Exposure of Mice to Topical Bovine Thrombin Induces Systemic Autoimmunity
Bovine thrombin is used as an aid to hemostasis in medical and surgical procedures. At least 500,000 Americans are exposed to this therapeutic annually and reports suggest that exposure is associated with the development of autoreactive antibodies. To determine whether bovine thrombin can induce pat...
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Veröffentlicht in: | The American journal of pathology 2001-11, Vol.159 (5), p.1957-1969 |
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container_end_page | 1969 |
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container_issue | 5 |
container_start_page | 1957 |
container_title | The American journal of pathology |
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creator | Schoenecker, Jonathan G. Johnson, Rachel K. Lesher, Aaron P. Day, Jarrod D. Love, Stephanie D. Hoffman, Maureane R. Ortel, Thomas L. Parker, William Lawson, Jeffrey H. |
description | Bovine thrombin is used as an aid to hemostasis in medical and surgical procedures. At least 500,000 Americans are exposed to this therapeutic annually and reports suggest that exposure is associated with the development of autoreactive antibodies. To determine whether bovine thrombin can induce pathological autoimmunity we exposed nonautoimmune-prone galactose-α1-3-galactose-deficient mice to the two bovine thrombin preparations currently approved for use in the United States. We found that, like humans exposed to bovine thrombin, mice developed an immune response against the therapeutic and the xenogeneic carbohydrate galactose-α1-3-galactose, and some mice developed autoantibodies against clotting factors. Further, unexpectedly, a single exposure to this therapeutic also induced autoimmunity with features characteristic of systemic lupus erythematosus including antibodies against nuclear antigens, native DNA, double-stranded DNA, and cardiolipin. High levels of these autoantibodies correlated with glomerulonephritis in all mice evaluated. This autoimmune syndrome was detected in mice 15 weeks after a secondary exposure to bovine thrombin and female mice were found to develop the syndrome at a significantly greater frequency than males. Thus, these studies indicate that exposure to bovine thrombin preparations can induce a pathological systemic autoimmune syndrome with lupus-like serology. |
doi_str_mv | 10.1016/S0002-9440(10)63043-X |
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At least 500,000 Americans are exposed to this therapeutic annually and reports suggest that exposure is associated with the development of autoreactive antibodies. To determine whether bovine thrombin can induce pathological autoimmunity we exposed nonautoimmune-prone galactose-α1-3-galactose-deficient mice to the two bovine thrombin preparations currently approved for use in the United States. We found that, like humans exposed to bovine thrombin, mice developed an immune response against the therapeutic and the xenogeneic carbohydrate galactose-α1-3-galactose, and some mice developed autoantibodies against clotting factors. Further, unexpectedly, a single exposure to this therapeutic also induced autoimmunity with features characteristic of systemic lupus erythematosus including antibodies against nuclear antigens, native DNA, double-stranded DNA, and cardiolipin. High levels of these autoantibodies correlated with glomerulonephritis in all mice evaluated. This autoimmune syndrome was detected in mice 15 weeks after a secondary exposure to bovine thrombin and female mice were found to develop the syndrome at a significantly greater frequency than males. Thus, these studies indicate that exposure to bovine thrombin preparations can induce a pathological systemic autoimmune syndrome with lupus-like serology.</description><identifier>ISSN: 0002-9440</identifier><identifier>EISSN: 1525-2191</identifier><identifier>DOI: 10.1016/S0002-9440(10)63043-X</identifier><identifier>PMID: 11696457</identifier><identifier>CODEN: AJPAA4</identifier><language>eng</language><publisher>Bethesda, MD: Elsevier Inc</publisher><subject>Administration, Topical ; Animal Model ; Animals ; Antibodies - immunology ; Antibodies, Anticardiolipin - biosynthesis ; Antibodies, Antinuclear - analysis ; Autoantibodies - immunology ; Autoimmune Diseases - immunology ; Autoimmune Diseases - pathology ; Autoimmune Diseases - psychology ; Autoimmunity - immunology ; Behavior, Animal ; Biological and medical sciences ; Cattle ; DNA - immunology ; DNA, Single-Stranded - immunology ; Experimental and animal immunopathology. Animal models ; Female ; Galactosyltransferases - genetics ; Galactosyltransferases - immunology ; Immunopathology ; Male ; Medical sciences ; Mice ; Mice, Knockout - genetics ; Microscopy, Electron ; Thrombin - administration & dosage ; Thrombin - immunology ; Time Factors</subject><ispartof>The American journal of pathology, 2001-11, Vol.159 (5), p.1957-1969</ispartof><rights>2001 American Society for Investigative Pathology</rights><rights>2002 INIST-CNRS</rights><rights>Copyright American Society for Investigative Pathology Nov 2001</rights><rights>Copyright © 2001, American Society for Investigative Pathology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c552t-d0c02d7fd381909989b22ec60a2f4538b9c4254c1a11c5abd4a5131b02c47cc83</citedby><cites>FETCH-LOGICAL-c552t-d0c02d7fd381909989b22ec60a2f4538b9c4254c1a11c5abd4a5131b02c47cc83</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/PMC1867043/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S000294401063043X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,3537,27901,27902,53766,53768,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14130795$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11696457$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schoenecker, Jonathan G.