Minimal evidence of platelet and endothelial cell reactive antibodies in thrombotic thrombocytopenic purpura
Thrombotic thrombocytopenic purpura (TTP) is a syndrome characterized by microvascular thrombosis with thrombocytopenia and end‐organ injury. Evidence suggests that platelet or endothelial cell injury may be initial pathological events in TTP. A number of factors in patient plasma, including immunog...
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description | Thrombotic thrombocytopenic purpura (TTP) is a syndrome characterized by microvascular thrombosis with thrombocytopenia and end‐organ injury. Evidence suggests that platelet or endothelial cell injury may be initial pathological events in TTP. A number of factors in patient plasma, including immunoglobulins, have been proposed to mediate cellular injury in TTP. However, systematic analyses of TTP patient plasma for the presence of platelet or endothelial cell antibodies are lacking. We, therefore, analyzed 48 TTP patient plasma samples for the presence of platelet and endothelial cell antibodies by using enzyme‐linked immunosorbent assay, flow cytometry, and microlymphocytotoxicity. Twelve of 48 TTP patient samples (25%) reacted against purified platelet glycoproteins. Nine (19%) also contained antibodies that bound to allogeneic target platelets in flow‐cytometric assays. Nine of 48 samples (19%) contained antibodies to human umbilical vein endothelial cells in flow‐cytometric assays, and seven of 48 patient samples (15%) bound to human dermal microvascular endothelial cells. Six of 48 (13%) patient plasma samples contained antibodies that bound to human umbilical vein endothelial cells activated with γ‐interferon and tumor necrosis factor‐α. Of twenty samples that were reactive in one or more platelet or endothelial cell assay, eight contained human leukocyte antigen antibodies reactive in microlymphocytotoxicity. These studies demonstrate that antibodies reactive against platelet or endothelial cell antigens are not prevalent in TTP, and that more than a third of antibodies detected are human leukocyte antigen alloantibodies. Our findings suggest that autoantibodies against platelets or endothelial cells are not important in the pathogenesis of this syndrome. Am. J. Hematol. 62:82–87, 1999. © 1999 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/(SICI)1096-8652(199910)62:2<82::AID-AJH3>3.0.CO;2-H |
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Evidence suggests that platelet or endothelial cell injury may be initial pathological events in TTP. A number of factors in patient plasma, including immunoglobulins, have been proposed to mediate cellular injury in TTP. However, systematic analyses of TTP patient plasma for the presence of platelet or endothelial cell antibodies are lacking. We, therefore, analyzed 48 TTP patient plasma samples for the presence of platelet and endothelial cell antibodies by using enzyme‐linked immunosorbent assay, flow cytometry, and microlymphocytotoxicity. Twelve of 48 TTP patient samples (25%) reacted against purified platelet glycoproteins. Nine (19%) also contained antibodies that bound to allogeneic target platelets in flow‐cytometric assays. Nine of 48 samples (19%) contained antibodies to human umbilical vein endothelial cells in flow‐cytometric assays, and seven of 48 patient samples (15%) bound to human dermal microvascular endothelial cells. Six of 48 (13%) patient plasma samples contained antibodies that bound to human umbilical vein endothelial cells activated with γ‐interferon and tumor necrosis factor‐α. Of twenty samples that were reactive in one or more platelet or endothelial cell assay, eight contained human leukocyte antigen antibodies reactive in microlymphocytotoxicity. These studies demonstrate that antibodies reactive against platelet or endothelial cell antigens are not prevalent in TTP, and that more than a third of antibodies detected are human leukocyte antigen alloantibodies. Our findings suggest that autoantibodies against platelets or endothelial cells are not important in the pathogenesis of this syndrome. Am. J. 