Control Studies ; Collagen - chemistry ; Collagen Diseases - immunology ; Collagen Type XVII ; Cytoskeletal Proteins ; Dystonin ; Enzyme-Linked Immunosorbent Assay - methods ; Female ; Humans ; Male ; Middle Aged ; Nerve Tissue Proteins ; Non-Fibrillar Collagens ; Pemphigoid, Bullous - diagnosis ; Pemphigoid, Bullous - immunology ; Pemphigoid, Bullous - physiopathology ; Protein Structure, Tertiary - physiology ; Recombinant Proteins ; Sensitivity and Specificity</subject><ispartof>Journal of dermatological science, 2002-12, Vol.30 (3), p.224-232</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c476t-add8e72d4950b489e3f4187ed333b191cbd7595a4c47edb5f4b1560eaab34d823</citedby><cites>FETCH-LOGICAL-c476t-add8e72d4950b489e3f4187ed333b191cbd7595a4c47edb5f4b1560eaab34d823</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12443845$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kobayashi, Masakazu</creatorcontrib><creatorcontrib>Amagai, Masayuki</creatorcontrib><creatorcontrib>Kuroda-Kinoshita, Keiko</creatorcontrib><creatorcontrib>Hashimoto, Takashi</creatorcontrib><creatorcontrib>Shirakata, Yuji</creatorcontrib><creatorcontrib>Hashimoto, Koji</creatorcontrib><creatorcontrib>Nishikawa, Takeji</creatorcontrib><title>BP180 ELISA using bacterial recombinant NC16a protein as a diagnostic and monitoring tool for bullous pemphigoid</title><title>Journal of dermatological science</title><addtitle>J Dermatol Sci</addtitle><description>Bullous pemphigoid (BP) is an acquired autoimmune subepidermal blistering disease against hemidesmosomal cytoplasmic BP230 and transmembrane BP180 proteins. Epitope mapping studies have shown that the membrane-proximal noncollagenous (NC) 16a domain of BP180 harbors clusters of antigenic sites recognized by the vast majority of BP sera. In this study, we developed an enzyme-linked immunosorbent assay (ELISA) using bacterial recombinant NC16a protein and evaluated its clinical benefit for diagnosis and monitoring disease activity. Fifty four (84.4%) of 64 sera from BP patients were positive, while only one (1.1%) of 91 sera from collagen disease patients and five (1.5%) of 336 sera from normal control barely exceeded the cut-off value. None of 69 pemphigus vulgaris sera and none of 42 pemphigus foliaceus sera exceeded the cut-off value. Thus, the sensitivity and specificity of NC16a ELISA were 84.4 and 98.9%, respectively. The correlation between ELISA scores and disease activity along the time course was examined using seven BP patients. NC16a ELISA scores tended to fluctuate in parallel with the disease activity along the time course and reflected the disease activity much better than indirect immunofluorescence. These findings indicate that NC16a ELISA will be a valuable tool not only for the diagnosis of patients with BP but also for the monitoring of the disease activity.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Autoantigens - chemistry</subject><subject>Bacterial Proteins</subject><subject>Carrier Proteins</subject><subject>Case-Control Studies</subject><subject>Collagen - chemistry</subject><subject>Collagen Diseases - immunology</subject><subject>Collagen Type XVII</subject><subject>Cytoskeletal Proteins</subject><subject>Dystonin</subject><subject>Enzyme-Linked Immunosorbent Assay - methods</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Nerve Tissue Proteins</subject><subject>Non-Fibrillar Collagens</subject><subject>Pemphigoid, Bullous - diagnosis</subject><subject>Pemphigoid, Bullous - immunology</subject><subject>Pemphigoid, Bullous - physiopathology</subject><subject>Protein Structure, Tertiary - physiology</subject><subject>Recombinant Proteins</subject><subject>Sensitivity and Specificity</subject><issn>0923-1811</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkMFPwyAYxTlo3Jz-CRpORg9VKNDCcS5TlyxqMj0TKHRiWqjQHvzv7dyipy95ee99Lz8ALjC6xQgXdwmJnGSYY3yN8huEMBIZOQLTP3kCTlP6RAixnIoTMME5pYRTNgXd_SvmCC7Xq80cDsn5LdSq6m10qoHRVqHVzivfw-cFLhTsYuit81AlqKBxautD6l0FlTewDd71Ie4q-hAaWIcI9dA0YUiws2334bbBmTNwXKsm2fPDnYH3h-Xb4ilbvzyuFvN1VtGy6DNlDLdlbqhgSFMuLKkp5qU1hBCNBa60KZlgio52azSrqcasQFYpTajhOZmBq33vOPlrsKmXrUuVbRrl7bhIlnnBueBsNLK9sYohpWhr2UXXqvgtMZI7vHKz4yh3HCXK5S9eScbc5eHBoFtr_lMHtuQHYIN4QA</recordid><startdate>200212</startdate><enddate>200212</enddate><creator>Kobayashi, Masakazu</creator><creator>Amagai, Masayuki</creator><creator>Kuroda-Kinoshita, Keiko</creator><creator>Hashimoto, Takashi</creator><creator>Shirakata, Yuji</creator><creator>Hashimoto, Koji</creator><creator>Nishikawa, Takeji</creator><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>200212</creationdate><title>BP180 