Tissue-specific effects of an anti-desmoglein-3 ADCC antibody due to expression of the target antigen and physiological characteristics of the mouse vagina
Desmoglein-3 (DSG3) is a potential target of cytotoxic antibody therapy for squamous cell carcinomas but is also expressed in various normal squamous epithelia. We obtained information about DSG3 distribution in mouse tissues by immunohistochemistry and conducted an intravenous multiple-dose study i...
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Veröffentlicht in: | Journal of Toxicologic Pathology 2020, Vol.33(2), pp.67-76 |
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description | Desmoglein-3 (DSG3) is a potential target of cytotoxic antibody therapy for squamous cell carcinomas but is also expressed in various normal squamous epithelia. We obtained information about DSG3 distribution in mouse tissues by immunohistochemistry and conducted an intravenous multiple-dose study in mouse to estimate the toxic potential of anti-DSG3 therapy. DSG3 was expressed in the squamous epithelium of several organs including the skin, esophagus, tongue, forestomach, eye, and vagina. It was expressed at all estrous cycles of the vagina with changes in distribution patterns along with the structural changes in each cycle, and expression was reduced in ovariectomized (OVX) mice. On the administration of the antibody, there was disarrangement of the vaginal mucosal epithelium with formation of miroabscess, increased granulocyte infiltration, and single cell necrosis. Despite similar expression levels of DSG3 in other tissues, histopathological changes were limited to the vagina. The severity of the changes was reduced by ovariectomy. From these findings, the lesions were thought to be related to the drastic change in the histological structure of the vaginal mucosa accompanying the estrous cycle. Thus, we have shown that the changing expression of target antigen distribution and its relationship with physiological changes in tissue structure are important features for estimating the toxic potential of cytotoxic antibody therapy. |
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We obtained information about DSG3 distribution in mouse tissues by immunohistochemistry and conducted an intravenous multiple-dose study in mouse to estimate the toxic potential of anti-DSG3 therapy. DSG3 was expressed in the squamous epithelium of several organs including the skin, esophagus, tongue, forestomach, eye, and vagina. It was expressed at all estrous cycles of the vagina with changes in distribution patterns along with the structural changes in each cycle, and expression was reduced in ovariectomized (OVX) mice. On the administration of the antibody, there was disarrangement of the vaginal mucosal epithelium with formation of miroabscess, increased granulocyte infiltration, and single cell necrosis. Despite similar expression levels of DSG3 in other tissues, histopathological changes were limited to the vagina. The severity of the changes was reduced by ovariectomy. From these findings, the lesions were thought to be related to the drastic change in the histological structure of the vaginal mucosa accompanying the estrous cycle. Thus, we have shown that the changing expression of target antigen distribution and its relationship with physiological changes in tissue structure are important features for estimating the toxic potential of cytotoxic antibody therapy.</description><identifier>ISSN: 0914-9198</identifier><identifier>EISSN: 1881-915X</identifier><identifier>EISSN: 1347-7404</identifier><identifier>DOI: 10.1293/tox.2019-0040</identifier><identifier>PMID: 32425339</identifier><language>eng</language><publisher>Japan: JAPANESE SOCIETY OF TOXICOLOGIC PATHOLOGY</publisher><subject>Animal tissues ; Antibodies ; Antigens ; cytotoxic antibody ; Cytotoxicity ; Desmoglein 3 ; Epithelium ; Esophagus ; estrous cycle ; Estrus cycle ; Immunohistochemistry ; Immunotherapy ; Intravenous administration ; Leukocytes (granulocytic) ; Mucosa ; Necrosis ; Organs ; Original ; Ovariectomy ; Physiology ; Squamous cell carcinoma ; Therapy ; tissue distribution ; Vagina</subject><ispartof>Journal of Toxicologic Pathology, 2020, Vol.33(2), pp.67-76</ispartof><rights>2020 The Japanese Society of Toxicologic Pathology</rights><rights>2020 The Japanese Society of Toxicologic Pathology.