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Evidence suggests that platelet or endothelial cell injury may be initial pathological events in TTP. A number of factors in patient plasma, including immunoglobulins, have been proposed to mediate cellular injury in TTP. However, systematic analyses of TTP patient plasma for the presence of platelet or endothelial cell antibodies are lacking. We, therefore, analyzed 48 TTP patient plasma samples for the presence of platelet and endothelial cell antibodies by using enzyme‐linked immunosorbent assay, flow cytometry, and microlymphocytotoxicity. Twelve of 48 TTP patient samples (25%) reacted against purified platelet glycoproteins. Nine (19%) also contained antibodies that bound to allogeneic target platelets in flow‐cytometric assays. Nine of 48 samples (19%) contained antibodies to human umbilical vein endothelial cells in flow‐cytometric assays, and seven of 48 patient samples (15%) bound to human dermal microvascular endothelial cells. Six of 48 (13%) patient plasma samples contained antibodies that bound to human umbilical vein endothelial cells activated with γ‐interferon and tumor necrosis factor‐α. Of twenty samples that were reactive in one or more platelet or endothelial cell assay, eight contained human leukocyte antigen antibodies reactive in microlymphocytotoxicity. These studies demonstrate that antibodies reactive against platelet or endothelial cell antigens are not prevalent in TTP, and that more than a third of antibodies detected are human leukocyte antigen alloantibodies. Our findings suggest that autoantibodies against platelets or endothelial cells are not important in the pathogenesis of this syndrome. Am. J. Hematol. 62:82–87, 1999. © 1999 Wiley‐Liss, Inc.</description><subject>antibody</subject><subject>Autoantibodies - blood</subject><subject>Biological and medical sciences</subject><subject>Blood Platelets - immunology</subject><subject>Cells, Cultured</subject><subject>Cytotoxicity, Immunologic</subject><subject>endothelial cell</subject><subject>Endothelium, Vascular - immunology</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Flow Cytometry</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Humans</subject><subject>Immunoglobulin G - immunology</subject><subject>Immunoglobulin M - immunology</subject><subject>Medical sciences</subject><subject>platelet</subject><subject>Platelet diseases and coagulopathies</subject><subject>Platelet Membrane Glycoproteins - immunology</subject><subject>Purpura, Thrombotic Thrombocytopenic - blood</subject><subject>Purpura, Thrombotic Thrombocytopenic - immunology</subject><subject>thrombotic thrombocytopenic purpura</subject><subject>Umbilical Veins</subject><issn>0361-8609</issn><issn>1096-8652</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UV2L1DAUDaK44-pfkD6I7D50vEnaNJkVYRg_ZmRlHlafQ5rcspFMW5vOyvx7U2d0BUUI5H4cTk7OIeSKwpwCsFcXN5vV5pKCErkUJbugSikKl4It2GvJFovl5m2-_Ljmb_gc5qvtFcvXD8jsN_4hmQEXNNWgzsiTGL8CUFpIeEzOKJSgUjsj4ZNv_c6EDO-8w9Zi1jVZH8yIAcfMtC7D1nXjLQafQBZDyAY0dvR3mLajrzvnMWa-zcbbodvV3ejtr9Iexq7HNg36_ZCOeUoeNSZEfHa6z8mX9-8-r9b59fbDZrW8zm0hOM95XXOHpSgVpY5WsnCMSQMNssbKohEVU1UphQA0vOA0yTHcOagUk1ixkvNz8vLI2w_dtz3GUe98nLSbFrt91BVIqICyBLw5Au3QxThgo_shuTEcNAU9haD1FIKeTNWTqfoYghZMMy3TOoWgpxA016BX2zRdJ9bnp-f39Q7dH5xH1xPgxQlgojWhGUxrfbzHpe9xoe7VffcBD39J-7-yfwj72fMfQXCvCw</recordid><startdate>199910</startdate><enddate>199910</enddate><creator>Raife, Thomas J.</creator><creator>Atkinson, Bonnie</creator><creator>Aster, Richard H.</creator><creator>McFarland, Janice G.</creator><creator>Gottschall, Jerome L.</creator><general>John Wiley & Sons, Inc</general><general>Wiley-Liss</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>7X8</scope></search><sort><creationdate>199910</creationdate><title>Minimal evidence of platelet and endothelial cell reactive antibodies in thrombotic thrombocytopenic purpura</title><author>Raife, Thomas J. ; Atkinson, Bonnie ; Aster, Richard H. ; McFarland, Janice G. ; Gottschall, Jerome L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4633-3bb3de565911d1784d228a0fe2fc84f6729758660ea3431eaca3dd07928e72533</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>antibody</topic><topic>Autoantibodies - blood</topic><topic>Biological and medical sciences</topic><topic>Blood Platelets - immunology</topic><topic>Cells, Cultured</topic><topic>Cytotoxicity, Immunologic</topic><topic>endothelial cell</topic><topic>Endothelium, Vascular - immunology</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Flow Cytometry</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Humans</topic><topic>Immunoglobulin G - immunology</topic><topic>Immunoglobulin M - immunology</topic><topic>Medical sciences</topic><topic>platelet</topic><topic>Platelet diseases and coagulopathies</topic><topic>Platelet Membrane Glycoproteins - immunology</topic><topic>Purpura, Thrombotic Thrombocytopenic - blood</topic><topic>Purpura, Thrombotic Thrombocytopenic - immunology</topic><topic>thrombotic thrombocytopenic purpura</topic><topic>Umbilical Veins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Raife, Thomas J.