</creatorcontrib><creatorcontrib>Johnson, Rachel K.</creatorcontrib><creatorcontrib>Lesher, Aaron P.</creatorcontrib><creatorcontrib>Day, Jarrod D.</creatorcontrib><creatorcontrib>Love, Stephanie D.</creatorcontrib><creatorcontrib>Hoffman, Maureane R.</creatorcontrib><creatorcontrib>Ortel, Thomas L.</creatorcontrib><creatorcontrib>Parker, William</creatorcontrib><creatorcontrib>Lawson, Jeffrey H.</creatorcontrib><title>Exposure of Mice to Topical Bovine Thrombin Induces Systemic Autoimmunity</title><title>The American journal of pathology</title><addtitle>Am J Pathol</addtitle><description>Bovine thrombin is used as an aid to hemostasis in medical and surgical procedures. At least 500,000 Americans are exposed to this therapeutic annually and reports suggest that exposure is associated with the development of autoreactive antibodies. To determine whether bovine thrombin can induce pathological autoimmunity we exposed nonautoimmune-prone galactose-α1-3-galactose-deficient mice to the two bovine thrombin preparations currently approved for use in the United States. We found that, like humans exposed to bovine thrombin, mice developed an immune response against the therapeutic and the xenogeneic carbohydrate galactose-α1-3-galactose, and some mice developed autoantibodies against clotting factors. Further, unexpectedly, a single exposure to this therapeutic also induced autoimmunity with features characteristic of systemic lupus erythematosus including antibodies against nuclear antigens, native DNA, double-stranded DNA, and cardiolipin. High levels of these autoantibodies correlated with glomerulonephritis in all mice evaluated. This autoimmune syndrome was detected in mice 15 weeks after a secondary exposure to bovine thrombin and female mice were found to develop the syndrome at a significantly greater frequency than males. Thus, these studies indicate that exposure to bovine thrombin preparations can induce a pathological systemic autoimmune syndrome with lupus-like serology.</description><subject>Administration, Topical</subject><subject>Animal Model</subject><subject>Animals</subject><subject>Antibodies - immunology</subject><subject>Antibodies, Anticardiolipin - biosynthesis</subject><subject>Antibodies, Antinuclear - analysis</subject><subject>Autoantibodies - immunology</subject><subject>Autoimmune Diseases - immunology</subject><subject>Autoimmune Diseases - pathology</subject><subject>Autoimmune Diseases - psychology</subject><subject>Autoimmunity - immunology</subject><subject>Behavior, Animal</subject><subject>Biological and medical sciences</subject><subject>Cattle</subject><subject>DNA - immunology</subject><subject>DNA, Single-Stranded - immunology</subject><subject>Experimental and animal immunopathology. 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At least 500,000 Americans are exposed to this therapeutic annually and reports suggest that exposure is associated with the development of autoreactive antibodies. To determine whether bovine thrombin can induce pathological autoimmunity we exposed nonautoimmune-prone galactose-α1-3-galactose-deficient mice to the two bovine thrombin preparations currently approved for use in the United States. We found that, like humans exposed to bovine thrombin, mice developed an immune response against the therapeutic and the xenogeneic carbohydrate galactose-α1-3-galactose, and some mice developed autoantibodies against clotting factors. Further, unexpectedly, a single exposure to this therapeutic also induced autoimmunity with features characteristic of systemic lupus erythematosus including antibodies against nuclear antigens, native DNA, double-stranded DNA, and cardiolipin. High levels of these autoantibodies correlated with glomerulonephritis in all mice evaluated. This autoimmune syndrome was detected in mice 15 weeks after a secondary exposure to bovine thrombin and female mice were found to develop the syndrome at a significantly greater frequency than males. Thus, these studies indicate that exposure to bovine thrombin preparations can induce a pathological systemic autoimmune syndrome with lupus-like serology.</abstract><cop>Bethesda, MD</cop><pub>Elsevier Inc</pub><pmid>11696457</pmid><doi>10.1016/S0002-9440(10)63043-X</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Administration, Topical Animal Model Animals Antibodies - immunology Antibodies, Anticardiolipin - biosynthesis Antibodies, Antinuclear - analysis Autoantibodies - immunology Autoimmune Diseases - immunology Autoimmune Diseases - pathology Autoimmune Diseases - psychology Autoimmunity - immunology Behavior, Animal Biological and medical sciences Cattle DNA - immunology DNA, Single-Stranded - immunology Experimental and animal immunopathology. Animal models Female Galactosyltransferases - genetics Galactosyltransferases - immunology Immunopathology Male Medical sciences Mice Mice, Knockout - genetics Microscopy, Electron Thrombin - administration & dosage Thrombin - immunology Time Factors |
title | Exposure of Mice to Topical Bovine Thrombin Induces Systemic Autoimmunity |
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