</rights><rights>Copyright Japan Science and Technology Agency 2020</rights><rights>2020 The Japanese Society of Toxicologic Pathology 2020</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c757t-c19b1d168b28bcceb8d5b40886176d442c1c8feaa417fe32dbf9390e7df930843</citedby><cites>FETCH-LOGICAL-c757t-c19b1d168b28bcceb8d5b40886176d442c1c8feaa417fe32dbf9390e7df930843</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/PMC7218237/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7218237/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,1883,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32425339$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fujii, Etsuko</creatorcontrib><creatorcontrib>Funahashi, Shinichi</creatorcontrib><creatorcontrib>Taniguchi, Kenji</creatorcontrib><creatorcontrib>Kawai, Shigeto</creatorcontrib><creatorcontrib>Nakano, Kiyotaka</creatorcontrib><creatorcontrib>Kato, Atsuhiko</creatorcontrib><creatorcontrib>Suzuki, Masami</creatorcontrib><creatorcontrib>Chugai Pharmaceutical Co</creatorcontrib><creatorcontrib>The University of Tokyo</creatorcontrib><creatorcontrib>Komaba Open Laboratory</creatorcontrib><creatorcontrib>Ltd</creatorcontrib><creatorcontrib>Forerunner Pharma Research Co</creatorcontrib><title>Tissue-specific effects of an anti-desmoglein-3 ADCC antibody due to expression of the target antigen and physiological characteristics of the mouse vagina</title><title>Journal of Toxicologic Pathology</title><addtitle>J Toxicol Pathol</addtitle><description>Desmoglein-3 (DSG3) is a potential target of cytotoxic antibody therapy for squamous cell carcinomas but is also expressed in various normal squamous epithelia. We obtained information about DSG3 distribution in mouse tissues by immunohistochemistry and conducted an intravenous multiple-dose study in mouse to estimate the toxic potential of anti-DSG3 therapy. DSG3 was expressed in the squamous epithelium of several organs including the skin, esophagus, tongue, forestomach, eye, and vagina. It was expressed at all estrous cycles of the vagina with changes in distribution patterns along with the structural changes in each cycle, and expression was reduced in ovariectomized (OVX) mice. On the administration of the antibody, there was disarrangement of the vaginal mucosal epithelium with formation of miroabscess, increased granulocyte infiltration, and single cell necrosis. Despite similar expression levels of DSG3 in other tissues, histopathological changes were limited to the vagina. The severity of the changes was reduced by ovariectomy. From these findings, the lesions were thought to be related to the drastic change in the histological structure of the vaginal mucosa accompanying the estrous cycle. Thus, we have shown that the changing expression of target antigen distribution and its relationship with physiological changes in tissue structure are important features for estimating the toxic potential of cytotoxic antibody therapy.</description><subject>Animal tissues</subject><subject>Antibodies</subject><subject>Antigens</subject><subject>cytotoxic antibody</subject><subject>Cytotoxicity</subject><subject>Desmoglein 3</subject><subject>Epithelium</subject><subject>Esophagus</subject><subject>estrous cycle</subject><subject>Estrus cycle</subject><subject>Immunohistochemistry</subject><subject>Immunotherapy</subject><subject>Intravenous administration</subject><subject>Leukocytes (granulocytic)</subject><subject>Mucosa</subject><subject>Necrosis</subject><subject>Organs</subject><subject>Original</subject><subject>Ovariectomy</subject><subject>Physiology</subject><subject>Squamous cell carcinoma</subject><subject>Therapy</subject><subject>tissue distribution</subject><subject>Vagina</subject><issn>0914-9198</issn><issn>1881-915X</issn><issn>1347-7404</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNpdkU1v1DAQhiMEokvhyBVF4sIlxV9J7AtStUBBqsSlSNwsx55kvcrawXaq7m_hz-LsdpcPyfZYnsevZ_wWxWuMrjAR9H3yD1cEYVEhxNCTYoU5x5XA9Y-nxQoJzPJe8IviRYxbhEiLavq8uKCEkZpSsSp-3dkYZ6jiBNr2VpfQ96BTLH1fKpdHspWBuPPDCNZVtLz-uF4fjjtv9qWZoUy-hIcpQIzWu-Ve2uRDFQZIB3CARceU02afidEPVqux1BsVlE4QbExWx9O9nZ8jlPdqsE69LJ71aozw6jFeFt8_f7pbf6luv918XV_fVrqt21RpLDpscMM7wjutoeOm7hjivMFtYxgjGmveg1IMtz1QYrpeUIGgNTkizuhl8eGoO83dDowGl4Ia5RTsToW99MrKfzPObuTg72VLMCe0zQLvHgWC_zlDTHJno4ZxVA5yP5IwxBqGMeEZffsfuvVzcLk9SahoCWMU0UxVR0oHH2OA_lwMRnKxXWbb5WK7XGzP_Ju_OzjTJ58zcHMEcnb5fu9G6-DP28bQrDiprElQ1qQUkRxwnk2bl7ahNRaCLp-1PiptY1IDnJ9SIds4wqEwSiU5LKcCz9nFdQmO_gYoTtqC</recordid><startdate>20200101</startdate><enddate>20200101</enddate><creator>Fujii, Etsuko</creator><creator>Funahashi, Shinichi</creator><creator>Taniguchi, Kenji</creator><creator>Kawai, Shigeto</creator><creator>Nakano, Kiyotaka</creator><creator>Kato, Atsuhiko</creator><creator>Suzuki, Masami</creator><general>JAPANESE SOCIETY OF TOXICOLOGIC PATHOLOGY</general><general>The Japanese Society of Toxicologic Pathology</general><general>Japan Science and Technology Agency</general><general>Japanese Society of Toxicologic Pathology</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U7</scope><scope>C1K</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20200101</creationdate><title>Tissue-specific effects of an anti-desmoglein-3 ADCC antibody due to expression of the target