</creatorcontrib><creatorcontrib>Atkinson, Bonnie</creatorcontrib><creatorcontrib>Aster, Richard H.</creatorcontrib><creatorcontrib>McFarland, Janice G.</creatorcontrib><creatorcontrib>Gottschall, Jerome L.</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>MEDLINE - Academic</collection><jtitle>American journal of hematology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Raife, Thomas J.</au><au>Atkinson, Bonnie</au><au>Aster, Richard H.</au><au>McFarland, Janice G.</au><au>Gottschall, Jerome L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Minimal evidence of platelet and endothelial cell reactive antibodies in thrombotic thrombocytopenic purpura</atitle><jtitle>American journal of hematology</jtitle><addtitle>Am J Hematol</addtitle><date>1999-10</date><risdate>1999</risdate><volume>62</volume><issue>2</issue><spage>82</spage><epage>87</epage><pages>82-87</pages><issn>0361-8609</issn><eissn>1096-8652</eissn><coden>AJHEDD</coden><abstract>Thrombotic thrombocytopenic purpura (TTP) is a syndrome characterized by microvascular thrombosis with thrombocytopenia and end‐organ injury. Evidence suggests that platelet or endothelial cell injury may be initial pathological events in TTP. A number of factors in patient plasma, including immunoglobulins, have been proposed to mediate cellular injury in TTP. However, systematic analyses of TTP patient plasma for the presence of platelet or endothelial cell antibodies are lacking. We, therefore, analyzed 48 TTP patient plasma samples for the presence of platelet and endothelial cell antibodies by using enzyme‐linked immunosorbent assay, flow cytometry, and microlymphocytotoxicity. Twelve of 48 TTP patient samples (25%) reacted against purified platelet glycoproteins. Nine (19%) also contained antibodies that bound to allogeneic target platelets in flow‐cytometric assays. Nine of 48 samples (19%) contained antibodies to human umbilical vein endothelial cells in flow‐cytometric assays, and seven of 48 patient samples (15%) bound to human dermal microvascular endothelial cells. Six of 48 (13%) patient plasma samples contained antibodies that bound to human umbilical vein endothelial cells activated with γ‐interferon and tumor necrosis factor‐α. Of twenty samples that were reactive in one or more platelet or endothelial cell assay, eight contained human leukocyte antigen antibodies reactive in microlymphocytotoxicity. These studies demonstrate that antibodies reactive against platelet or endothelial cell antigens are not prevalent in TTP, and that more than a third of antibodies detected are human leukocyte antigen alloantibodies. Our findings suggest that autoantibodies against platelets or endothelial cells are not important in the pathogenesis of this syndrome. Am. J. Hematol. 62:82–87, 1999. © 1999 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>John Wiley & Sons, Inc</pub><pmid>10509001</pmid><doi>10.1002/(SICI)1096-8652(199910)62:2<82::AID-AJH3>3.0.CO;2-H</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | antibody Autoantibodies - blood Biological and medical sciences Blood Platelets - immunology Cells, Cultured Cytotoxicity, Immunologic endothelial cell Endothelium, Vascular - immunology Enzyme-Linked Immunosorbent Assay Flow Cytometry Hematologic and hematopoietic diseases Humans Immunoglobulin G - immunology Immunoglobulin M - immunology Medical sciences platelet Platelet diseases and coagulopathies Platelet Membrane Glycoproteins - immunology Purpura, Thrombotic Thrombocytopenic - blood Purpura, Thrombotic Thrombocytopenic - immunology thrombotic thrombocytopenic purpura Umbilical Veins |
title | Minimal evidence of platelet and endothelial cell reactive antibodies in thrombotic thrombocytopenic purpura |
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