ELISA using bacterial recombinant NC16a protein as a diagnostic and monitoring tool for bullous pemphigoid</title><author>Kobayashi, Masakazu ; Amagai, Masayuki ; Kuroda-Kinoshita, Keiko ; Hashimoto, Takashi ; Shirakata, Yuji ; Hashimoto, Koji ; Nishikawa, Takeji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c476t-add8e72d4950b489e3f4187ed333b191cbd7595a4c47edb5f4b1560eaab34d823</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Autoantigens - chemistry</topic><topic>Bacterial Proteins</topic><topic>Carrier Proteins</topic><topic>Case-Control Studies</topic><topic>Collagen - chemistry</topic><topic>Collagen Diseases - immunology</topic><topic>Collagen Type XVII</topic><topic>Cytoskeletal Proteins</topic><topic>Dystonin</topic><topic>Enzyme-Linked Immunosorbent Assay - methods</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Nerve Tissue Proteins</topic><topic>Non-Fibrillar Collagens</topic><topic>Pemphigoid, Bullous - diagnosis</topic><topic>Pemphigoid, Bullous - immunology</topic><topic>Pemphigoid, Bullous - physiopathology</topic><topic>Protein Structure, Tertiary - physiology</topic><topic>Recombinant Proteins</topic><topic>Sensitivity and Specificity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kobayashi, Masakazu</creatorcontrib><creatorcontrib>Amagai, Masayuki</creatorcontrib><creatorcontrib>Kuroda-Kinoshita, Keiko</creatorcontrib><creatorcontrib>Hashimoto, Takashi</creatorcontrib><creatorcontrib>Shirakata, Yuji</creatorcontrib><creatorcontrib>Hashimoto, Koji</creatorcontrib><creatorcontrib>Nishikawa, Takeji</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>Journal of dermatological science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kobayashi, Masakazu</au><au>Amagai, Masayuki</au><au>Kuroda-Kinoshita, Keiko</au><au>Hashimoto, Takashi</au><au>Shirakata, Yuji</au><au>Hashimoto, Koji</au><au>Nishikawa, Takeji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>BP180 ELISA using bacterial recombinant NC16a protein as a diagnostic and monitoring tool for bullous pemphigoid</atitle><jtitle>Journal of dermatological science</jtitle><addtitle>J Dermatol Sci</addtitle><date>2002-12</date><risdate>2002</risdate><volume>30</volume><issue>3</issue><spage>224</spage><epage>232</epage><pages>224-232</pages><issn>0923-1811</issn><abstract>Bullous pemphigoid (BP) is an acquired autoimmune subepidermal blistering disease against hemidesmosomal cytoplasmic BP230 and transmembrane BP180 proteins. Epitope mapping studies have shown that the membrane-proximal noncollagenous (NC) 16a domain of BP180 harbors clusters of antigenic sites recognized by the vast majority of BP sera. In this study, we developed an enzyme-linked immunosorbent assay (ELISA) using bacterial recombinant NC16a protein and evaluated its clinical benefit for diagnosis and monitoring disease activity. Fifty four (84.4%) of 64 sera from BP patients were positive, while only one (1.1%) of 91 sera from collagen disease patients and five (1.5%) of 336 sera from normal control barely exceeded the cut-off value. None of 69 pemphigus vulgaris sera and none of 42 pemphigus foliaceus sera exceeded the cut-off value. Thus, the sensitivity and specificity of NC16a ELISA were 84.4 and 98.9%, respectively. The correlation between ELISA scores and disease activity along the time course was examined using seven BP patients. NC16a ELISA scores tended to fluctuate in parallel with the disease activity along the time course and reflected the disease activity much better than indirect immunofluorescence. These findings indicate that NC16a ELISA will be a valuable tool not only for the diagnosis of patients with BP but also for the monitoring of the disease activity.</abstract><cop>Netherlands</cop><pmid>12443845</pmid><doi>10.1016/s0923-1811(02)00109-3</doi><tpages>9</tpages></addata></record> |
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subjects | Adult Aged Aged, 80 and over Autoantigens - chemistry Bacterial Proteins Carrier Proteins Case-Control Studies Collagen - chemistry Collagen Diseases - immunology Collagen Type XVII Cytoskeletal Proteins Dystonin Enzyme-Linked Immunosorbent Assay - methods Female Humans Male Middle Aged Nerve Tissue Proteins Non-Fibrillar Collagens Pemphigoid, Bullous - diagnosis Pemphigoid, Bullous - immunology Pemphigoid, Bullous - physiopathology Protein Structure, Tertiary - physiology Recombinant Proteins Sensitivity and Specificity |
title | BP180 ELISA using bacterial recombinant NC16a protein as a diagnostic and monitoring tool for bullous pemphigoid |
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