antigen and physiological characteristics of the mouse vagina</title><author>Fujii, Etsuko ; Funahashi, Shinichi ; Taniguchi, Kenji ; Kawai, Shigeto ; Nakano, Kiyotaka ; Kato, Atsuhiko ; Suzuki, Masami</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c757t-c19b1d168b28bcceb8d5b40886176d442c1c8feaa417fe32dbf9390e7df930843</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animal tissues</topic><topic>Antibodies</topic><topic>Antigens</topic><topic>cytotoxic antibody</topic><topic>Cytotoxicity</topic><topic>Desmoglein 3</topic><topic>Epithelium</topic><topic>Esophagus</topic><topic>estrous cycle</topic><topic>Estrus cycle</topic><topic>Immunohistochemistry</topic><topic>Immunotherapy</topic><topic>Intravenous administration</topic><topic>Leukocytes (granulocytic)</topic><topic>Mucosa</topic><topic>Necrosis</topic><topic>Organs</topic><topic>Original</topic><topic>Ovariectomy</topic><topic>Physiology</topic><topic>Squamous cell carcinoma</topic><topic>Therapy</topic><topic>tissue distribution</topic><topic>Vagina</topic><toplevel>online_resources</toplevel><creatorcontrib>Fujii, Etsuko</creatorcontrib><creatorcontrib>Funahashi, Shinichi</creatorcontrib><creatorcontrib>Taniguchi, Kenji</creatorcontrib><creatorcontrib>Kawai, Shigeto</creatorcontrib><creatorcontrib>Nakano, Kiyotaka</creatorcontrib><creatorcontrib>Kato, Atsuhiko</creatorcontrib><creatorcontrib>Suzuki, Masami</creatorcontrib><creatorcontrib>Chugai Pharmaceutical Co</creatorcontrib><creatorcontrib>The University of Tokyo</creatorcontrib><creatorcontrib>Komaba Open Laboratory</creatorcontrib><creatorcontrib>Ltd</creatorcontrib><creatorcontrib>Forerunner Pharma Research Co</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of Toxicologic Pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fujii, Etsuko</au><au>Funahashi, Shinichi</au><au>Taniguchi, Kenji</au><au>Kawai, Shigeto</au><au>Nakano, Kiyotaka</au><au>Kato, Atsuhiko</au><au>Suzuki, Masami</au><aucorp>Chugai Pharmaceutical Co</aucorp><aucorp>The University of Tokyo</aucorp><aucorp>Komaba Open Laboratory</aucorp><aucorp>Ltd</aucorp><aucorp>Forerunner Pharma Research Co</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tissue-specific effects of an anti-desmoglein-3 ADCC antibody due to expression of the target antigen and physiological characteristics of the mouse vagina</atitle><jtitle>Journal of Toxicologic Pathology</jtitle><addtitle>J Toxicol Pathol</addtitle><date>2020-01-01</date><risdate>2020</risdate><volume>33</volume><issue>2</issue><spage>67</spage><epage>76</epage><pages>67-76</pages><issn>0914-9198</issn><eissn>1881-915X</eissn><eissn>1347-7404</eissn><abstract>Desmoglein-3 (DSG3) is a potential target of cytotoxic antibody therapy for squamous cell carcinomas but is also expressed in various normal squamous epithelia. We obtained information about DSG3 distribution in mouse tissues by immunohistochemistry and conducted an intravenous multiple-dose study in mouse to estimate the toxic potential of anti-DSG3 therapy. DSG3 was expressed in the squamous epithelium of several organs including the skin, esophagus, tongue, forestomach, eye, and vagina. It was expressed at all estrous cycles of the vagina with changes in distribution patterns along with the structural changes in each cycle, and expression was reduced in ovariectomized (OVX) mice. On the administration of the antibody, there was disarrangement of the vaginal mucosal epithelium with formation of miroabscess, increased granulocyte infiltration, and single cell necrosis. Despite similar expression levels of DSG3 in other tissues, histopathological changes were limited to the vagina. The severity of the changes was reduced by ovariectomy. From these findings, the lesions were thought to be related to the drastic change in the histological structure of the vaginal mucosa accompanying the estrous cycle. Thus, we have shown that the changing expression of target antigen distribution and its relationship with physiological changes in tissue structure are important features for estimating the toxic potential of cytotoxic antibody therapy.</abstract><cop>Japan</cop><pub>JAPANESE SOCIETY OF TOXICOLOGIC PATHOLOGY</pub><pmid>32425339</pmid><doi>10.1293/tox.2019-0040</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animal tissues Antibodies Antigens cytotoxic antibody Cytotoxicity Desmoglein 3 Epithelium Esophagus estrous cycle Estrus cycle Immunohistochemistry Immunotherapy Intravenous administration Leukocytes (granulocytic) Mucosa Necrosis Organs Original Ovariectomy Physiology Squamous cell carcinoma Therapy tissue distribution Vagina |
title | Tissue-specific effects of an anti-desmoglein-3 ADCC antibody due to expression of the target antigen and physiological characteristics of the mouse vagina |
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